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Allostasis model facilitates understanding race differences in the diurnal cortisol rhythm

Published online by Cambridge University Press:  21 October 2011

Martie L. Skinner ,
Elizabeth A. Shirtcliff ,
Kevin P. Haggerty ,
Christopher L. Coe  and
Richard F. Catalano
Martie L. Skinner*
Affiliation:
University of Washington
Elizabeth A. Shirtcliff
Affiliation:
University of New Orleans
Kevin P. Haggerty
Affiliation:
University of Washington
Christopher L. Coe
Affiliation:
University of Wisconsin
Richard F. Catalano
Affiliation:
University of Washington
*
Address correspondence and reprint requests to: Martie L. Skinner, Social Development Research Group, University of Washington, 9725 3rd Avenue NE, Suite 401, Seattle, WA 98115; E-mail: skinnm@u.washington.edu.
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Abstract

The concept of allostasis suggests that greater cumulative stress burden can influence stress-responsive physiology. Dysregulation of allostatic mediators, including the hypothalamic–pituitary–adrenal (HPA) axis, is thought to precede many other signs of age-related pathology as the persistent burden of stressors accumulates over the individual's life span. We predicted that even in young adulthood, HPA regulation would differ between Blacks and Whites, reflecting, in part, higher rates of stressor exposure and greater potential for stressors to “get under the skin.” We examined whether stressor exposure, including experiences with racism and discrimination, explained race differences in waking cortisol and the diurnal rhythm. We also examined whether HPA functioning was associated with mental health outcomes previously linked to cortisol. Salivary cortisol was assayed in 275 young adults (127 Blacks, 148 Whites, 19 to 22 years old), four times a day across 3 days. Hierarchical linear models revealed flatter slopes for Blacks, reflecting significantly lower waking and higher bedtime cortisol levels compared to Whites. Associations of HPA functioning with stressors were typically more robust for Whites such that more stress exposure created an HPA profile that resembled that of Black young adults. For Blacks, greater stressor exposure did not further impact HPA functioning, or, when significant, was often associated with higher cortisol levels. Across both races, flatter slopes generally indicated greater HPA dysregulation and were associated with poor mental health outcomes. These differential effects were more robust for Whites. These findings support an allostatic model in which social contextual factors influence normal biorhythms, even as early as young adulthood.

Type
Articles
Information
Development and Psychopathology , Volume 23 , Issue 4: Allostatic Load: Part 2 , November 2011 , pp. 1167 - 1186
Copyright
Copyright © Cambridge University Press 2011

