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Pregnancy as a period of risk, adaptation, and resilience for mothers and infants

Published online by Cambridge University Press:  11 January 2021

Elysia Poggi Davis*
Affiliation:
Department of Psychology, University of Denver, Denver, CO, USA Department of Psychiatry and Human Behavior, University of California, Irvine, CA, USA
Angela J. Narayan
Affiliation:
Department of Psychology, University of Denver, Denver, CO, USA
*
Author for Correspondence: Elysia Davis, Department of Psychology, University of Denver, Denver, CO, USA; E-mail: Elysia.Davis@du.edu.
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Abstract

The pregnancy period represents a unique window of opportunity to identify risks to both the fetus and mother and to deter the intergenerational transmission of adversity and mental health problems. Although the maternal–fetal dyad is especially vulnerable to the effects of stress during pregnancy, less is known about how the dyad is also receptive to salutary, resilience-promoting influences. The present review adopts life span and intergenerational perspectives to review four key areas of research. The first part describes how pregnancy is a sensitive period for both the mother and fetus. In the second part, the focus is on antecedents of maternal prenatal risks pertaining to prenatal stress response systems and mental health. The third part then turns to elucidating how these alterations in prenatal stress physiology and mental health problems may affect infant and child outcomes. The fourth part underscores how pregnancy is also a time of heightened fetal receptivity to maternal and environmental signals, with profound implications for adaptation. This section also reviews empirical evidence of promotive and protective factors that buffer the mother and fetus from developmental and adaptational problems and covers a sample of rigorous evidence-based prenatal interventions that prevent maladaptation in the maternal–fetal dyad before babies are born. Finally, recommendations elaborate on how to further strengthen understanding of pregnancy as a period of multilevel risk and resilience, enhance comprehensive prenatal screening, and expand on prenatal interventions to promote maternal–fetal adaptation before birth.

Type
Special Section 1: 2019 Minnesota Symposium on Child Psychology
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2020. Published by Cambridge University Press

The prenatal period is a time of rapid development, when a multitude of psychological and physiological changes occur for both mother and fetus. Thus, pregnancy is a sensitive period when the dyad is vulnerable to the effects of adversity; however, mothers and infants also are especially receptive to salutary influences. Research has found that maternal exposure to adversity prior to conception (particularly during her childhood) can have transformative neurobiological and epigenetic effects that may be biologically embedded and transmitted to the fetus (Swales et al., Reference Swales, Stout-Oswald, Glynn, Sandman, Wing and Davis2018; Yehuda & Meaney, Reference Yehuda and Meaney2018). Compared to women without early-life adversity and mental health problems prior to pregnancy, pregnant women with a history of adversity and mental health problems may experience more risks to their mental health and more disruptions to their prenatal stress physiology. Therefore, their offspring may be at higher risk for developmental problems in the domains of stress regulation, mental health, cognitive development, and relationship formation (Sperlich & Seng, Reference Sperlich and Seng2008; Yehuda & Meaney, Reference Yehuda and Meaney2018). In contrast, women's positive early-life experiences from childhood may be a source of strength and resilience and may have promotive and protective benefits for maternal and infant outcomes. Prenatal stress, mental health, and maternal wellbeing during pregnancy may therefore represent an important link between maternal early-life experiences and maternal and fetal health.

The present review focuses on the intergenerational transmission of risk and resilience during the pregnancy period, with a focus on understanding (a) antecedents of maternal prenatal mental health problems and stress rooted in maternal lifetime adversity, and (b) consequences of maternal mental health problems and stress on offspring outcomes. In this review, prenatal stress includes perceptions of stress as well as stress physiology, and mental health problems during pregnancy include depression, generalized anxiety (hereinafter referred to as anxiety) and post-traumatic stress disorder (PTSD). We focus on these three mental health problems because of their common occurrence in pregnant women, the increasing body of research specifically linking them to alterations in stress physiology during pregnancy, and the evidence that when these disorders occur during pregnancy, they are associated with fetal development.

In the United States, compared to non-pregnant women, pregnant women may experience twice the rate of depression (up to 20% vs. 10%; Center for Disease Control and Prevention (CDC), 2019b), and low-income pregnant women may experience more than three-fold rates of depression (approximately 30% to 50% vs. 10%: Choi & Sikkema, Reference Choi and Sikkema2016; Narayan et al., Reference Narayan, Rivera, Bernstein, Castro, Gantt, Thomas and Lieberman2017). Although more difficult to distinguish due to normative fears concerning pregnancy and childbirth, rates of prenatal anxiety also are higher compared to non-pregnant women (Dunkel Schetter & Tanner, Reference Dunkel Schetter and Tanner2012). Rates of PTSD, a less-studied prenatal mental health problem than depression and anxiety but an especially potent risk for women with childhood adversity, are also elevated in community samples of pregnant women compared to their non-pregnant counterparts (e.g., approximately 6%–8% compared to 4%–5%; Seng, Rauch, et al., Reference Seng, Rauch, Resnick, Reed, King, Low and Liberzon2010). In lower-income samples, PTSD symptoms may be clinically elevated in as many as 18%–29% of pregnant women or more, particularly if women are high-risk due to childhood adversity and pregnancy complications (Narayan et al., Reference Narayan, Rivera, Bernstein, Castro, Gantt, Thomas and Lieberman2017; Narayan, Atzl, et al., Reference Narayan, Atzl, Merrick, River and Peña2019; Yildiz, Ayers, & Phillips, Reference Yildiz, Ayers and Phillips2017). Many reasons may account for heightened rates of mental health problems during pregnancy. These include factors associated with the pregnancy (e.g., whether it was planned or wanted), support in the co-parenting relationship (e.g., whether the father of the baby provides support and wants the pregnancy), demographic and financial circumstances (e.g. socioeconomic status, access to concrete needs, number of children already in the family), and other emotional, and cognitive factors that may influence pregnant women's well-being (Narayan et al., 2019; Slade, Cohen, Sadler, & Miller, Reference Slade, Cohen, Sadler, Miller and Zeanah2009; Sperlich & Seng, Reference Sperlich and Seng2008). Physiologically, the massive hormonal changes that occur normatively during the prenatal period may also unmask vulnerabilities in both physical (e.g., diabetes, hypertension) and mental (e.g., depression) health.

With a focus on mental health and stress during pregnancy, the current review synthesizes research that underscores pregnancy as a transformative opportunity to (a) understand how maternal mental health and stress lie at the intersection of mothers’ and infants’ well-being, and (b) harness and leverage resilience process to deter intergenerational transmission of stress and psychopathology in the next generation. In addition to a period of vulnerability when maternal mental health and stress may be exacerbated, pregnancy also is a window of possibility to nurture better mental health and promote recovery (Davis, Hankin, Swales, & Hoffman, Reference Davis, Hankin, Swales and Hoffman2018; Garcia et al., Reference Garcia, Valente, Lillehei, Grote, Hankin and Davis2019; Narayan, Rivera, Bernstein, Harris, & Lieberman, Reference Narayan, Rivera, Bernstein, Harris and Lieberman2018). Many women are motivated by the upcoming birth of a new child and optimistic for change. Women also typically have more contact with the medical system during their pregnancies, so there is greater opportunity for outreach and treatment (Davis et al., Reference Davis, Hankin, Swales and Hoffman2018; Narayan et al., Reference Narayan, Rivera, Bernstein, Castro, Gantt, Thomas and Lieberman2017; River, Narayan, Galvan et al., Reference River, Narayan, Galvan, Rivera, Harris and Lieberman2019). Finally, empirical evidence points to increased plasticity in the maternal as well as the fetal brain during the prenatal period (Davis et al., Reference Davis, Hankin, Glynn, Head, Kim and Sandman2019; Glynn, Reference Glynn2010, Reference Glynn2012; Glynn, Davis, Sandman, & Goldberg, Reference Glynn, Davis, Sandman and Goldberg2016). For these reasons, understanding the antecedents and consequences of maternal mental health and stress during the prenatal period and applying life span and intergenerational perspectives are important for identifying opportunities for prevention and intervention to promote resilience.

This review is structured in four parts. The first section will provide an overview of the prenatal period as a sensitive period of development for both the fetus and the mother. The second section will focus on experiences of adversity that may be antecedents of maternal stress and mental health problems during the prenatal period. The scope of adversity includes childhood adversity, such as maltreatment and broader adverse childhood experiences (ACEs), which, in addition to maltreatment, include exposure to family/household dysfunction (i.e., parental divorce/separation, domestic violence, substance use, mental illness, and incarceration; CDC, 2019a; Felitti et al., Reference Felitti, Anda, Nordenberg, Williamson, Spitz, Edwards and Marks1998); and adulthood adversity, such as adulthood life stressors, and intimate partner violence (IPV) or other relationship conflict. The third section of the review will focus on prenatal maternal stress and mental health in relation to offspring development. The fourth section will focus on adaptation and resilience during the pregnancy period. Here, we present evidence that because maternal stress and mental health problems during pregnancy are strongly associated with fetal development, the signals that the fetus receives in the prenatal environment may promote adaptation to the postnatal world and also may be beneficial for development, growth, and survival. Finally, we discuss research and translational efforts to identify and promote resilience during the pregnancy period, arguing that pregnancy is a prime opportunity for prevention and intervention efforts designed to benefit maternal mental health and promote fetal infant development and wellbeing.

Pregnancy as a Sensitive Period for the Fetus and Mother: Biological Changes

Fetal development

The pace of fetal development far exceeds development during any other period of the life span. The dramatic transformation from a single-celled zygote to a newborn involves the formation and maturation of all major organ systems. The carefully orchestrated series of events that underlie the development of the brain are particularly complex. Brain development begins during gestation and continues into the postnatal period (Gilmore, Knickmeyer, & Gao, Reference Gilmore, Knickmeyer and Gao2018). The pace of fetal brain maturation is particularly rapid. Neurogenesis commences as early as 42 days after conception (Stiles & Jernigan, Reference Stiles and Jernigan2010) and by the end of the second trimester, 200 billion neurons have been produced (Bourgeois, Reference Bourgeois1997). Cells migrate to their final destination where they begin to arborize and form dendritic branches (Sidman & Rakic, Reference Sidman and Rakic1973). Synaptogenesis is present as early as the 16th gestational week, indicating communication between neurons (Bourgeois, Goldman-Rakic, & Rakic, Reference Bourgeois, Goldman-Rakic and Rakic1994; Kostović, Judas, Rados, & Hrabac, Reference Kostović, Judas, Rados and Hrabac2002).

Although genetic factors clearly play a central role in these maturational processes, it has become increasingly clear that environmental factors, including fetal experiences and exposures in utero, also play a critical role in shaping these developmental processes. The prenatal period is a sensitive period when the fetus is particularly susceptible to environmental influences. Experiences during the prenatal period are critical for normative processes from the closing of the neural tube to development of circuits involved in sensory processing (Burton, Hempstock, & Jauniaux, Reference Burton, Hempstock and Jauniaux2001; Godfrey & Barker, Reference Godfrey and Barker2001; Moon & Fifer, Reference Moon and Fifer2000). The developing fetal brain additionally is particularly susceptible to harm from teratogenic factors such as toxins, infection, maternal stress including prenatal mental health problems, and other environmental exposures (Davis, Head, Buss, & Sandman Reference Davis, Head, Buss and Sandman2017; Davis et al., Reference Davis, Hankin, Glynn, Head, Kim and Sandman2019; Kim et al., Reference Kim, Davis, Sandman, Sporns, O'Donnell, Buss and Hetrick2017; Madigan et al., Reference Madigan, Oatley, Racine, Fearon, Schumacher, Akbari and Tarabulsy2018). Less considered is the likelihood that the fetal period is also a window of opportunity when salutary experiences may exert beneficial influences. Understanding the influence of prenatal experiences, both adverse and salutary, on fetal brain development is critical because it then allows us to investigate individual differences in infants’ emotional and cognitive development and their subsequent vulnerability and resilience to mental health problems.

Maternal development

Women also undergo many changes during pregnancy. Vast physiological changes support fetal growth and development but also change the maternal brain in preparation for motherhood. During gestation, maternal physiology undergoes massive changes including transformations in stress physiology and immune function, both of which likely have implications for the maternal brain (Howland, Sandman, & Glynn, Reference Howland, Sandman and Glynn2017; Noroña, Doom, Davis, & Gunnar, Reference Noroña, Doom, Davis, Gunnar, Rubenstein and Rakic2020). For the mother, the hormonal changes of pregnancy are perhaps more dramatic than any other phase of the life span. A robust non-human animal literature documents that the experience of pregnancy is associated with neurological changes in the mother that persist throughout her life span (see Glynn et al., Reference Glynn, Howland, Sandman, Davis, Phelan and Baram2018 for review). The hormone changes associated with gestation are linked to changes in neuronal structure, signaling, and neurogenesis (Keyser-Marcus et al., Reference Keyser-Marcus, Stafisso-Sandoz, Gerecke, Jasnow, Nightingale, Lambert and Kinsley2001; Shingo et al., Reference Shingo, Gregg, Enwere, Fujikawa, Hassam, Geary and Weiss2003). Further, normative increases in pregnancy-related hormones (e.g., estrogen) not only predict maternal behavior, but experimental administration of them also elicits the onset of maternal behavior in virgin animals (Fahrbach & Pfaff, Reference Fahrbach and Pfaff1986; Numan, Reference Numan2006; Numan, Rosenblatt, & Komisaruk, Reference Numan, Rosenblatt and Komisaruk1977). The impact of pregnancy on the female goes beyond behaviors and neural circuits directly linked to mothering. The experience of gestation also is linked to consistent alterations in both physiological and psychological stress responses.