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References

Adam, E. K., Hawkley, L. C., Kudielka, B. M., & Cacioppo, J. T. (2006). Day-to-day dynamics of experience—Cortisol associations in a population-based sample of older adults. Proceedings of the National Academy of Sciences of the United States of America, 103, 17058–17063.CrossRefGoogle Scholar
Adinoff, B., Iranmanesh, A., Veldhuis, J., & Fisher, L. (1998). Disturbances of the stress response: The role of the HPA axis during alcohol withdrawal and abstinence. Alcohol Health and Research World, 22, 67–72.Google ScholarPubMed
Adinoff, B., Junghanns, K., Kiefer, F., & Krishnan-Sarin, S. (2005). Suppression of the HPA axis stress-response: Implications for relapse. Alcoholism: Clinical and Experimental Research, 29, 1351–1355.CrossRefGoogle ScholarPubMed
Adinoff, B., Risher-Flowers, D., De Jong, J., Ravitz, B., Bone, G. H., Nutt, D. J., et al. (1991). Disturbances of hypothalamic–pituitary–adrenal axis functioning during ethanol withdrawal in six men. American Journal of Psychiatry, 148, 1023–1025.Google ScholarPubMed
Alink, L. R., van Ijzendoorn, M. H., Bakermans-Kranenburg, M. J., Mesman, J., Juffer, F., & Koot, H. M. (2008). Cortisol and externalizing behavior in children and adolescents: Mixed meta-analytic evidence for the inverse relation of basal cortisol and cortisol reactivity with externalizing behavior. Developmental Psychobiology, 50, 427–450.CrossRefGoogle ScholarPubMed
Almeida, D. M., McGonagle, K., & King, H. (2009). Assessing daily stress processes in social surveys by combining stressor exposure and salivary cortisol. Biodemography and Social Biology, 55, 219–237.CrossRefGoogle ScholarPubMed
Antoni, M. H., Cruess, S., Cruess, D. G., Kumar, M., Lutgendorf, S., Ironson, G., et al. (2000). Cognitive–behavioral stress management reduces distress and 24-hour urinary free cortisol output among symptomatic HIV-infected gay men. Annals of Behavioral Medicine, 22, 29–37.CrossRefGoogle ScholarPubMed
Arnett, J.J. (2007). Emerging adulthood: What is it, and what is it good for? Child Development Perspectives, 1, 68–73.CrossRefGoogle Scholar
Barrett, Y. C., Akinsanya, B., Chang, S.-Y., & Vesterqvis, O. (2005). Automated on-line SPE LC-MS/MS method to quantitate 6beta-hydroxycortisol and cortisol in human urine: Use of the 6beta-hydroxycortisol to cortisol ratio as an indicator of CYP3A4 activity. Journal of Chromatography B, 821, 159–165.CrossRefGoogle ScholarPubMed
Bartels, M., de Geus, E. J., Kirschbaum, C., Sluyter, F., & Boomsma, D. I. (2003). Heritability of daytime cortisol levels in children. Behavior Genetics, 33, 421–433.CrossRefGoogle ScholarPubMed
Belsky, J., & Pluess, M. (2009). Beyond diathesis stress: Differential susceptibility to environmental influences. Psychological Bulletin, 135, 885–908.CrossRefGoogle ScholarPubMed
Bennett, G. G., Merritt, M. M., & Wolin, K. Y. (2004). Ethnicity, education, and the cortisol response to awakening: A preliminary investigation. Ethnicity & Health, 9, 337–347.CrossRefGoogle ScholarPubMed
Borrell, L. N., & Crawford, N. D. (2011). Social disparities in periodontitis among US adults: The effect of allostatic load. Journal of Epidemiology and Community Health, 65, 144–149.CrossRefGoogle ScholarPubMed
Boyce, W. T., & Ellis, B. J. (2005). Biological sensitivity to context: I. An evolutionary–developmental theory of the origins and functions of stress reactivity. Development and Psychopathology, 17, 271–301.CrossRefGoogle ScholarPubMed
Brody, G. H., Kogan, S. M., Chen, Y.-f., & Murry, V. M. (2008). Long-term effects of the strong African American families program on youths’ conduct problems. Journal of Adolescent Health, 43, 474–481.CrossRefGoogle ScholarPubMed
Bulatao, R. A., & Anderson, N. B. (Eds.). (2004). Understanding racial and ethnic differences in health in late life: A research agenda. Washington, DC: National Academies Press.Google Scholar
Burke, H. M., Davis, M. C., Otte, C., & Mohr, D. C. (2005). Depression and cortisol responses to psychological stress: A meta-analysis. Psychoneuroendocrinology, 30, 846–856.CrossRefGoogle ScholarPubMed