The hypothalamic–pituitary–adrenocortical (HPA) axis undergoes profound changes during the prenatal period. The HPA axis is one of the major stress responsive systems and plays a central role in maintaining homeostasis. During the prenatal period the HPA axis plays a key role in regulation of fetal maturation and timing of delivery and directly impacts the maternal brain (Howland et al., Reference Howland, Sandman and Glynn2017; Smith, Mesiano, & McGrath, Reference Smith, Mesiano and McGrath2002). In response to stress signals, corticotropin releasing hormone (CRH) is released from the hypothalamus. CRH binds to receptors in the pituitary leading to the production of proopiomelanocortin (POMC) which is cleaved by enzymes into adrenocorticotrophic hormone (ACTH) and other bioactive peptides. ACTH is released into the bloodstream and stimulates secretion of the glucocorticoid, cortisol, from the adrenal cortex. This system is regulated by a negative feedback loop whereby the release of cortisol feeds back to the hypothalamus and pituitary decreasing the production of CRH and ACTH. This cascade of hormones mobilizes resources to cope with stress and maintain homeostasis. During pregnancy the development of the placenta transforms the regulation of this system. The placenta, a fetal organ, produces hormones including CRH in both the maternal and fetal systems (King, Nicholson, & Smith, Reference King, Nicholson and Smith2001). The CRH produced from the placenta is identical in structure and bioactivity to CRH produced from the hypothalamus (Goland, Reference Goland1988). However, in contrast to the negative feedback at the level of the hypothalamus, cortisol stimulates the production of CRH from the placenta, similar to the role of cortisol in the amygdala (Robinson, Emanuel, Frim, & Majzoub, Reference Robinson, Emanuel, Frim and Majzoub1988). Therefore, during pregnancy, there is a positive feedback loop whereby both maternal and fetal cortisol stimulate an increase in the production of CRH from the placenta (Sandman et al., Reference Sandman, Glynn, Schetter, Wadhwa, Garite, Chicz-DeMet and Hobel2006; Waffarn & Davis, Reference Waffarn and Davis2012). This HPA and placental axis represents a pathway by which environmental signals may be transmitted to the fetus and thus, shape its developmental course. During pregnancy, the maternal pituitary gland doubles in size, and cortisol levels increase 3- to 5-fold over gestation, achieving levels typically only seen in Cushing's disease (Mastorakos & Ilias, Reference Mastorakos and Ilias2003; Sandman et al., Reference Sandman, Glynn, Schetter, Wadhwa, Garite, Chicz-DeMet and Hobel2006). Placental CRH production in the maternal circulation increases 40-fold from the end of the first trimester to term (Sandman et al., Reference Sandman, Glynn, Schetter, Wadhwa, Garite, Chicz-DeMet and Hobel2006; Sandman, Glynn, & Davis, Reference Sandman, Glynn, Davis, Kisilevsky and Reissland2015).

These massive changes in maternal HPA axis functioning during the prenatal period are normative and support maturation of the fetus as well as timing of parturition, but also may affect maternal mental health during the perinatal period (Glynn, Reference Glynn2010). During pregnancy, the HPA axis response to a variety of different stressors diminishes (de Weerth & Buitelaar, Reference de Weerth and Buitelaar2005). Further and in parallel to physiological changes, pregnant women also exhibit reduced psychological responses to stress (Glynn, Wadhwa, Dunkel Schetter, & Sandman, Reference Glynn, Wadhwa, Dunkel Schetter and Sandman2001, Reference Glynn, Schetter, Wadhwa and Sandman2004).These normative responses are likely adaptive and may provide some protection to the mother–fetal dyad during pregnancy. However, elevated exposure to stressors, especially early in gestation, increase risk for preterm birth (Glynn et al., Reference Glynn, Wadhwa, Dunkel Schetter and Sandman2001). Moreover, women who do not show the normative decrease in physiological and psychological stress responding during pregnancy are at increased risk for preterm delivery (Buss, Entringer, et al., Reference Buss, Entringer, Reyes, Chicz-DeMet, Sandman, Waffarn and Wadhwa2009; Glynn, Dunkel Schetter, Hobel, & Sandman, Reference Glynn, Dunkel Schetter, Hobel and Sandman2008). The endocrine profile in pregnancy also may impact maternal sensitivity to stressors, thereby contributing to vulnerability to mental health problems during the perinatal period (Glynn, Davis, & Sandman, Reference Glynn, Davis and Sandman2013). Prenatal stress exposure additionally increases risk for development of maternal anxiety and mood disorders (Slattery & Hillerer, Reference Slattery and Hillerer2016). Prenatal hormone trajectories of the HPA and placental axis have been proposed to be one of the risk indicators for the development of postpartum depression (Glynn et al., Reference Glynn, Davis and Sandman2013; Glynn & Sandman, Reference Glynn and Sandman2014; Yim et al., Reference Yim, Glynn, Dunkel-Schetter, Hobel, Chicz-DeMet and Sandman2009, Reference Yim, Glynn, Schetter, Hobel, Chicz-Demet and Sandman2010). This evidence suggests that prenatal maternal stress physiology and mental health problems during pregnancy are closely interrelated, with stress physiology potentially affecting the emergence of mental health problems, and pre-conception and prenatal mental health problems affecting stress physiology. For instance, elevated maternal PTSD symptoms during pregnancy affect cortisol concentrations during pregnancy (Seng, Low, Ben-Ami, & Liberzon, Reference Seng, Low, Ben-Ami and Liberzon2010). Therefore, mental health problems and stress physiology during pregnancy likely have bidirectional, transactional effects on maternal well-being during pregnancy, as well as fetal well-being, and labor, delivery, and infant outcomes.

Adversity Antecedents of Prenatal Maternal Stress and Mental Health Problems

Adversity and prenatal maternal stress physiology

During pregnancy, many women reference their childhood experiences, both negative and positive, in considering how they want to care for their new baby. Negative childhood experiences, such as maltreatment and other forms of interpersonal trauma, can have enduring effects on maternal mental health problems during pregnancy and on multiple aspects of individual and maternal–fetal stress physiology. Thus, the pregnancy period may be a particularly sensitive time for women, when prior history of adversity and unresolved trauma may render pregnant women vulnerable to re-emergence of mental health problems and stress (Slade & Cohen, Reference Slade and Cohen1996; Sperlich & Seng, Reference Sperlich and Seng2008). Given the plasticity of the mother and her fetus during the prenatal period, the effects of early-life adversity may be amplified with implications for maternal and child development (Yehuda & Meaney, Reference Yehuda and Meaney2018).

Childhood adversity may contribute to maladaptive alterations in stress physiology during pregnancy, such as greater maternal HPA axis dysregulation evidenced by both elevated and suppressed concentrations of cortisol during pregnancy (Bowers & Yehuda, Reference Bowers and Yehuda2016; Schreier, Enlow, Ritz, Gennings, & Wright, Reference Schreier, Enlow, Ritz, Gennings and Wright2015; Swales et al., Reference Swales, Stout-Oswald, Glynn, Sandman, Wing and Davis2018). Maternal report of childhood maltreatment is linked to elevations in hair cortisol concentrations during pregnancy (Schreier et al., Reference Schreier, Enlow, Ritz, Gennings and Wright2015) and has been found to amplify the impact of women's more proximal exposure to adulthood traumatic events prior to pregnancy on prenatal hair cortisol concentrations (Swales et al., Reference Swales, Stout-Oswald, Glynn, Sandman, Wing and Davis2018). Further, childhood maltreatment also is associated with alterations in placental–fetal stress physiology, including significantly steeper increases in placental CRH across gestation (Buss et al., Reference Buss, Entringer, Moog, Toepfer, Fair, Simhan and Wadhwa2017; Moog et al., Reference Moog, Entringer, Rasmussen, Styner, Gilmore, Kathmann and Buss2018). These studies point to pathways by which maternal childhood adversity may directly affect fetal stress exposure and transmit higher-than-typical cortisol and placental CRH levels. The dynamic changes in maternal physiology during this period and the responsivity to stress signals suggests a pathway by which childhood adversity may alter maternal prenatal stress regulation and reactivity, and such dysregulation of stress physiology may, in turn, affect maternal–fetal stress transmission.

Both hypercortisolism and hypocortisolism during pregnancy are associated with negative consequences for maternal and fetal well-being (Bowers & Yehuda, Reference Bowers, Yehuda and Chen2020; Davis et al., Reference Davis, Head, Buss and Sandman2017; Davis & Sandman, Reference Davis and Sandman2010; Yehuda & Meaney, Reference Yehuda and Meaney2018). Depending on the nature, severity, and chronicity of the childhood adversity exposure, some pregnant women who were chronically maltreated may show hypocortisolism, a pattern observed in non-pregnant, chronically maltreated individuals (Gunnar & Quevedo, Reference Gunnar and Quevedo2007; Yehuda et al., Reference Yehuda, Flory, Pratchett, Buxbaum, Ising and Holsboer2010). This downregulation of cortisol secretion is believed to be a response to chronic elevations in cortisol and serves to protect against wear and tear on the regulatory and inflammatory systems. Downregulation of cortisol secretion, however, may increase risk that subsequent adversity will not be met with an effective stress response and may render individuals more susceptible to mental health problems, such as PTSD (Bowers & Yehuda, Reference Bowers and Yehuda2016; Pratchett & Yehuda, Reference Pratchett and Yehuda2011). Non-pregnant individuals with childhood adversity and PTSD may show blunted cortisol patterns, but it is unclear if these patterns preceded the emergence of PTSD, thereby increasing risk for it, are a direct consequence of PTSD, or are an indirect consequence from chronic or severe childhood adversity (Pratchett & Yehuda, Reference Pratchett and Yehuda2011).

Key in the pathway between maternal childhood and adulthood adversity prior to pregnancy and alterations in maternal stress physiology during pregnancy are ongoing maternal mental health problems stemming from adversity. In actuality, many studies linking maternal childhood and adulthood adversity to disruptions in stress physiology do not consider the preceding and often ongoing role of mental health problems during pregnancy, which may affect and be affected by altered stress physiology (Evans, Myers, & Monk, Reference Evans, Myers and Monk2008; Yehuda & Meaney, Reference Yehuda and Meaney2018). More research is needed in this area. Regardless, the dramatic multilevel changes during pregnancy increase the likelihood that the physiological consequences of early and cumulative adversity may be amplified during pregnancy, thereby impacting both the mother and fetus.

Adversity and prenatal maternal mental health problems

From a psychological standpoint, during pregnancy, women reflect back on their childhood as they consider the type of caregiving they had, and the type of parent they want to be. For women with histories of childhood adversity, such as maltreatment and other interpersonal trauma in their families of origin, the pregnancy period can be a time when women are haunted by unresolved traumatic experiences (Lieberman, Díaz, & Van Horn, Reference Lieberman, Díaz and Van Horn2009; Narayan, Oliver Bucio, et al., Reference Narayan, Oliver Bucio, Rivera and Lieberman2016; Slade et al., Reference Slade, Cohen, Sadler, Miller and Zeanah2009). Physical changes and physiological sensations associated with pregnancy, such as experiencing abdominal growth, the fetus kicking, and other aches and pains, can invoke reminders of past abuse and loss of control over one's body at the hands of the abuser. Some women with histories of maltreatment may experience the growing fetus as a bodily invasion that is out of their control because it reminds them of the powerlessness of being victimized (Sperlich & Seng, Reference Sperlich and Seng2008). Adulthood adversity, such as stressful and traumatic life events in adulthood, including IPV, can also amplify consequences of childhood adversity and mental health problems.

Maternal experience of childhood adversity

As women prepare to become mothers, adverse experiences with their childhood caregivers may once again become especially salient and harmful. Childhood adversity more broadly, and childhood maltreatment more specifically, is associated with elevated maternal mental health problems during pregnancy, such as elevated depression, anxiety, and PTSD symptoms (Choi & Sikkema, Reference Choi and Sikkema2016; Racine, Zumwalt, McDonald, Tough, & Madigan, Reference Racine, Zumwalt, McDonald, Tough and Madigan2019; Seng, Reference Seng2002). A few recent studies have illuminated that specific types of childhood adversity may uniquely affect specific types of maternal mental health problems during pregnancy. For instance, retrospective report of both family dysfunction and physical and emotional abuse, but not sexual abuse, was associated with psychosocial difficulties, including depression, anxiety, perceived stress, and other social risks, during pregnancy (Racine, Madigan, et al., Reference Racine, Madigan, Plamondon, McDonald and Tough2018). Of note, however, this study did not assess PTSD during pregnancy, which is a well-established consequence of childhood sexual abuse (Sperlich & Seng, Reference Sperlich and Seng2008). Another recent study found that a history of childhood maltreatment was associated with depression and PTSD symptoms during pregnancy, but exposure to childhood family or household dysfunction was not. In addition, childhood maltreatment that was specifically reported to begin in early childhood (ages 0–5), rather than later in childhood, was associated with maternal prenatal PTSD symptoms, but not with maternal prenatal depression symptoms (Atzl, Narayan, et al., Reference Atzl, Narayan, Rivera and Lieberman2019). Taken together, these findings indicate that both type and timing of childhood adversity are important to consider for specific mental health outcomes during pregnancy.

Maternal experience of adversity in adulthood and cumulative lifetime adversity

Exposure to stressful life events and negative circumstances in adulthood before conception, as well as during pregnancy, may also exacerbate prenatal maternal mental health problems. Stressful life events including interpersonal trauma (e.g., physical and sexual assaults) but also those pertaining to homelessness, incarceration, and severe poverty during pregnancy are associated with higher levels of both depression and PTSD symptoms during pregnancy (Narayan et al., Reference Narayan, Rivera, Bernstein, Harris and Lieberman2018). Women's experiences of violent trauma, such as witnessing or experiencing physical or sexual assault from a romantic partner or stranger before or during pregnancy were also robustly related to PTSD symptoms during pregnancy (Harris-Britt, Martin, Li, Casanueva, & Kupper, Reference Harris-Britt, Martin, Li, Casanueva and Kupper2004). Studies also specifically point to the relationship dysfunction with the father of the baby as a particularly influential form of adulthood adversity for mental health during pregnancy.

Romantic relationship conflict and IPV can take multiple forms (e.g., physical, sexual, and psychological), and can become a complicated risk factor for pregnant women. For instance, for some women, the pregnancy period may represent a time of decreased risk for IPV victimization because the woman and fetus are viewed a more fragile. For other women, however, it might represent a period of increased risk, especially if the pregnancy is unplanned or the perpetrator questions the paternity (Chambliss, Reference Chambliss2008; Jasinski, Reference Jasinski2004; Narayan, Hagan, Cohodes, Rivera, & Lieberman, Reference Narayan, Hagan, Cohodes, Rivera and Lieberman2016). In terms of specificity of adversity and prenatal mental health problems, studies have linked physical and psychological IPV victimization during pregnancy to women's heighted levels of prenatal depression (Flanagan, Gordon, Moore, & Stuart, Reference Flanagan, Gordon, Moore and Stuart2015).

IPV victimization is more common among women who experienced childhood maltreatment and is another factor affecting PTSD during pregnancy (Pratchett & Yehuda, Reference Pratchett and Yehuda2011; Seng, Reference Seng2002). One study found that a history of childhood maltreatment was associated with increased rates of IPV victimization during pregnancy, and both childhood maltreatment and IPV were independently associated with prenatal PTSD symptoms. Moreover, psychological IPV victimization, as opposed to physical or sexual IPV victimization, was most strongly associated with PTSD symptoms during pregnancy (Huth-Bocks, Krause, Ahlfs-Dunn, Gallagher, & Scott, Reference Huth-Bocks, Krause, Ahlfs-Dunn, Gallagher and Scott2013), again illustrating the importance of considering specificity in the type of risk in addition to the cumulative nature of childhood and adulthood risks. Moreover, relationship-based adversity may reflect victimization that has accumulated from childhood. For instance, higher levels of relationship conflict with and lower levels of support from the baby's father partially mediated the link between childhood maltreatment and both depression symptoms and PTSD symptoms during pregnancy (River, Narayan, Atzl, Rivera, & Lieberman, Reference River, Narayan, Atzl, Rivera and Lieberman2019). These latter findings emphasize the enduring role that childhood adversity likely has on prenatal maternal mental health problems. Although many of the above studies relied on retrospective report of childhood experiences, they suggest that it is critical to consider life span experiences of pregnant women, beginning in childhood in order to understand intergenerational transmission of mental health problems through the prenatal period.

The above evidence elucidates several potential life span pathways of risk characterized by cumulative adversity, the emergence of mental health problems, and alterations in stress physiology. Specifically, maternal history of childhood adversity may portend risk for subsequent exposure to adversity or revictimization, either before or during the pregnancy period, or both. Moreover, both childhood adversity and adulthood adversity likely affect mental health problems during pregnancy (Narayan et al., 2016; Pratchett & Yehuda, Reference Pratchett and Yehuda2011; Sperlich & Seng, Reference Sperlich and Seng2008). In addition, although more research is needed, maternal exposure to adversity affects both maternal mental health problems and stress physiology during pregnancy, which in turn have bidirectional effects (Evans et al., Reference Evans, Myers and Monk2008; Seng, Reference Seng2002). Together, these complicated pathways pose risks into the postpartum period in the domains of postnatal maternal mental health, infant stress regulation and responsivity, and maternal–infant bonding.

Fetal Programming: Maternal Prenatal Stress Predicts Child Mental Health Problems

Maternal stress and mental health problems during the prenatal period, as discussed in the second section, likely exert profound consequences on the developing fetus as well as on the mother. The Fetal Programming or Developmental Origins of Health and Disease (DOHaD) hypothesis posits that during sensitive Windows of fetal development, the environment can exert lasting influences on health and well-being across the life span (Barker, Reference Barker1998). This hypothesis was generated largely based on studies of in-utero nutritional deprivation (Barker, Reference Barker2002; Gluckman & Hanson, Reference Gluckman and Hanson2004). Broadly, these studies indicate that the fetus adapts its developmental course in response to prenatal signals to prepare for survival in the postnatal world. Such adaptations, however, may have a long-term cost for morbidity and mortality. Prenatal adversity is linked to reduced fetal growth and small size at birth. Furthermore, numerous epidemiological and observational studies demonstrate that small size at birth is predictive of a range of physical and mental health outcomes throughout the life span (Barker, Eriksson, Forsen, & Osmond, Reference Barker, Eriksson, Forsen and Osmond2002; Davis, Buss, et al., Reference Davis, Buss, Muftuler, Head, Hasso, Wing and Sandman2011; Kim et al., Reference Kim, Davis, Sandman, Sporns, O'Donnell, Buss and Hetrick2014). It is unlikely that small size at birth is the causal risk factor; rather, it is a marker of perturbations during the prenatal period that represent the origin of the vulnerability. These studies provide evidence that the prenatal period is a sensitive window when the fetus is particularly susceptible to environmental insults. In the sections that follow, we focus on prenatal maternal stress and mental health problems as types of prenatal adversity that impact both birth outcomes and trajectories of offspring physical and mental health. As there are many excellent reviews linking prenatal maternal psychological distress to infant, child and adolescent outcomes (Davis et al., Reference Davis, Hankin, Swales and Hoffman2018; de Weerth, Reference de Weerth2018; Madigan et al., Reference Madigan, Oatley, Racine, Fearon, Schumacher, Akbari and Tarabulsy2018; Robinson, Lahti-Pulkkinen, Heinonen, Reynolds, & Raikkonen, Reference Robinson, Lahti-Pulkkinen, Heinonen, Reynolds and Raikkonen2019; Sandman, Davis, Buss, & Glynn, Reference Sandman, Davis, Buss and Glynn2011), we only briefly overview the links between prenatal maternal mental health and child outcomes here. We then discuss these links within the framework of adaptation and resilience.

Prenatal maternal stress and mental health, and child outcomes

Prenatal maternal stress and mental health problems are associated with persisting consequences for both the mother and her offspring (Barker, Jaffee, Uher, & Maughan, Reference Barker, Jaffee, Uher and Maughan2011; Buss et al., Reference Buss, Davis, Shahbaba, Pruessner, Head and Sandman2012; Davis & Pfaff, Reference Davis and Pfaff2014; Davis & Sandman, Reference Davis and Sandman2012; Korhonen, Luoma, Salmelin, & Tamminen, Reference Korhonen, Luoma, Salmelin and Tamminen2012; O'Donnell, Glover, Barker, & O'Connor, Reference O'Donnell, Glover, Barker and O'Connor2014; Sandman, Buss, Head, & Davis, Reference Sandman, Buss, Head and Davis2015). Several recent meta-analyses provide strong evidence that prenatal maternal depression is associated with preterm birth (Grigoriadis et al., Reference Grigoriadis, VonderPorten, Mamisashvili, Tomlinson, Dennis, Koren and Ross2013; Grote et al., Reference Grote, Bridge, Gavin, Melville, Iyengar and Katon2010) and low birth weight (Grote et al., Reference Grote, Bridge, Gavin, Melville, Iyengar and Katon2010). Further, maternal prenatal PTSD may additionally predict negative birth outcomes including disrupted growth and shorter gestation/increased risk for preterm birth (Cook, Ayers, & Horsch, Reference Cook, Ayers and Horsch2018). A recent prospective study of 4,408 pregnancies found that prenatal PTSD predicted increased rates of preterm birth. It is widely known that shortened gestation impacts brain development (e.g., Davis, Buss, et al., Reference Davis, Buss, Muftuler, Head, Hasso, Wing and Sandman2011; Kim et al., Reference Kim, Davis, Sandman, Sporns, O'Donnell, Buss and Hetrick2014). Interestingly, fetuses that go on to be delivered preterm display reduced connectional integrity as compared to age-matched fetuses who are delivered at term (Thomason et al., Reference Thomason, Scheinost, Manning, Grove, Hect, Marshall and Romero2017). The detection of connectivity differences among at-risk fetuses prior to birth suggests that the fetal brain is susceptible to prenatal influences and that the long-term developmental consequences of preterm birth begin in utero.

The link between prenatal maternal stress and mental health problems on development persists throughout infancy and childhood, and likely into adulthood. Most research in this area has focused on prenatal maternal stress, anxiety, and depression, with one of the most well-replicated consequences of these prenatal maternal mental health problems being increased negative emotionality in offspring. Although shared genes between the mother and her offspring clearly contribute to shared variance in mental health, evidence from studies of invitro fertilization or quasi-experimental natural disaster research suggests that environmental factors additionally contribute to the intergenerational transmission of mental health problems (Glynn et al., Reference Glynn, Wadhwa, Dunkel Schetter and Sandman2001; King & Laplante, Reference King and Laplante2005; Rice et al., Reference Rice, Harold, Boivin, Hay, van den Bree and Thapar2009). Prospective longitudinal studies show that prenatal maternal mental health problems and stress predict greater negative emotionality and fearful temperament in the offspring, assessed by both laboratory observation and maternal report (Blair, Glynn, Sandman, & Davis, Reference Blair, Glynn, Sandman and Davis2011; Davis et al., Reference Davis, Snidman, Wadhwa, Dunkel Schetter, Glynn and Sandman2004, Reference Davis, Glynn, Schetter, Hobel, Chicz-Demet and Sandman2007; Huot, Brennan, Stowe, Plotsky, & Walker, Reference Huot, Brennan, Stowe, Plotsky and Walker2004; Rouse & Goodman, Reference Rouse and Goodman2014). Further, these links are not fully accounted for by postnatal exposures, as these associations remain after covarying for postnatal factors, such as maternal postpartum mental health.

The link between prenatal maternal mental health problems, stress, and child negative emotionality persists throughout childhood and is associated with the development of children's internalizing problems (Davis & Sandman, Reference Davis and Sandman2012; Howland, Sandman, Glynn, Crippen, & Davis, Reference Howland, Sandman, Glynn, Crippen and Davis2016). A recent prospective study with close to 2,000 mother–child dyads measured maternal stress, anxiety, and depression both during pregnancy and postnatally and showed that prenatal distress predicted child negative emotionality at 3 years and internalizing problems at 5 years after covarying postnatal maternal mental health (Hentges, Graham, Plamondon, Tough, & Madigan, Reference Hentges, Graham, Plamondon, Tough and Madigan2019). Prenatal maternal stress, anxiety, and depression also predicted elevated depressive symptoms in adolescence assessed by both maternal report and child self-report (Davis et al., Reference Davis, Hankin, Glynn, Head, Kim and Sandman2019; O'Donnell et al., Reference O'Donnell, Glover, Barker and O'Connor2014). The link between prenatal maternal mental health problems and offspring internalizing psychopathology is also apparent in young adulthood, as documented in several large cohort studies (Capron et al., Reference Capron, Glover, Pearson, Evans, O'Connor, Stein and Ramchandani2015; Pearson et al., Reference Pearson, Evans, Kounali, Lewis, Heron, Ramchandani and Stein2013; Plant, Pariante, Sharp, & Pawlby, Reference Plant, Pariante, Sharp and Pawlby2015). In one study, offspring were 3.4 times more likely to have a diagnosed depressive disorder at 18–25 years of age after accounting for postnatal maternal depression and sociodemographic risk factors (Plant et al., Reference Plant, Pariante, Sharp and Pawlby2015).

Prenatal maternal stress and mental health problems additionally predict child cognitive outcomes. These include associations with general cognitive function (Davis & Sandman, Reference Davis and Sandman2010) and perhaps more specifically with executive function (Buss, Davis, et al., Reference Buss, Davis, Class, Gierczak, Pattillo, Glynn and Sandman2009; Davis & Sandman, Reference Davis and Sandman2010). Findings from two large cohort studies (Avon Longitudinal Study of Parents and Children and Generation R) show that prenatal maternal depression predicted child attentional problems at 3 years of age after covarying for both postpartum maternal depression and paternal depression (Van Batenburg-Eddes et al., Reference Van Batenburg-Eddes, Brion, Henrichs, Jaddoe, Hofman, Verhulst and Tiemeier2013). Relatedly, prenatal maternal depression predicted problems with executive functioning and attention shifting at 4 years of age (El Marroun et al., Reference El Marroun, White, Fernandez, Jaddoe, Verhulst, Stricker and Tiemeier2017) as well as increased risk for an ADHD diagnosis during childhood (Clemens et al., Reference Clemens, Castro, Blumenthal, Rosenfield, Murphy, Fava and Robinson2015). Additional prospective longitudinal studies have linked prenatal maternal anxiety to problems with attentional control through adolescence (Van den Bergh & Marcoen, Reference Van den Bergh and Marcoen2004; Van den Bergh et al., Reference Van den Bergh, Mennes, Oosterlaan, Stevens, Stiers, Marcoen and Lagae2005). These studies provide evidence for an association between prenatal maternal depression and child cognitive function.

Fetal programming of HPA axis development is one of the most frequently proposed pathways by which maternal stress and mental health are thought to impact child outcomes. Prenatal maternal stress, anxiety, and depression are linked to disruptions in children's stress responses and circadian HPA axis functioning from the neonatal period through adolescence (Davis, Glynn, Waffarn, & Sandman, Reference Davis, Glynn, Waffarn and Sandman2011; Galbally, van Rossum, Watson, de Kloet, & Lewis, Reference Galbally, van Rossum, Watson, de Kloet and Lewis2019; O'Donnell et al., Reference O'Donnell, Glover, Jenkins, Browne, Ben-Shlomo, Golding and O'Connor2013; Van den Bergh, Van Calster, Smits, Van Huffel, & Lagae, Reference Van den Bergh, Van Calster, Smits, Van Huffel and Lagae2008). For example, maternal stress during the prenatal period is associated with prolonged neonatal cortisol responses to stress (Davis, Glynn, et al., Reference Davis, Glynn, Waffarn and Sandman2011) and prenatal maternal depression predicted heightened cortisol reactivity at 1 year of age (Osborne et al., Reference Osborne, Biaggi, Chua, Du Preez, Hazelgrove, Nikkheslat and Pariante2018).

Fewer studies have evaluated the relation between maternal PTSD during pregnancy and child outcomes (Cook et al., Reference Cook, Ayers and Horsch2018; Seng, Low, Sperlich, Ronis, & Liberzon, Reference Seng, Low, Sperlich, Ronis and Liberzon2011). However, some investigators have documented that maternal PTSD during pregnancy predicts poorer infant birth outcomes, lower maternal–infant bonding, and higher levels of infant distress (Seng, Reference Seng2002; Seng et al., Reference Seng, Sperlich, Low, Ronis, Muzik and Liberzon2013). Moreover, like depression, maternal PTSD during pregnancy also is associated with shorter gestation and lower infant birth weight (Seng et al., Reference Seng, Low, Sperlich, Ronis and Liberzon2011). In terms of associations with stress physiology, following the 911 attacks, Yehuda et al. (Reference Yehuda, Engel, Brand, Seckle, Marcus and Berkowitz2005) reported that mothers who developed PTSD had lower salivary cortisol levels, as did their infants. Furthermore, lower levels of salivary cortisol in infants were subsequently associated with higher levels of infants’ distress (Brand, Engel, Canfield, & Yehuda, Reference Brand, Engel, Canfield and Yehuda2006). In another study, infants born to women who were pregnant during and then developed PTSD in response to an earthquake in Wenchuan County of Sichuan Province in China showed impairments in cognitive development (Cai et al., Reference Cai, Zhu, Sun, Qi, Xing, Zhao and Li2017). Consistent with observational human data, a mouse model of prenatal traumatic experiences showed that prenatal exposure caused an increase in anxiety-like behavior in the offspring (Osborne et al., Reference Osborne, Biaggi, Chua, Du Preez, Hazelgrove, Nikkheslat and Pariante2018). Although the extant literature provides compelling evidence that maternal stress, anxiety, and depression during the prenatal period predict stress regulatory physiology in offspring and their developmental outcomes, more attention is needed to the specific the impact of maternal PTSD during pregnancy on child outcomes, particularly child cognition.

More studies that adopt a fully intergenerational design and link maternal and child functioning through factors during the prenatal period are also needed. For example, maternal childhood adversity or adulthood adversity prior to pregnancy likely impacts developmental outcomes in the offspring via prenatal maternal stress and mental health, yet few studies have directly documented this possibility. McDonnell and Valentino (Reference McDonnell and Valentino2016) found that maternal self-report of childhood adversity predicted both prenatal maternal depression symptoms and poorer infant socioemotional functioning, suggesting that prenatal factors may contribute to the link between maternal adversity and child outcomes. Further in a sample of 907 dyads, Letourneau et al. (Reference Letourneau, Dewey, Kaplan, Ntanda, Novick, Thomas and Giesbrecht2019) showed that the relation between maternal ACEs and child internalizing and externalizing problems was partially mediated by prenatal maternal anxiety and depression. In addition, maternal report of ACEs predicted lower levels of infant adaptive functioning (e.g., motor, communication, and problem-solving skills) at 12 months via both maternal physical and mental health problems during the prenatal period (Racine, Plamondon, et al. Reference Racine, Plamondon, Madigan, McDonald and Tough2018). These findings illustrate intergenerational pathways of risk from women's experiences to infants’ development through the pregnancy period.

Adaptation and Resilience

In addition to a sensitive period of vulnerability, the pregnancy period is a window to promote adaptation and resilience in mothers and infants. Opportunities to better understand how to deter intergenerational transmission of risk include (a) identifying how maternal and environmental signals provide information to the fetus and program expectations about postnatal conditions that may promote offspring adaptation, (b) examining how links between mothers’ adversity and offspring mental health problems can be ameliorated by promotive and protective factors during pregnancy, and (c) supporting resilience in pregnant women through translational prevention and intervention efforts. This section reviews each of these three areas.

Prenatal maternal stress and offspring adaptation to the postnatal environment

The links between prenatal maternal stress and fetal development are typically viewed through the lens of pathology. However, signals of maternal stress provide information to the fetus about the quality of the postnatal world that may have an adaptive benefit for survival in a given postnatal environment. The most well-documented example of this comes from nutrition. It is widely known that the prenatal period is a sensitive window when the fetus responds to nutritional deprivation with the development of a “thrifty phenotype” that promotes survival in an environment where food is scarce but is maladaptive and increases risk for metabolic disease when food is plentiful (Gluckman, Hanson & Pinal, Reference Yim, Glynn, Schetter, Hobel, Chicz-Demet and Sandman2005). These findings highlight the necessity of considering the larger context, including the postnatal environment, to understand the impact of prenatal stress and maternal mental health, elucidate their role in the developmental course, and identify appropriate interventions.

During pregnancy, biological stress signals, such as placental CRH, also transmit information to the fetus and shape the developmental course. The metamorphosis of the Western Spadefoot Toad illustrates the role stress hormones may play as a gestational signal that reflects the quality of the environment, affect development, and have implications for survival. This toad has a fascinating adaptive response to adversity (Denver, Reference Denver1997). When its pool of water desiccates rapidly, the tadpole adapts to this harsh environment by accelerating metamorphosis into a toad that is able to survive outside of water. However, a consequence of this accelerated developmental trajectory is that the toad is both smaller and less successful at foraging and reproducing as compared to a toad that had a more optimal environment allowing for a protracted developmental course. Stress hormones play a central role in this adaptive process. If CRH receptors are blocked, the tadpole's metamorphosis will not be accelerated in the context of a rapidly evaporating pool of water, and the tadpole will not survive.

The human fetus similarly incorporates signals from the maternal host environment into its developmental trajectory. The stress signal placental CRH is similarly associated with both shortened gestation and preterm birth in humans as well as accelerated maturation (Class et al., Reference Class, Buss, Davis, Gierczak, Pattillo, Chicz-DeMet and Sandman2008; Sandman et al., Reference Sandman, Glynn, Schetter, Wadhwa, Garite, Chicz-DeMet and Hobel2006; Swales et al., Reference Swales, Grande, Wing, Edelmann, Glynn, Sandman and Davis2019), and these alterations may have adaptive advantages for survival; for example, stressed fetuses tend to have greater lung maturity when born preterm (Dunkel Schetter, Reference Dunkel Schetter2009; Glynn et al., Reference Glynn, Dunkel Schetter, Hobel and Sandman2008). Like the toad, these adaptations are advantageous if the fetus is born preterm, but also may have long-term costs (Davis, Glynn, et al., Reference Davis, Glynn, Waffarn and Sandman2011; Stout, Espel, Sandman, Glynn, & Davis, Reference Stout, Espel, Sandman, Glynn and Davis2015).

Prenatal adaptations made by the offspring may further impact postnatal developmental trajectories. Studies have shown that placental CRH is linked to postnatal growth trajectories. For instance, elevated placental CRH predicts accelerated increases in BMI during the first postnatal year (Stout et al., Reference Stout, Espel, Sandman, Glynn and Davis2015). Prenatal fetal adaptations additionally may impact behavioral regulation, as elevated placental CRH in utero have been found to predict offspring's increased internalizing problems (Davis et al., Reference Davis, Glynn, Dunkel Schetter, Hobel, Chicz-De Met and Sandman2005; Howland et al., Reference Howland, Sandman, Glynn, Crippen and Davis2016) and may have persisting consequences for brain development during childhood (Curran, Sandman, Davis, Glynn, & Baram, Reference Curran, Sandman, Davis, Glynn and Baram2017; Sandman et al., Reference Sandman, Curran, Davis, Glynn, Head and Baram2018). Further, neuroimaging studies indicate that in utero exposure to adversity is associated with alterations in the functional architecture of the infant brain, most notably in limbic–prefrontal circuitry that may reflect accelerated maturation. In a study by Posner et al. (Reference Posner, Cha, Wang, Talati, Warner, Gerber and Weissman2016), 6-week old infants exposed to prenatal maternal depression demonstrated increased inverse (i.e., increased negative) resting state functional connectivity between the amygdala and bilateral dorsal prefrontal cortex and ventromedial prefrontal cortex. The authors interpret these data as consistent with the hypothesis of a more mature pattern. However, both increased and decreased connectivity have been observed in resting state and depending on the type of task that is used (Gee et al., Reference Gee, Gabard-Durnam, Flannery, Goff, Humphreys, Telzer and Tottenham2013). Future research with replication and longitudinal follow-up is needed to determine whether the observation that prenatal adversity is associated with resting state functional connectivity reflects accelerated maturation. However, these data are suggestive that early experiences shape developmental trajectories in ways that may be adaptive, but also increase risk for subsequent mental health problems (Tottenham, Reference Tottenham2020).

Moreover, as with nutrition, stress signals in the in-utero environment may set expectations for the postnatal world. The degree of concordance of maternal depression symptoms during pregnancy and postpartum predicted cognitive function during infancy. Specifically, the more consistent the pre- and postnatal periods, the better infants performed on the Bayley Scale of Mental Development (Sandman, Davis, & Glynn, Reference Sandman, Davis and Glynn2012).

Reframing our understanding of prenatal signals as information that shape the developmental course with potential adaptive benefits for the offspring highlights the importance of considering the broader context and the potential that prenatal stress may have benefits in certain contexts. There is, however, another implication for this adaptation framework that further highlights the need for preconception and prenatal prevention and intervention efforts for the mother in order to optimize benefits. The fetal programing literature provides robust evidence that the prenatal environment is incorporated into the offspring's developmental course and is associated with profound and long-lasting sequelae. Thus, preconception and prenatal efforts that aim to promote resilience, by either leveraging existing promotive and protective factors and resources, or implementing preventive interventions, are likely to have the greatest positive long-term benefit.

Promotive and protective factors that ameliorate negative outcomes following maternal adversity, mental health problems, and stress

It is critical to understand promotive and protective factors either prior to or during pregnancy that can promote maternal and fetal resilience and positive postnatal outcomes. Although much of the extant literature focuses on risk factors for maternal mental health problems and stress during pregnancy, studies find, for example, that a history of positive childhood experiences and better current social support during pregnancy are associated with better prenatal mental health and better child outcomes. For example, a mother's report of more positive relationships with her parental figures and the presence of more affection during childhood were associated with fewer prenatal depression symptoms (Chung, Mathew, Elo, Coyne, & Culhane, Reference Chung, Mathew, Elo, Coyne and Culhane2008). In another study, pregnant women's higher numbers of reported benevolent childhood experiences (BCEs) involving supportive relationships and a positive and predictable quality of life were associated with fewer mental health problems and lower exposure to adversity during pregnancy (Narayan et al., Reference Narayan, Rivera, Bernstein, Harris and Lieberman2018). These studies suggest that although less frequently studied, positive early-life experiences also likely have intergenerational benefits through the prenatal period. Although many of these studies rely on retrospective reports of positive childhood which may be impacted by current mental health and other factors, there is evidence for convergence between prospective and retrospective reports (e.g., Glynn et al., Reference Glynn, Stern, Howland, Risbrough, Baker, Nievergelt and Davis2019). Further, current depression symptoms are only modestly associated with positive memories from childhood (Narayan, Ippen, Harris, & Lieberman, Reference Narayan, Ippen, Harris and Lieberman2019). More research is needed to compare the relative strength of prospectively- versus retrospectively-assessed positive childhood experiences on wellbeing specifically in pregnant women.

In terms of proximal resources, social support during pregnancy is strongly associated with women's prenatal mental health (Dunkel Schetter, Sagrestano, Feldman, & Killingsworth, Reference Dunkel Schetter, Sagrestano, Feldman. and Killingsworth1996; Dunkel Schetter, Reference Dunkel Schetter2011; Sperlich & Seng, Reference Sperlich and Seng2008). Studies that examine both high-income and low-income women across a range of ethnic groups show that higher perceived effectiveness of social support from the baby's father and other counterparts, as well as greater availability of help in general, is associated with lower levels of anxiety and depression symptoms during pregnancy (Dunkel Schetter, Reference Dunkel Schetter2011; River, Narayan, Atzl, Rivera, & Lieberman, Reference River, Narayan, Atzl, Rivera and Lieberman2020; Séguin, Potvin, Denis, & Loiselle, Reference Séguin, Potvin, Denis and Loiselle1995). Furthermore, studies that have covaried for women's histories of childhood adversity and current stressful life events continue to find that the presence of high-quality social support is associated with benefits for women's prenatal mental health (Racine et al., Reference Racine, Zumwalt, McDonald, Tough and Madigan2019; Séguin et al., Reference Séguin, Potvin, Denis and Loiselle1995). Acknowledging the likely bidirectional nature of the association, in that women with better mental health may both experience and report better social relationships, it is important to note that high social support is one of the most robust correlates of better maternal mental health and more optimal birth outcomes.

The benefits of social support to pregnant women also extend to more positive infant outcomes. For instance, higher levels of perceived social support from the babies’ fathers predicted more positive postnatal Maternal×Infant interactions through lower levels of maternal prenatal depression symptoms. Higher levels of social support also predicted infants’ more effective cortisol reactivity following a stressor partially mediated by both lower levels of prenatal depression and more positive Mother×Infant interactions (Thomas, Letourneau, Bryce, Campbell, & Giesbrecht, Reference Thomas, Letourneau, Bryce, Campbell and Giesbrecht2017). Another study found that when levels of maternal depression symptoms were lower or levels of general maternal prenatal social support (not specifically from the father of the baby) were higher, the associations between infants’ negative temperament and their cortisol levels were attenuated, suggesting protective effects of both better prenatal mental health and greater social support (Luecken, MacKinnon, Jewell, Crnic, & Gonzales, Reference Luecken, MacKinnon, Jewell, Crnic and Gonzales2015). These studies together point to the potential of social support to help promote and buffer postnatal adaptation in the infant and the mother–infant relationship, in conjunction with the additional positive effect that higher social support likely also has on alleviating prenatal depression symptoms. Few studies have examined whether social support may help to ameliorate effects of maternal prenatal PTSD on postnatal adaptation, but this is a viable area of future inquiry.

An additional consideration is that the nuances of social support and its benefits may be complicated to measure during pregnancy, particularly for women with lifelong and cumulative risks. For instance, pregnant women who have been maltreated as children often confront painful decisions about whether and to what extent they may draw from support from previously abusive caregivers when caring for their new babies (Sperlich & Seng, Reference Sperlich and Seng2008). Relying less on social support from previously maltreating caregivers is associated with a reduction in the risk of childhood maltreatment when babies were born, even among women who continued to have elevated depression (Easterbrooks, Chaudhuri, Bartlett, & Copeman, Reference Easterbrooks, Chaudhuri, Bartlett and Copeman2011). Thus, in this case resilience may be enhanced by reducing contact with sources of childhood adversity. Furthermore, women's reports of the support they currently receive from their partner during pregnancy may be influenced by idealized views of the support they hope to receive when the baby is born. One study found that women actually had poorer mental health and higher levels of stress during pregnancy if they self-reported high levels of support from partners but were rated by trained coders to actually have low levels of support based on their open-ended descriptions of partners (River, Narayan, Atzl et al., Reference River, Narayan, Atzl, Rivera and Lieberman2019). These findings indicate that self-reports of social support, the most common strategy of assessment, are likely impacted by other factors including pregnancy related experiences and maternal mental health. Additional research is needed to assess pregnant women's social support from various counterparts using a variety of methodologies beyond self-report.

More research also is needed to identify broader promotive and protective factors that buffer against the intergenerational transmission of mental health problems and stress from mothers to babies. Given the enduring effects of childhood experiences, this may be particularly important in pregnant women with histories of childhood adversity. For instance, a recent review identified only 18 published studies on research that supported or promoted health, well-being, and resilience in pregnant women with childhood adversity, with fewer than a dozen of these specifically focused on factors that buffer against effects of maternal childhood adversity on prenatal mental health problems (Atzl, Grande, Davis, & Narayan, Reference Atzl, Grande, Davis and Narayan2019). This review found that social support was the most widely studied resource for pregnant women with childhood adversity; however, the total number of studies on social support were still surprisingly few. This dearth of research points to an underdeveloped literature on perinatal promotive and protective factors in contexts of adversity.

Translational efforts and interventions for prenatal mental health and stress

Targeted clinical efforts, such as preventive interventions, are needed to address and reduce pregnant women's mental health and stress. Prenatal care represents an opportunity to reach and to provide support and intervention for pregnant women. Although screening for perinatal depression and anxiety is now becoming the standard of care (American College of Obstetricians and Gynecologists (ACOG), 2018), routine prenatal screening is often not sufficient. Moreover, neither symptoms of prenatal PTSD nor exposure to childhood adversity are regularly screened prenatally.

Research shows that routine prenatal care may also be fraught with barriers, especially for women with high levels of mental health problems and stress, low-income women, and women from racial and ethnic minority groups (Narayan et al., Reference Narayan, Rivera, Bernstein, Castro, Gantt, Thomas and Lieberman2017; Sperlich & Seng, Reference Sperlich and Seng2008; River, Narayan, Galvan et al., Reference River, Narayan, Galvan, Rivera, Harris and Lieberman2019). Evidence suggests that only a minority of clinically depressed women (18%) (Marcus, Reference Marcus2009) seek treatment during the prenatal and postpartum periods. Even when women receive appropriate referrals for mental health treatment from their providers, depression and PTSD symptoms can continue to interfere with the ability to connect with and maintain adequate healthcare alliances and interpersonal support during pregnancy (Seng, Reference Seng2002). Another study showed that one third of pregnant women with clinical levels of depression and PTSD symptoms in their second or third trimester of pregnancy declined referrals for mental health services during pregnancy (Narayan et al., Reference Narayan, Rivera, Bernstein, Castro, Gantt, Thomas and Lieberman2017). An additional set of barriers pertain to childhood adversity. Many pregnant women with unresolved trauma histories and resulting untreated mental health problems report feeling pressure to suppress their own needs and focus on their babies during pregnancy (Narayan et al., Reference Narayan, Rivera, Bernstein, Castro, Gantt, Thomas and Lieberman2017; River, Narayan, Galvan et al., Reference River, Narayan, Galvan, Rivera, Harris and Lieberman2019; Sperlich & Seng, Reference Sperlich and Seng2008). Because current routine screening does not typically include assessment of childhood adversity, women with trauma histories may be even less recognized as needing support.

The prenatal period represents a key opportunity to reach such underserved, high-risk populations of women with more formalized and targeted translational efforts. Many women do have both increased motivation and increased contact with the medical system during the prenatal period (Sperlich & Seng, Reference Sperlich and Seng2008). We briefly review a sample of intervention efforts that are designed to address prenatal mental health problems and sources of adversity stemming from childhood trauma and lack of support within the romantic or co-parenting relationship.

One recent approach combines basic research with therapeutic assessment during pregnancy to represent a “foot-in-the-door” technique to connect women to services. A series of studies conducted with low-income and racially and ethnically diverse pregnant women in San Francisco and Denver revealed that pregnant women appreciate participating in focused clinical research study that assesses childhood adversity and mental health problems in conjunction with positive childhood experiences and ongoing support. This clinical research endeavor blended assessment of risks and resources to leverage existing protective factors and start a conversation about additional services and programs that may meet the needs of pregnant women. Pregnant women involved in these studies reported appreciating the opportunity to identify and process painful experiences of adversity that may be previously unrecognized sources of mental health problems and stress, and then having the opportunity to connect to more formalized, tailored services and preventive interventions during pregnancy, depending on their needs and other priorities (Narayan et al., Reference Narayan, Rivera, Bernstein, Castro, Gantt, Thomas and Lieberman2017, 2019).

The Care Project is a prenatal intervention that directly addresses barriers to mental health treatment and assesses benefits for mothers and their children (Davis et al., Reference Davis, Hankin, Swales and Hoffman2018). This project implements MomCare, a form of brief interpersonal psychotherapy (IPT) for depression during the prenatal period that is designed to meet the needs of low-income women from culturally diverse backgrounds and improve both maternal and infant outcomes. MomCare is a culturally-relevant, collaborative care intervention that provides brief IPT via approximately eight sessions after an initial engagement session (Grote et al., Reference Grote, Katon, Russo, Lohr, Curran, Galvin and Carson2015). MomCare is efficacious with socio-economically disadvantaged pregnant women of diverse cultural backgrounds; women randomized to MomCare showed significantly higher rates of depression remission and lower depressive symptom severity as compared to controls. These effects persisted through 18 months postpartum (effect sizes = .35 for severity of depressive symptoms and .36 for depression remission) (Grote et al., Reference Grote, Katon, Russo, Lohr, Curran, Galvin and Carson2015). Of note, MomCare is particularly beneficial for women with histories of adversity (Grote, Zuckoff, Swartz, Bledsoe, & Geibel, Reference Grote, Zuckoff, Swartz, Bledsoe and Geibel2007, Reference Grote, Katon, Russo, Lohr, Curran, Galvin and Carson2015). An important aspect of MomCare's success is that women participate in an initial engagement session to problem solve common barriers to treatment.

The goal of the Care Project specifically is to test whether reducing maternal depression affects child developmental outcomes, as the long-term benefits to offspring following prenatal interventions delivered to women remain unknown (Davis et al., Reference Davis, Hankin, Swales and Hoffman2018; Garcia et al., Reference Garcia, Valente, Lillehei, Grote, Hankin and Davis2019). In the Care Project, women with elevated depression symptoms are randomly assigned to receive either MomCare or the standard of care. Mothers are followed throughout the prenatal period and mother–infant dyads are assessed from birth until the infant is 18 months of age. In addition to assessing maternal trajectories of mental health and stress, infant brain development, cognitive function and emotional regulation are evaluated throughout the postpartum period. This project tests the hypothesis that maternal intervention during the prenatal period will exert benefits for both the mother and infant. The use of random assignment in this project addresses some of the limitations of correlational research. If reducing maternal depression during the prenatal period benefits infant brain development than this would provide support for the Fetal Programming Hypothesis and underscore the importance of beginning intervention prior to birth.

Perinatal Child–Parent Psychotherapy (CPP) and MotherWise are two additional evidence-based interventions during pregnancy that address maternal childhood adversity and relationship-based adversity with the father of the baby. Perinatal CPP aims to prevent the intergenerational transmission of adversity and mental health problems from mothers to children by helping women to process and recover from unresolved trauma before babies are born, as well as increase awareness of and attunement to the fetus, and strengthen positive attributions of infants (Lieberman et al., Reference Lieberman, Díaz and Van Horn2009; Narayan, Oliver Bucio, Rivera, & Lieberman, Reference Narayan, Oliver Bucio, Rivera and Lieberman2016). MotherWise, a relationship-based program, aims to strengthen communication skills and healthy conflict resolution strategies during pregnancy using the evidence-based Within My Reach curriculum (Rhoades, Mazzoni, & O'Reilly Treter, Reference Rhoades, Mazzoni and O'Reilly Treter2019). It also provides support for women to safely exit relationships that could be harmful to maternal and fetal wellbeing. MotherWise is multi-format and involves group-based workshops for pregnant women and couples, as well as individual case management, with the goal to improve birth and child outcomes, in addition to maternal wellbeing and relationship functioning (Rhoades et al., Reference Rhoades, Mazzoni and O'Reilly Treter2019). Together, all of the above intervention efforts aim to implement resources and foster resilience during the pregnancy period to promote long-term maternal, fetal, and relational wellbeing before babies are born. More translational prevention efforts that reduce mental health problems and stress dysregulation and are delivered during pregnancy or even prior to conception are needed to bolster resources and protective capacities in women before adversity occurs and mental health problems escalate.

Conclusions

There is growing awareness that maternal experiences of childhood and cumulative adversity may have intergenerational effects, making the prenatal period not only a window when the consequences of maternal adversity and resulting problems with mental health and stress physiology impact the fetus, but also a window of opportunity for resilience and intervention (Davis et al., Reference Davis, Hankin, Swales and Hoffman2018; Narayan et al., Reference Narayan, Ippen, Harris and Lieberman2019; Sperlich & Seng, Reference Sperlich and Seng2008; Yehuda & Meaney, Reference Yehuda and Meaney2018). The extant literature provides compelling evidence that the trajectory of fetal development is profoundly influenced by the intrauterine environment, including signals to the fetus that stem from maternal stress and mental health problems. However, these findings also provide support that the prenatal period is a window of opportunity to disrupt this intergenerational transmission of adversity and mental health problems from mothers to infants.

Several targeted areas of additional research are needed. Given the life span and intergenerational pathways linking maternal childhood and cumulative adversity, mental health problems before and during pregnancy, disruptions in maternal–fetal stress physiology, and negative neonatal and infant outcomes, more research needs to utilize study designs that account for as many of these variables as possible. Such studies could leverage intergenerational designs not only to better understand how the pregnancy period is a unique time of risk, but also to harness resilience processes that may promote or buffer adaptation across generations, particularly in families with maternal childhood adversity. There is a significant gap in research that examines prenatal protective factors that buffer against the effects of maternal childhood adversity on alterations in maternal–fetal stress physiology.

Research is needed to clarify whether effects of childhood adversity on maternal mental health and stress physiology during pregnancy depend on whether the adversity was measured retrospectively or prospectively. Recent research has shown that childhood adversity assessed with retrospective measurement is valid and shows similar associations to outcomes than prospective assessments (e.g., Glynn et al., Reference Glynn, Stern, Howland, Risbrough, Baker, Nievergelt and Davis2019), although associations between retrospectively reported adversity and outcomes may be impacted by contemporaneous factors (e.g., mental state, trait negativity, ongoing stress; Reuben et al., Reference Reuben, Moffitt, Caspi, Belsky, Harrington, Schroeder and Danese2016). However, prospective data on childhood adversity, such as child welfare records of documented maltreatment, also have disadvantages; official records may miss cases that either were not reported at all or did not rise to the level of attention needed for substantiation. Thus, both retrospective and prospective data on childhood adversity have advantages and disadvantages. Their relative predictive strength for various aspects of prenatal maternal and fetal wellbeing is an important area for future research.

Finally, PTSD continues to be an understudied mental health problem in pregnant women. More research should be dedicated to antecedents of maternal prenatal PTSD, such as the role of social support and pre-conception stressors, and the interaction between maternal adversity and PTSD before and during pregnancy on maternal–fetal stress physiology. PTSD symptoms, as well as childhood adversity, should also be routinely screened in all pregnant women. Stronger and more focused empirical and translational efforts to understand pathways of intergenerational risk and resilience through the pregnancy period will extend and enhance the burgeoning literature base and continue to promote optimal health and wellbeing in mothers and children across development and over generations.

Funding Statement

This research was supported by the National Institutes of Health (P50 MH096889 and R01 MH109662) to EPD and the Society for Research in Child Development Small Grants Program for Early Career Scholars to AJN.

Conflicts of Interest

None.

References

American College of Obstetricians and Gynecologists (ACOG). (2018). Screening for perinatal depression. https://www.acog.org/clinical/clinical-guidance/committee-opinion/articles/2018/11/screening-for-perinatal-depressionGoogle Scholar
Atzl, V. M., Grande, L. A., Davis, E. P., & Narayan, A. J. (2019). Perinatal promotive and protective factors for women with histories of childhood abuse and neglect. Child Abuse & Neglect, 91, 6377. doi:10.1016/j.chiabu.2019.02.008CrossRefGoogle ScholarPubMed
Atzl, V. M., Narayan, A. J., Rivera, L. M., & Lieberman, A. F. (2019). Adverse childhood experiences and prenatal mental health: Type of ACEs and age of maltreatment onset. Journal of Family Psychology, 33, 304314. doi:10.1037/fam0000510CrossRefGoogle ScholarPubMed
Barker, D. J. (1998). In utero programming of chronic disease. Clinical Science, 95, 115128. doi:10.1042/cs0950115CrossRefGoogle ScholarPubMed
Barker, D. J. (2002). Fetal programming of coronary heart disease. Trends in Endocrinology and Metabolism, 13, 364368. doi:10.1016/S1043-2760(02)00689-6CrossRefGoogle ScholarPubMed
Barker, D. J., Eriksson, J. G., Forsen, T., & Osmond, C. (2002). Fetal origins of adult disease: Strength of effects and biological basis. International Journal of Epidemiology, 31, 12351239. doi:10.1093/ije/31.6.1235CrossRefGoogle ScholarPubMed
Barker, E. D., Jaffee, S. R., Uher, R., & Maughan, B. (2011). The contribution of prenatal and postnatal maternal anxiety and depression to child maladjustment. Depression and Anxiety, 28, 696702. doi:10.1002/da.20856CrossRefGoogle ScholarPubMed
Blair, M. M., Glynn, L. M., Sandman, C. A., & Davis, E. P. (2011). Prenatal maternal anxiety and early childhood temperament. Stress, 14, 644651. doi:10.3109/10253890.2011.594121CrossRefGoogle ScholarPubMed
Bourgeois, J. P. (1997). Synaptogenesis, heterochrony and epigenesis in the mammalian neocortex. Acta Paediatrica, 422, 2733. doi:10.1111/j.1651-2227.1997.tb18340.xCrossRefGoogle ScholarPubMed
Bourgeois, J. P., Goldman-Rakic, P. S., & Rakic, P. (1994). Synaptogenesis in the prefrontal cortex of rhesus monkeys. Cerebral Cortex (New York, N.Y.: 1991), 4, 7896. https://doi.org/10.1093/cercor/4.1.78CrossRefGoogle ScholarPubMed
Bowers, M. E., & Yehuda, R. (2016). Intergenerational transmission of stress in humans. Neuropsychopharmacology, 41, 232244. doi:10.1038/npp.2015.247CrossRefGoogle ScholarPubMed
Bowers, M. E., & Yehuda, R. (2020). Intergenerational transmission of stress vulnerability and resilience. In Chen, A. (Ed.), Stress resilience (pp. 257267). London, England: Academic Press.10.1016/B978-0-12-813983-7.00017-3CrossRefGoogle Scholar
Brand, S. R., Engel, S. M., Canfield, R. L., & Yehuda, R. (2006). The effect of maternal PTSD following in utero trauma exposure on behavior and temperament in the 9-month-old infant. Annals of the New York Academy of Sciences, 1071, 454458. doi:10.1196/annals.1364.041CrossRefGoogle ScholarPubMed
Burton, G. J., Hempstock, J., & Jauniaux, E. (2001). Nutrition of the human fetus during the first trimester--a review. Placenta, 22, S70S77. doi:10.1053/plac.2001.0639CrossRefGoogle Scholar
Buss, C., Davis, E. P., Class, Q. A., Gierczak, M., Pattillo, C., Glynn, L. M., & Sandman, C. A. (2009). Maturation of the human fetal startle response: Evidence for sex-specific maturation of the human fetus. Early Human Development, 85, 633638. doi:10.1016/j.earlhumdev.2009.08.001CrossRefGoogle ScholarPubMed
Buss, C., Davis, E. P., Shahbaba, B., Pruessner, J. C., Head, K., & Sandman, C. A. (2012). Maternal cortisol over the course of pregnancy and subsequent child amygdala and hippocampus volumes and affective problems. Proceedings of the National Academy of Sciences of the United States of America, 109, E1312E1319. doi:10.1073/pnas.1201295109Google ScholarPubMed
Buss, C., Entringer, S., Moog, N. K., Toepfer, P., Fair, D. A., Simhan, H. N., … Wadhwa, P. D. (2017). Intergenerational transmission of maternal childhood maltreatment exposure: Implications for fetal Brain development. Journal of the American Academy of Child and Adolescent Psychiatry, 56, 373382. doi:10.1016/j.jaac.2017.03.001CrossRefGoogle ScholarPubMed
Buss, C., Entringer, S., Reyes, J. F., Chicz-DeMet, A., Sandman, C. A., Waffarn, F., & Wadhwa, P. D. (2009). The maternal cortisol awakening response in human pregnancy is associated with the length of gestation. American Journal of Obstetrics and Gynecologyl, 201, 398.e1398.e8. doi:10.1016/j.ajog.2009.06.063CrossRefGoogle ScholarPubMed
Cai, D., Zhu, Z., Sun, H., Qi, Y., Xing, L., Zhao, X., … Li, H. (2017). Maternal PTSD following exposure to the Wenchuan Earthquake is associated with impaired mental development of children. PLoS One, 12, e0168747. doi:10.1371/journal.pone.0168747CrossRefGoogle Scholar
Capron, L. E., Glover, V., Pearson, R. M., Evans, J., O'Connor, T. G., Stein, A., … Ramchandani, P. G. (2015). Associations of maternal and paternal antenatal mood with offspring anxiety disorder at age 18 years. Journal of Affective Disorders, 187, 2026. doi:10.1016/j.jad.2015.08.012CrossRefGoogle ScholarPubMed
Center for Disease Control and Prevention (CDC). (2019a). Adverse childhood experiences (ACEs). https://www.cdc.gov/vitalsigns/aces/index.htmlGoogle Scholar
Center for Disease Control and Prevention (CDC). (2019b). Depression among women. https://www.cdc.gov/reproductivehealth/depression/index.htmGoogle Scholar
Chambliss, L. R. (2008). Intimate partner violence and its implication for pregnancy. Clinical Obstetrics & Gynecology, 51, 385397. doi:10.1097/GRF.0b013e31816f29ceCrossRefGoogle ScholarPubMed
Choi, K. W., & Sikkema, K. J. (2016). Childhood maltreatment and perinatal mood and anxiety disorders: A systematic review. Trauma, Violence, and Abuse, 17, 427453. doi:10.1177/1524838015584369CrossRefGoogle ScholarPubMed
Chung, E. K., Mathew, L., Elo, I. T., Coyne, J. C., & Culhane, J. F. (2008). Depressive symptoms in disadvantaged women receiving prenatal care: The influence of adverse and positive childhood experiences. Ambulatory Pediatrics, 8, 109116. doi:10.1016/j.ambp.2007.12.003CrossRefGoogle ScholarPubMed
Class, Q. A., Buss, C., Davis, E. P., Gierczak, M., Pattillo, C., Chicz-DeMet, A., & Sandman, C. A. (2008). Low levels of corticotropin-releasing hormone during early pregnancy are associated with precocious maturation of the human fetus. Developmental Neuroscience, 30, 419426. doi:10.1159/000191213CrossRefGoogle ScholarPubMed
Clemens, C. C., Castro, V. M., Blumenthal, S. R., Rosenfield, H. R., Murphy, S. N., Fava, M., & Robinson, E. B. (2015). Prenatal antidepressant exposure is associated with risk for attention-deficit hyperactivity disorder but not autism spectrum disorder in a large health system. Molecular Psychiatry, 20, 727734. doi:10.1038/mp.2014.90CrossRefGoogle Scholar
Cook, N., Ayers, S., & Horsch, A. (2018). Maternal posttraumatic stress disorder during the perinatal period and child outcomes: A systematic review. Journal of Affective Disorders, 225, 1831. doi:10.1016/j.jad.2017.07.045CrossRefGoogle ScholarPubMed
Curran, M. M., Sandman, C. A., Davis, E. P., Glynn, L. M., & Baram, T. Z. (2017). Abnormal dendritic maturation of developing cortical neurons exposed to corticotropin releasing hormone (CRH): Insights into effects of prenatal adversity? PLoS One, 12, e0180311. doi:10.1371/journal.pone.0180311CrossRefGoogle ScholarPubMed
Davis, E. P., Buss, C., Muftuler, L. T., Head, K., Hasso, A., Wing, D. A., … Sandman, C. A. (2011). Children's brain development benefits from longer gestation. Frontiers in Psychology, 2, 1. doi:10.3389/fpsyg.2011.00001CrossRefGoogle ScholarPubMed
Davis, E. P., Glynn, L. M., Dunkel Schetter, C., Hobel, C., Chicz-De Met, A., & Sandman, C. A. (2005). Maternal plasma corticotropin-releasing hormone levels during pregnancy are associated with infant temperament. Developmental Neuroscience, 27, 299305. doi:10.1159/000086709CrossRefGoogle Scholar
Davis, E. P., Glynn, L. M., Schetter, C. D., Hobel, C., Chicz-Demet, A., & Sandman, C. A. (2007). Prenatal exposure to maternal depression and cortisol influences infant temperament. Journal of the American Academy of Child and Adolescent Psychiatry, 46, 737746. doi:10.1097/chi.0b013e318047b775CrossRefGoogle ScholarPubMed
Davis, E. P., Glynn, L. M., Waffarn, F., & Sandman, C. A. (2011). Prenatal maternal stress programs infant stress regulation. Journal of Child Psychology and Psychiatry, 52, 119129. doi:10.1111/j.1469-7610.2010.02314.xCrossRefGoogle ScholarPubMed
Davis, E. P., Hankin, B. L., Glynn, L. M., Head, K., Kim, D. J., & Sandman, C. A. (2019). Prenatal maternal stress, child cortical thickness, and adolescent depressive symptoms. Child Development, 91, e432e450. doi:10.1111/cdev.13252Google ScholarPubMed
Davis, E. P., Hankin, B. L., Swales, D. A., & Hoffman, M. C. (2018). An experimental test of the fetal programming hypothesis: Can we reduce child ontogenetic vulnerability to psychopathology by decreasing maternal depression? Development and Psychopathology, 30, 787806. doi:10.1017/s0954579418000470CrossRefGoogle ScholarPubMed
Davis, E. P., Head, K., Buss, C., & Sandman, C. A. (2017). Prenatal maternal cortisol concentrations predict neurodevelopment in middle childhood. Psychoneuroendocrinology, 75, 5663. doi:10.1016/j.psyneuen.2016.10.005CrossRefGoogle ScholarPubMed
Davis, E. P., & Pfaff, D. (2014). Sexually dimorphic responses to early adversity: Implications for affective problems and autism spectrum disorder. Psychoneuroendocrinology, 49, 1125. doi:10.1016/j.psyneuen.2014.06.014CrossRefGoogle ScholarPubMed
Davis, E. P., & Sandman, C. A. (2010). The timing of prenatal exposure to maternal cortisol and psychosocial stress is associated with human infant cognitive development. Child Development, 81, 131148. doi:10.1111/j.1467-8624.2009.01385.xCrossRefGoogle ScholarPubMed
Davis, E. P., & Sandman, C. A. (2012). Prenatal psychobiological predictors of anxiety risk in preadolescent children. Psychoneuroendocrinology, 37, 12241233. doi:10.1016/j.psyneuen.2011.12.016CrossRefGoogle ScholarPubMed
Davis, E. P., Snidman, N., Wadhwa, P. D., Dunkel Schetter, C., Glynn, L., & Sandman, C. A. (2004). Prenatal maternal anxiety and depression predict negative behavioral reactivity in infancy. Infancy, 6, 319331. doi:10.1207/s15327078in0603_1CrossRefGoogle Scholar
Denver, R. J. (1997). Environmental stress as a developmental cue: Corticotropin-releasing hormone is a proximate mediator of adaptive phenotypic plasticity in amphibian metamorphosis. Hormones and Behavior, 31, 169179. doi: 10.1006/hbeh.1997.1383CrossRefGoogle ScholarPubMed
de Weerth, C. (2018). Prenatal stress and the development of psychopathology: Lifestyle behaviors as a fundamental part of the puzzle. Development and Psychopathology, 30, 11291144. doi:10.1017/s0954579418000494CrossRefGoogle ScholarPubMed
de Weerth, C., & Buitelaar, J. K. (2005). Physiological stress reactivity in human pregnancy--a review. Neuroscience & Biobehavioral Reviews, 29, 295312. doi:10.1016/j.neubiorev.2004.10.005CrossRefGoogle ScholarPubMed
Dunkel Schetter, C. (2009). Stress processes in pregnancy and preterm birth. Current Directions in Psychological Science, 18, 204209.Google Scholar
Dunkel Schetter, C. (2011). Psychological science on pregnancy: Stress processes, biopsychosocial models, and emerging research issues. Annual Review of Psychology, 62, 531558. doi:10.1146/annurev.psych.031809.130727CrossRefGoogle ScholarPubMed
Dunkel Schetter, C., Sagrestano, L. M., Feldman., , & Killingsworth, C. (1996). Social support and pregnancy. In Handbook of Social Support and the Family (pp. 375412). Boston, MA: Springer.10.1007/978-1-4899-1388-3_16CrossRefGoogle Scholar
Dunkel Schetter, C., & Tanner, L. (2012). Anxiety, depression and stress in pregnancy: Implications for mothers, children, research, and practice. Current Opinion in Psychiatry, 25, 141148. doi:10.1097/YCO.0b013e3283503680CrossRefGoogle Scholar
Easterbrooks, M. A., Chaudhuri, J. H., Bartlett, J. D., & Copeman, A. (2011). Resilience in parenting among young mothers: Family and ecological risks and opportunities. Children and Youth Services Review, 33, 4250. doi:10.1016/j.childyouth.2010.08.010CrossRefGoogle Scholar
El Marroun, H., White, T. J., Fernandez, G., Jaddoe, V. W. V., Verhulst, F. C., Stricker, B. H., & Tiemeier, H. (2017). Prenatal exposure to selective serotonin reuptake inhibitors and non-verbal cognitive functioning in childhood. Journal of Psychopharmacology, 31, 346355. doi:10.1177/0269881116665335CrossRefGoogle ScholarPubMed
Evans, L. M., Myers, M. M., & Monk, C. (2008). Pregnant women's cortisol is elevated with anxiety and depression—but only when comorbid. Archives of Women's Mental Health, 11, 239. doi:10.1007/s00737-008-0019-4CrossRefGoogle ScholarPubMed
Fahrbach, S. E., & Pfaff, D. W. (1986). Effect of preoptic region implants of dilute estradiol on the maternal behavior of ovariectomized, nulliparous rats. Hormones and Behavior, 20, 354363. doi:10.1016/0018-506x(86)90043-7CrossRefGoogle ScholarPubMed
Felitti, V. J., Anda, R. F., Nordenberg, D., Williamson, D. F., Spitz, A. M., Edwards, V., … Marks, J. S. (1998). Relationship of childhood abuse and household dysfunction to many of the leading causes of death in adults. The Adverse Childhood Experiences (ACE) Study. American Journal of Preventive Medicine, 14, 245258. doi: 10.1016/j.amepre.2019.04.001CrossRefGoogle ScholarPubMed
Flanagan, J. C., Gordon, K. C., Moore, T. M., & Stuart, G. L. (2015). Women's stress, depression, and relationship adjustment profiles as they relate to intimate partner violence and mental health during pregnancy and postpartum. Psychology of Violence, 5, 6673. doi:10.1037/a0036895CrossRefGoogle ScholarPubMed
Galbally, M., van Rossum, E. F. C., Watson, S. J., de Kloet, E. R., & Lewis, A. J. (2019). Trans-generational stress regulation: Mother-infant cortisol and maternal mental health across the perinatal period. Psychoneuroendocrinology, 109, 104374. doi:10.1016/j.psyneuen.2019.104374CrossRefGoogle ScholarPubMed
Garcia, S., Valente, E., Lillehei, N., Grote, N., Hankin, B. L., & Davis, E. P. (2019). Does brief psychotherapy with distressed pregnant women benefit both mother and baby? Zero to Three, 39, 2332.Google Scholar
Gee, D. G., Gabard-Durnam, L. J., Flannery, J., Goff, B., Humphreys, K. L., Telzer, E., … Tottenham, N. (2013). Early developmental emergence of human amygdala-prefrontal connectivity after maternal deprivation. Proceedings of the National Academy of Sciences of the United States of America, 110, 1563815643. doi:10.1073/pnas.1307893110CrossRefGoogle ScholarPubMed
Gilmore, J. H., Knickmeyer, R. C., & Gao, W. (2018). Imaging structural and functional brain development in early childhood. Nature Reviews Neuroscience, 19, 123137. https://doi.org/10.1038/nrn.2018.1CrossRefGoogle ScholarPubMed
Gluckman, P. D., & Hanson, M. A. (2004). Living with the past: Evolution, development, and patterns of disease. Science, 305, 17331736. doi:10.1126/science.1095292CrossRefGoogle ScholarPubMed
Gluckman, P. D., Hanson, M. A., & Pinal, C. (2005). The developmental origins of adult disease. Maternal & Child Nutrition, 1(3), 130141.10.1111/j.1740-8709.2005.00020.xCrossRefGoogle ScholarPubMed
Glynn, L. M. (2010). Giving birth to a new brain: Hormone exposures of pregnancy influence human memory. Psychoneuroendocrinology, 35, 11481155. doi:10.1016/j.psyneuen.2010.01.015CrossRefGoogle ScholarPubMed
Glynn, L. M. (2012). Increasing parity is associated with cumulative effects on memory. Journal of Women's Health, 21, 10381045. doi:10.1089/jwh.2011.3206CrossRefGoogle ScholarPubMed
Glynn, L. M., Davis, E. P., & Sandman, C. A. (2013). New insights into the role of perinatal HPA-axis dysregulation in postpartum depression. Neuropeptides, 47, 363370. doi:10.1016/j.npep.2013.10.007CrossRefGoogle ScholarPubMed
Glynn, L. M., Davis, E. P., Sandman, C. A., & Goldberg, W. A. (2016). Gestational hormone profiles predict human maternal behavior at 1-year postpartum. Hormones and Behavior, 85, 1925. doi:10.1016/j.yhbeh.2016.07.002CrossRefGoogle ScholarPubMed
Glynn, L. M., Dunkel Schetter, C., Hobel, C., & Sandman, C. A. (2008). Pattern of perceived stress and anxiety in pregnancy predict preterm birth. Health Psychology, 27, 4251. doi:10.1037/0278-6133.27.1.43CrossRefGoogle Scholar
Glynn, L. M., Howland, M. A., Sandman, C. A., Davis, E. P., Phelan, M., & Baram, T. Z., & Stern, H. Z. (2018). Prenatal maternal mood patterns predict child temperament and adolescent mental health. Journal of Affective Disorders, 228, 8390.10.1016/j.jad.2017.11.065CrossRefGoogle ScholarPubMed
Glynn, L. M., & Sandman, C. A. (2014). Evaluation of the association between placental corticotrophin-releasing hormone and postpartum depressive symptoms. Psychosomatic Medicine, 76, 355362. doi:10.1097/psy.0000000000000066CrossRefGoogle ScholarPubMed
Glynn, L. M., Schetter, C. D., Wadhwa, P. D., & Sandman, C. A. (2004). Pregnancy affects appraisal of negative life events. Journal of Psychosomatic Research, 56, 4752. doi:10.1016/S0022-3999(03)00133-8CrossRefGoogle ScholarPubMed
Glynn, L. M., Stern, H. S., Howland, M. A., Risbrough, V. B., Baker, D. G., Nievergelt, C. M., … Davis, E. P. (2019). Measuring novel antecedents of mental illness: The questionnaire of unpredictability in childhood. Neuropsychopharmacology, 44, 876882. doi:10.1038/s41386-018-0280-9CrossRefGoogle ScholarPubMed
Glynn, L. M., Wadhwa, P. D., Dunkel Schetter, C., & Sandman, C. A. (2001). When stress happens matters: The effects of earthquake timing on stress responsivity in pregnancy. American Journal of Obstetrics and Gynecology, 184, 637642. doi:10.1067/mob.2001.111066CrossRefGoogle ScholarPubMed
Godfrey, K. M., & Barker, D. J. (2001). Fetal programming and adult health. Public Health Nutrition, 4, 611624. doi:10.1079/phn2001145CrossRefGoogle ScholarPubMed
Goland, R. S. (1988). Biologically active corticotropin releasing hormone in maternal and fetal plasma during pregnancy. American Journal of Obstetrics and Gynecology, 159, 884–490. doi:10.1016/S0002-9378(88)80162-5CrossRefGoogle ScholarPubMed
Grigoriadis, S., VonderPorten, E. H., Mamisashvili, L., Tomlinson, G., Dennis, C. L., Koren, G., … Ross, L. E. (2013). The impact of maternal depression during pregnancy on perinatal outcomes: A systematic review and meta-analysis. Journal of Clinical Psychiatry, 74, e321e341. doi:10.4088/JCP.12r07968CrossRefGoogle ScholarPubMed
Grote, N. K., Bridge, J. A., Gavin, A. R., Melville, J. L., Iyengar, S., & Katon, W. J. (2010). A meta-analysis of depression during pregnancy and the risk of preterm birth, low birth weight, and intrauterine growth restriction. Archives of General Psychiatry, 67, 10121024. doi:10.1001/archgenpsychiatry.2010.111CrossRefGoogle ScholarPubMed
Grote, N. K., Katon, W. J., Russo, J. E., Lohr, M. J., Curran, M., Galvin, E., & Carson, K. (2015). Collaborative care for perinatal depression in socioeconomically disadvantaged women: A randomized trial. Depression and Anxiety, 32, 821834. doi:10.1002/da.22405CrossRefGoogle ScholarPubMed
Grote, N. K., Zuckoff, A., Swartz, H., Bledsoe, S. E., & Geibel, S. (2007). Engaging women who are depressed and economically disadvantaged in mental health treatment. Social Work, 52, 295308. doi:10.1093/sw/52.4.295CrossRefGoogle ScholarPubMed
Gunnar, M., & Quevedo, K. (2007). The neurobiology of stress and development. Annual Review of Psychology, 58, 145173. https://doi.org/10.1146/annurev.psych.58.110405.085605CrossRefGoogle ScholarPubMed
Harris-Britt, A., Martin, S. L., Li, Y., Casanueva, C., & Kupper, L. L. (2004). Posttraumatic stress disorder and associated functional impairments during pregnancy: Some consequences of violence against women. Journal of Clinical Psychology in Medical Settings, 11, 253264. doi:10.1023/B:JOCS.0000045345.72671.5eCrossRefGoogle Scholar
Hentges, R. F., Graham, S. A., Plamondon, A., Tough, S., & Madigan, S. (2019). A developmental cascade from prenatal stress to child internalizing and externalizing problems. Journal of Pediatric Psychology, 44, 10571067. doi:10.1093/jpepsy/jsz044CrossRefGoogle ScholarPubMed
Howland, M. A., Sandman, C. A., & Glynn, L. M. (2017). Developmental origins of the human hypothalamic-pituitary-adrenal axis. Expert Review of Endocrinology & Metabolism, 12, 321339. doi:10.1080/17446651.2017.1356222CrossRefGoogle ScholarPubMed
Howland, M. A., Sandman, C. A., Glynn, L. M., Crippen, C., & Davis, E. P. (2016). Fetal exposure to placental corticotropin-releasing hormone is associated with child self-reported internalizing symptoms. Psychoneuroendocrinology, 67, 1017. doi:10.1016/j.psyneuen.2016.01.023CrossRefGoogle ScholarPubMed
Huot, R., Brennan, P., Stowe, Z., Plotsky, P., & Walker, E. (2004). Negative affect in offspring of depressed mothers is predicted by infant cortisol levels at 6 months and maternal depression during pregnancy, but not postpartum. Annals of the New York Academy of Sciences, 1032, 234236. doi:10.1196/annals.1314.028CrossRefGoogle Scholar
Huth-Bocks, A. C., Krause, K., Ahlfs-Dunn, S., Gallagher, E., & Scott, S. (2013). Relational trauma and posttraumatic stress symptoms among pregnant women. Psychodynamic Psychiatry, 41, 277301. doi:10.1521/pdps.2013.41.2.277CrossRefGoogle ScholarPubMed
Jasinski, J. L. (2004). Pregnancy and domestic violence: A review of the literature. Trauma, Violence, & Abuse, 5, 4764. doi:10.1177/1524838003259322CrossRefGoogle ScholarPubMed
Keyser-Marcus, L., Stafisso-Sandoz, G., Gerecke, K., Jasnow, A., Nightingale, L., Lambert, K. G., … Kinsley, C. H. (2001). Alterations of medial preoptic area neurons following pregnancy and pregnancy-like steroidal treatment in the rat. Brain Research Bulletin, 55, 737745. doi:10.1016/s0361-9230(01)00554-8CrossRefGoogle ScholarPubMed
Kim, D. J., Davis, E. P., Sandman, C. A., Sporns, O., O'Donnell, B. F., Buss, C., & Hetrick, W. P. (2014). Longer gestation is associated with more efficient brain networks in preadolescent children. NeuroImage, 100, 619627. doi:10.1016/j.neuroimage.2014.06.048CrossRefGoogle ScholarPubMed
Kim, D. J., Davis, E. P., Sandman, C. A., Sporns, O., O'Donnell, B. F., Buss, C., & Hetrick, W. P. (2017). Prenatal maternal cortisol has sex-specific associations with child brain network properties. Cerebral Cortex, 27, 52305241. doi:10.1093/cercor/bhw303Google ScholarPubMed
King, S., & Laplante, D. P. (2005). The effects of prenatal maternal stress on children's cognitive development: Project ice storm. Stress, 8, 3545. doi:10.1080/10253890500108391CrossRefGoogle ScholarPubMed
King, B. R., Nicholson, R. C., & Smith, R. (2001). Placental corticotrophin-releasing hormone, local effects and fetomaternal endocrinology. Stress, 4, 219233. doi:10.3109/10253890109014747CrossRefGoogle ScholarPubMed
Korhonen, M., Luoma, I., Salmelin, R., & Tamminen, T. (2012). A longitudinal study of maternal prenatal, postnatal and concurrent depressive symptoms and adolescent well-being. Journal of Affective Disorders, 136, 680692. doi:10.1016/j.jad.2011.10.007CrossRefGoogle ScholarPubMed
Kostović, I., Judas, M., Rados, M., & Hrabac, P. (2002). Laminar organization of the human fetal cerebrum revealed by histochemical markers and magnetic resonance imaging. Cerebral Cortex (New York, N.Y.: 1991), 12, 536544. https://doi.org/10.1093/cercor/12.5.536CrossRefGoogle ScholarPubMed
Letourneau, N., Dewey, D., Kaplan, B. J., Ntanda, H., Novick, J., Thomas, J. C., … Giesbrecht, G. F. (2019). Intergenerational transmission of adverse childhood experiences via maternal depression and anxiety and moderation by child sex. Journal of Developmental Origins of Health and Disease, 10, 8899. doi:10.1017/s2040174418000648CrossRefGoogle ScholarPubMed
Lieberman, A. F., Díaz, M. A., & Van Horn, P. (2009). Safer beginnings: Perinatal child-parent psychotherapy for newborns and mothers exposed to domestic violence. Zero to Three, 29, 1722.Google Scholar
Luecken, L. J., MacKinnon, D. P., Jewell, S. L., Crnic, K. A., & Gonzales, N. A. (2015). Effects of prenatal factors and temperament on infant cortisol regulation in low-income Mexican American families. Developmental Psychobiology, 57, 961973. doi:10.1002/dev.21328CrossRefGoogle ScholarPubMed
Madigan, S., Oatley, H., Racine, N., Fearon, R. M. P., Schumacher, L., Akbari, E., … Tarabulsy, G. M. (2018). A meta-analysis of maternal prenatal depression and anxiety on child socioemotional development. Journal of the American Academy of Child and Adolescent Psychiatry, 57, 645657.e648. doi:10.1016/j.jaac.2018.06.012CrossRefGoogle ScholarPubMed
Marcus, S. M. (2009). Depression during pregnancy: Rates, risks and consequences – motherisk update 2008. Canadian Journal of Clinical Pharmacology, 16, 1522.Google ScholarPubMed
Mastorakos, G., & Ilias, I. (2003). Maternal and fetal hypothalamic–pituitary–adrenal axes during pregnancy and postpartum. Annals of the New York Academy of Science, 997, 136149. doi:10.1196/annals.1290.016CrossRefGoogle ScholarPubMed
McDonnell, C. G., & Valentino, K. (2016). Intergenerational effects of childhood trauma: Evaluating pathways among maternal ACEs, perinatal depressive symptoms, and infant outcomes. Child Maltreatment, 21, 317326. doi:10.1177/1077559516659556CrossRefGoogle ScholarPubMed
Moog, N. K., Entringer, S., Rasmussen, J. M., Styner, M., Gilmore, J. H., Kathmann, N., … Buss, C. (2018). Intergenerational effect of maternal exposure to childhood maltreatment on newborn brain anatomy. Biological Psychiatry, 83, 120127. doi:10.1016/j.biopsych.2017.07.009CrossRefGoogle ScholarPubMed
Moon, C. M., & Fifer, W. P. (2000). Evidence of transnatal auditory learning. Journal of Perinatology, 20, S37S44. doi:10.1038/sj.jp.7200448CrossRefGoogle ScholarPubMed
Narayan, A. J., Atzl, V. M., Merrick, J. S., River, L. M., & Peña, R. (2019). Therapeutic perinatal research with low-income families: Leveraging benevolent childhood experiences (BCEs) and fathers’ perspectives to promote resilience. Zero to Three, 39, 4353.Google Scholar
Narayan, A. J., Hagan, M. J., Cohodes, E., Rivera, L. M., & Lieberman, A. F. (2016). Early childhood victimization and physical intimate partner violence during pregnancy: A developmental and person-oriented approach. Journal of Interpersonal Violence, 3, 326.Google Scholar
Narayan, A. J., Ippen, C. G., Harris, W. W., & Lieberman, A. F. (2019). Protective factors that buffer against the intergenerational transmission of trauma from mothers to young children: A replication study of angels in the nursery. Development and Psychopathology, 31, 173187. doi:10.1017/S0954579418001530CrossRefGoogle ScholarPubMed
Narayan, A. J., Oliver Bucio, G., Rivera, L. M., & Lieberman, A. F. (2016). Making sense of the past creates space for the baby: Perinatal child-parent psychotherapy for pregnant women with childhood trauma. Zero to Three, 36, 2228.Google Scholar
Narayan, A. J., Rivera, L. M., Bernstein, R. E., Castro, G., Gantt, T., Thomas, M., … Lieberman, A. F. (2017). Between pregnancy and motherhood: Identifying unmet mental health needs in pregnant women with lifetime adversity. Zero to Three, 37, 413.Google Scholar
Narayan, A. J., Rivera, L. M., Bernstein, R. E., Harris, W. W., & Lieberman, A. F. (2018). Positive childhood experiences predict less psychopathology and stress in pregnant women with childhood adversity: A pilot study of the benevolent childhood experiences (BCEs) scale. Child Abuse & Neglect, 78, 1930. doi:10.1016/j.chiabu.2017.09.022CrossRefGoogle ScholarPubMed
Noroña, A., Doom, J., Davis, E. P., & Gunnar, M. R. (2020). The effects of stress on early brain and behavioral development. In Rubenstein, J. L. R., & Rakic, P. (Eds.), Comprehensive developmental neuroscience: Neural circuit development and function in the healthy and diseased brain. Amsterdam, Netherlands: Academic Press.Google Scholar
Numan, M. (2006). Hypothalamic neural circuits regulating maternal responsiveness toward infants. Behavioral and Cognitive Neuroscience Reviews, 5, 163190. doi: 10.1177/1534582306288790CrossRefGoogle ScholarPubMed
Numan, M., Rosenblatt, J. S., & Komisaruk, B. R. (1977). Medial preoptic area and onset of maternal behavior in the rat. Journal of Comparative and Physiological Psychology, 91, 146164. doi:10.1037/h0077304CrossRefGoogle ScholarPubMed
O'Donnell, K. J., Glover, V., Barker, E. D., & O'Connor, T. G. (2014). The persisting effect of maternal mood in pregnancy on childhood psychopathology. Development and Psychopathology, 26, 393403. doi:10.1017/s0954579414000029CrossRefGoogle ScholarPubMed
O'Donnell, K. J., Glover, V., Jenkins, J., Browne, D., Ben-Shlomo, Y., Golding, J., & O'Connor, T. G. (2013). Prenatal maternal mood is associated with altered diurnal cortisol in adolescence. Psychoneuroendocrinology, 38, 16301638. doi:10.1016/j.psyneuen.2013.01.008CrossRefGoogle ScholarPubMed
Osborne, S., Biaggi, A., Chua, T. E., Du Preez, A., Hazelgrove, K., Nikkheslat, N., … Pariante, C. M. (2018). Antenatal depression programs cortisol stress reactivity in offspring through increased maternal inflammation and cortisol in pregnancy: The psychiatry research and motherhood - depression (PRAM-D) study. Psychoneuroendocrinology, 98, 211221. doi:10.1016/j.psyneuen.2018.06.017CrossRefGoogle ScholarPubMed
Posner, J., Cha, J., Wang, Z., Talati, A., Warner, V., Gerber, A., … Weissman, M. (2016). Increased default mode network connectivity in individuals at high familial risk for depression. Neuropsychopharmacology: Official Publication of the American College of Neuropsychopharmacology, 41(7), 17591767.10.1038/npp.2015.342CrossRefGoogle ScholarPubMed
Pearson, R. M., Evans, J., Kounali, D., Lewis, G., Heron, J., Ramchandani, P. G., … Stein, A. (2013). Maternal depression during pregnancy and the postnatal period: Risks and possible mechanisms for offspring depression at age 18 years. JAMA Psychiatry, 70, 13121319. doi:10.1001/jamapsychiatry.2013.2163CrossRefGoogle ScholarPubMed
Plant, D. T., Pariante, C. M., Sharp, D., & Pawlby, S. (2015). Maternal depression during pregnancy and offspring depression in adulthood: Role of child maltreatment. British Journal of Psychiatry, 207, 213220. doi:10.1192/bjp.bp.114.156620CrossRefGoogle ScholarPubMed
Pratchett, L. C., & Yehuda, R. (2011). Foundations of posttraumatic stress disorder: Does early life trauma lead to adult posttraumatic stress disorder? Development and Psychopathology, 23, 477491. doi:10.1017/S0954579411000186CrossRefGoogle ScholarPubMed
Racine, N. M., Madigan, S. L., Plamondon, A. R., McDonald, S. W., & Tough, S. C. (2018). Differential associations of adverse childhood experience on maternal health. American Journal of Preventive Medicine, 54, 368375. doi:10.1016/j.amepre.2017.10.028CrossRefGoogle ScholarPubMed
Racine, N., Plamondon, A., Madigan, S., McDonald, S., & Tough, S. (2018). Maternal adverse childhood experiences and infant development. Pediatrics, 141, e20172495. doi:10.1542/peds.2017-2495CrossRefGoogle ScholarPubMed
Racine, N., Zumwalt, K., McDonald, S., Tough, S., & Madigan, S. (2019). Perinatal depression: The role of maternal adverse childhood experiences and social support. Journal of Affective Disorders, 263, 576581. doi:10.1016/j.jad.2019.11.030CrossRefGoogle ScholarPubMed
Reuben, A., Moffitt, T. E., Caspi, A., Belsky, D. W., Harrington, H., Schroeder, F., … Danese, A. (2016). Lest we forget: Comparing retrospective and prospective assessments of adverse childhood experiences in the prediction of adult health. Journal of Child Psychology and Psychiatry, 57, 11031112. doi:10.1111/jcpp.12621CrossRefGoogle ScholarPubMed
Rhoades, G. K., Mazzoni, S., & O'Reilly Treter, M. (2019). Novel preventive interventions to promote relationship quality among diverse populations: Overview and results from four newly-developed programs. Paper presented at the annual meeting of the Association for Behavioral and Cognitive Therapies, Atlanta, GA.Google Scholar
Rice, F., Harold, G. T., Boivin, J., Hay, D. F., van den Bree, M., & Thapar, A. (2009). Disentangling prenatal and inherited influences in humans with an experimental design. Proceedings of the National Academy of Sciences of the United States of America, 106, 24642467. doi:10.1073/pnas.0808798106CrossRefGoogle ScholarPubMed
River, L. M., Narayan, A. J., Atzl, V. M., Rivera, L. M., & Lieberman, A. F. (2019). Past made present: The legacy of childhood maltreatment for romantic relationship quality and psychopathology during pregnancy. Psychology of Violence, 10(3), 324333. https://doi.org/10.1037/vio0000273CrossRefGoogle Scholar
River, L. M., Narayan, A. J., Atzl, V. M., Rivera, L. M., & Lieberman, A. F. (2020). Romantic partner support during pregnancy: The discrepancy between self-reported and coder-rated support as a risk factor for prenatal psychopathology and stress. Journal of Social and Personal Relationships, 37, 2746. doi:10.1177/0265407519850333CrossRefGoogle Scholar
River, L. M., Narayan, A. J., Galvan, T., Rivera, L. M., Harris, W. W., & Lieberman, A. F. (2019). On the verge of motherhood and mental illness: Prenatal mental health service utilization among women at highest risk. Zero to Three, 39, 3342.Google Scholar
Robinson, B. G., Emanuel, R. L., Frim, D. M., & Majzoub, J. A. (1988). Glucocorticoid stimulates expression of corticotropin-releasing hormone gene in human placenta. Proceedings of the National Academy of Sciences of the United States of America, 85, 52445248. doi:10.1073/pnas.85.14.5244CrossRefGoogle ScholarPubMed
Robinson, R., Lahti-Pulkkinen, M., Heinonen, K., Reynolds, R. M., & Raikkonen, K. (2019). Fetal programming of neuropsychiatric disorders by maternal pregnancy depression: A systematic mini review. Pediatric Research, 85, 134145. doi:10.1038/s41390-018-0173-yCrossRefGoogle ScholarPubMed
Rouse, M. H., & Goodman, S. H. (2014). Perinatal depression influences on infant negative affectivity: Timing, severity, and co-morbid anxiety. Infant Behavior and Development, 37, 739751. doi:10.1016/j.infbeh.2014.09.001CrossRefGoogle ScholarPubMed
Sandman, C. A., Buss, C., Head, K., & Davis, E. P. (2015). Fetal exposure to maternal depressive symptoms is associated with cortical thickness in late childhood. Biological Psychiatry, 77, 324334. doi:10.1016/j.biopsych.2014.06.025CrossRefGoogle ScholarPubMed
Sandman, C. A., Curran, M. M., Davis, E. P., Glynn, L. M., Head, K., & Baram, T. Z. (2018). Cortical thinning and neuropsychiatric outcomes in children exposed to prenatal adversity: A role for placental CRH? American Journal of Psychiatry, 175, 471479. doi:10.1176/appi.ajp.2017.16121433CrossRefGoogle ScholarPubMed
Sandman, C. A., Davis, E. P., Buss, C., & Glynn, L. M. (2011). Prenatal programming of human neurological function. International Journal of Peptides, 2011, 837596. doi:10.1155/2011/837596.CrossRefGoogle ScholarPubMed
Sandman, C. A., Davis, E. P., & Glynn, L. M. (2012). Prescient human fetuses thrive. Psychological Science, 23, 93100. doi:10.1177/0956797611422073CrossRefGoogle ScholarPubMed
Sandman, C. A., Glynn, L. M., & Davis, E. P. (2015). Neurobehavioral consequences of fetal exposure to gestational stress. In Kisilevsky, B., & Reissland, N. (Eds.), Advancing Research on Fetal Development. Cham, Switzerland: Springer Publisher.Google Scholar
Sandman, C. A., Glynn, L., Schetter, C. D., Wadhwa, P., Garite, T., Chicz-DeMet, A., & Hobel, C. (2006). Elevated maternal cortisol early in pregnancy predicts third trimester levels of placental corticotropin releasing hormone (CRH): Priming the placental clock. Peptides, 27, 14571463. doi:10.1016/j.peptides.2005.10.002CrossRefGoogle ScholarPubMed
Schreier, H. M., Enlow, M. B., Ritz, T., Gennings, C., & Wright, R. J. (2015). Childhood abuse is associated with increased hair cortisol levels among urban pregnant women. Journal of Epidemioogy and Community Health, 69, 11691174. doi:10.1136/jech-2015-205541CrossRefGoogle ScholarPubMed
Séguin, L., Potvin, L., Denis, M. S., & Loiselle, J. (1995). Chronic stressors, social support, and depression during pregnancy. Obstetrics & Gynecology, 85, 583589. doi:10.1016/0029-7844(94)00449-NCrossRefGoogle ScholarPubMed
Seng, J. S. (2002). A conceptual framework for research on lifetime violence, posttraumatic stress, and childbearing. Journal of Midwifery and Women's Health, 47, 337346. doi:10.1016/S1526-9523(02)00275-1CrossRefGoogle ScholarPubMed
Seng, J. S., Low, L. K., Ben-Ami, D., & Liberzon, I. (2010). Cortisol level and perinatal outcome in pregnant women with posttraumatic stress disorder: A pilot study. Journal of Midwifery & Women's Health, 50, 392398. doi:10.1016/j.jmwh.2005.04.024CrossRefGoogle Scholar
Seng, J. S., Low, L. K., Sperlich, M., Ronis, D. L., & Liberzon, I. (2011). Post-traumatic stress disorder, child abuse history, birthweight and gestational age: A prospective cohort study. BJOG: An International Journal of Obstetrics & Gynaecology, 118, 13291339. doi:10.1111/j.1471-0528.2011.03071.xCrossRefGoogle ScholarPubMed
Seng, J. S., Rauch, S. A., Resnick, H., Reed, C. D., King, A., Low, L. K., … Liberzon, I. (2010). Exploring posttraumatic stress disorder symptom profile among pregnant women. Journal of Psychosomatic Obstetrics & Gynecology, 31, 176187. doi:10.3109/0167482X.2010.486453CrossRefGoogle ScholarPubMed
Seng, J. S., Sperlich, M., Low, L. K., Ronis, D. L., Muzik, M., & Liberzon, I. (2013). Childhood abuse history, posttraumatic stress disorder, postpartum mental health, and bonding: A prospective cohort study. Journal of Midwifery & Women's Health, 58, 5768. doi:10.1111/j.1542-2011.2012.00237.xCrossRefGoogle ScholarPubMed
Shingo, T., Gregg, C., Enwere, E., Fujikawa, H., Hassam, R., Geary, C., … Weiss, S. (2003). Pregnancy-stimulated neurogenesis in the adult female forebrain mediated by prolactin. Science, 299, 117120. doi:10.1126/science.1076647CrossRefGoogle ScholarPubMed
Sidman, R. L., & Rakic, P. (1973). Neuronal migration, with special reference to developing human brain: A review. Brain Research, 62, 135. https://doi.org/10.1016/0006-8993(73)90617-3CrossRefGoogle ScholarPubMed
Slade, A., & Cohen, L. J. (1996). The process of parenting and the remembrance of things past. Infant Mental Health Journal, 17, 217238. doi:10.1002/(SICI)1097-0355(199623)17:3<217::AID-IMHJ3>3.0.CO;2-L3.0.CO;2-L>CrossRefGoogle Scholar
Slade, A., Cohen, L. J., Sadler, L. S., & Miller, M. (2009). The psychology and psychopathology of pregnancy. In Zeanah, C. H. (Ed.), Handbook of infant mental health (pp. 2239). New York, NY: Guilford Press.Google Scholar
Slattery, D. A., & Hillerer, K. M. (2016). The maternal brain under stress: Consequences for adaptive peripartum plasticity and its potential functional implications. Frontiers in Neuroendocrinology, 41, 114128. doi:10.1016/j.yfrne.2016.01.004CrossRefGoogle ScholarPubMed
Smith, R., Mesiano, S., & McGrath, S. (2002). Hormone trajectories leading to human birth. Regulatory Peptides, 108, 159164. doi:10.1016/S0167-0115(02)00105-2CrossRefGoogle ScholarPubMed
Sperlich, M., & Seng, J. S. (2008). Survivor moms: Women's stories of birthing, mothering and healing after sexual abuse. Eugene, OR: Motherbaby Press.Google Scholar
Stiles, J., & Jernigan, T. L. (2010). The basics of brain development. Neuropsychology Review, 20, 327348. https://doi.org/10.1007/s11065-010-9148-4CrossRefGoogle ScholarPubMed
Stout, S. A., Espel, E. V., Sandman, C. A., Glynn, L. M., & Davis, E. P. (2015). Fetal programming of children's obesity risk. Psychoneuroendocrinology, 53, 2939. doi:10.1016/j.psyneuen.2014.12.009CrossRefGoogle ScholarPubMed
Swales, D. A., Grande, L. A., Wing, D. A., Edelmann, M., Glynn, L. M., Sandman, C., … Davis, E. P. (2019). Can placental corticotropin-releasing hormone inform timing of antenatal corticosteroid administration? The Journal of Clinical Endocrinology and Metabolism, 104, 443450. doi:10.1210/jc.2018-00956CrossRefGoogle ScholarPubMed
Swales, D. A., Stout-Oswald, S. A., Glynn, L. M., Sandman, C., Wing, D. A., & Davis, E. P. (2018). Exposure to traumatic events in childhood predicts cortisol production among high risk pregnant women. Biological Psychology, 139, 186192. doi:10.1016/j.biopsycho.2018.10.006CrossRefGoogle ScholarPubMed
Thomas, J. C., Letourneau, N., Bryce, C. I., Campbell, T. S., Giesbrecht, G. F., & APrON Study Team. (2017). Biological embedding of perinatal social relationships in infant stress reactivity. Developmental Psychobiology, 59, 425435. doi:10.1002/dev.21505CrossRefGoogle ScholarPubMed
Thomason, M. E., Scheinost, D., Manning, J. H., Grove, L. E., Hect, J., Marshall, N., … Romero, R. (2017). Weak functional connectivity in the human fetal brain prior to preterm birth. Scientific Reports, 7, 39286. doi:10.1038/srep39286CrossRefGoogle ScholarPubMed
Tottenham, N. (2020). Early Adversity and the neotenous human brain. Biological Psychiatry, 87, 350358. doi:10.1016/j.biopsych.2019.06.018CrossRefGoogle ScholarPubMed
Van Batenburg-Eddes, T., Brion, M. J., Henrichs, J., Jaddoe, V. W. V., Hofman, A., Verhulst, F. C., … Tiemeier, H. (2013). Parental depressive and anxiety symptoms during pregnancy and attention problems in children: A cross-cohort consistency study. Journal of Child Psychology and Psychiatry, 54, 591600. doi:10.1111/jcpp.12023CrossRefGoogle ScholarPubMed
Van den Bergh, B. R., & Marcoen, A. (2004). High antenatal maternal anxiety is related to ADHD symptoms, externalizing problems, and anxiety in 8- and 9-year-olds. Child Development, 75, 10851097. doi:10.1111/j.1467-8624.2004.00727.xCrossRefGoogle ScholarPubMed
Van den Bergh, B. R., Mennes, M., Oosterlaan, J., Stevens, V., Stiers, P., Marcoen, A., & Lagae, L. (2005). High antenatal maternal anxiety is related to impulsivity during performance on cognitive tasks in 14- and 15-year-olds. Neuroscience & Biobehavioral Reviews, 29, 259269. doi:10.1016/j.neubiorev.2004.10.010CrossRefGoogle ScholarPubMed
Van den Bergh, B. R., Van Calster, B., Smits, T., Van Huffel, S., & Lagae, L. (2008). Antenatal maternal anxiety is related to HPA-axis dysregulation and self-reported depressive symptoms in adolescence: A prospective study on the fetal origins of depressed mood. Neuropsychopharmacology, 33, 536545. doi:10.1038/sj.npp.1301450CrossRefGoogle ScholarPubMed
Waffarn, F., & Davis, E. P. (2012). Effects of antenatal corticosteroids on the hypothalamic-pituitary-adrenocortical axis of the fetus and newborn: Experimental findings and clinical considerations. American Journal of Obstetrics & Gynecology, 207, 446454. doi:10.1016/j.ajog.2012.06.012CrossRefGoogle ScholarPubMed
Yehuda, R., Engel, S. M., Brand, S. R., Seckle, J., Marcus, S. M., & Berkowitz, G. S. (2005). Transgenerational effects of posttraumatic stress disorder in babies of mothers exposed to the World Trade Center attacks during pregnancy. Journal of Clinical Endocrinology & Metabolism, 90, 41154118. doi:10.1210/jc.2005-0550CrossRefGoogle Scholar
Yehuda, R., Flory, J. D., Pratchett, L. C., Buxbaum, J., Ising, M., & Holsboer, F. (2010). Putative biological mechanisms for the association between early life adversity and the subsequent development of PTSD. Psychopharmacology, 212, 405417. doi:10.1007/s00213-010-1969-6CrossRefGoogle ScholarPubMed
Yehuda, R., & Meaney, M. J. (2018). Relevance of psychological symptoms in pregnancy to intergenerational effects of preconception trauma. Biological Psychiatry, 83, 9496. doi:10.1016/j.biopsych.2017.10.027CrossRefGoogle ScholarPubMed
Yildiz, P. D., Ayers, S., & Phillips, L. (2017). The prevalence of posttraumatic stress disorder in pregnancy and after birth: A systematic review and meta-analysis. Journal of Affective Disorders, 208, 634645. doi:10.1016/j.jad.2016.10.009CrossRefGoogle ScholarPubMed
Yim, I. S., Glynn, L. M., Dunkel-Schetter, C., Hobel, C. J., Chicz-DeMet, A., & Sandman, C. A. (2009). Risk of postpartum depressive symptoms with elevated corticotropin-releasing hormone in human pregnancy. Arch Gen Psychiatry, 66, 162169. doi:10.1001/archgenpsychiatry.2008.533CrossRefGoogle ScholarPubMed
Yim, I. S., Glynn, L. M., Schetter, C. D., Hobel, C. J., Chicz-Demet, A., & Sandman, C. A. (2010). Prenatal beta-endorphin as an early predictor of postpartum depressive symptoms in euthymic women. Journal of Affective Disorders, 125, 128133. doi: 10.1016/j.jad.2009.12.009CrossRefGoogle ScholarPubMed