Buysse, D. J., Reynolds, C. F., Monk, T. H. 3rd, Berman, S. R., & Kupfer, D. J. (1989). The Pittsburgh Sleep Quality Index: A new instrument for psychiatric practice and research. Psychiatry Research, 28, 193–213.CrossRefGoogle ScholarPubMed
Carroll, J. F., Chiapa, A. L., Rodriquez, M., Phelps, D. R., Cardarelli, K. M., Vishwanatha, J. K., et al. (2008). Visceral fat, waist circumference, and BMI: Impact of race/ethnicity. Obesity, 16, 600–607.CrossRefGoogle ScholarPubMed
Caughy, M. O. B., O'Campo, P. J., & Muntaner, C. (2003). When being alone might be better: Neighborhood poverty, social capital, and child mental health. Social Science & Medicine, 57, 227–237.CrossRefGoogle ScholarPubMed
Cicchetti, D., & Cohen, D. J. (Eds.). (1995). Developmental psychopathology: Vol. 1. Theory and methods. Oxford: Wiley.Google Scholar
Cicchetti, D., & Curtis, W. J. (2007). Multilevel perspectives on pathways to resilient functioning. Development and Psychopathology, 19, 627–629.CrossRefGoogle ScholarPubMed
Cicchetti, D., & Lynch, M. (1995). Failures in the expectable environment and their impact on individual development: The case of child maltreatment. In D. Cicchetti & D. J. Cohen (Eds.), Developmental psychopathology: Vol. 2. Risk, disorders, and adaptation (pp. 32–71). Oxford: Wiley.Google Scholar
Cicchetti, D., & Rogosch, F. A. (1999). Psychopathology as risk for adolescent substance use disorders: A developmental psychopathology perspective. Journal of Clinical Child Psychology, 28, 355–365.CrossRefGoogle ScholarPubMed
Cicchetti, D., & Rogosch, F. A. (2001). Diverse patterns of neuroendocrine activity in maltreated children. Development and Psychopathology, 13, 677–693.CrossRefGoogle ScholarPubMed
Cicchetti, D., & Rogosch, F. A. (2007). Personality, adrenal steroid hormones, and resilience in maltreated children: A multilevel perspective. Development and Psychopathology, 19, 787–809.CrossRefGoogle ScholarPubMed
Cicchetti, D., & Toth, S. L. (2009). The past achievements and future promises of developmental psychopathology: The coming of age of a discipline. Journal of Child Psychology and Psychiatry, 50, 16–25.CrossRefGoogle ScholarPubMed
Cohen, S., Schwartz, J. E., Epel, E., Kirschbaum, C., Sidney, S., & Seeman, T. (2006). Socioeconomic status, race and diurnal cortisol decline in the Coronary Artery Risk Development in Young Adults (CARDIA) study. Psychosomatic Medicine, 68, 41–50.CrossRefGoogle ScholarPubMed
Conger, R. D., Conger, K. J., Elder, G. H., Lorenz, F. O., Simons, R. L., & Whitbeck, L. B. (1992). A family process model of economic hardship and adjustment of early adolescent boys. Child Development, 63, 526–541.CrossRefGoogle ScholarPubMed
Croissant, B., & Olbrich, R. (2004). Stress response dampening indexed by cortisol in subjects at risk for alcoholism. Journal of Studies on Alcohol, 65, 701–707.CrossRefGoogle ScholarPubMed
Cunradi, C. B., Caetano, R., Clark, C., & Schafer, J. (2000). Neighborhood poverty as a predictor of intimate partner violence among White, Black, and Hispanic couples in the United States: A multilevel analysis. Annals of Epidemiology, 10, 297–308.CrossRefGoogle ScholarPubMed
Dallman, M. F., Viau, V., Bhatnagar, S., Gomez, F., Laugero, K., & Bell, M. E. (2002). Corticotropin-releasing factor (CRF), corticosteroids, stress and sugar: Energy balance the brain and behavior. In Pfaff, D. (Ed.), Hormones, brain and behavior (Vol. 1, pp. 571–631). San Diego, CA: Academic Press.CrossRefGoogle Scholar
De Kloet, E. R. (2004). Hormones and the stressed brain. Annals of the New York Academy of Sciences, 1018, 1–15.CrossRefGoogle ScholarPubMed
Decety, J., & Lamm, C. (2006). Human empathy through the lens of social neuroscience. Scientific World Journal, 6, 1146–1163.CrossRefGoogle ScholarPubMed
Del Guidice, M., Ellis, B. J., & Shirtcliff, E. A. (2011). The adaptive calibration of stress responsivity. Neuroscience and Behavioral Reviews, 35, 1562–1592.CrossRefGoogle Scholar
Derogatis, L. R. (1993). BSI, Brief Symptom Inventory: Administration, scoring & procedures manual. Minneapolis, MN: National Computer Systems.Google Scholar
DeSantis, A. S., Adam, E. K., Doane, L. D., Mineka, S., Zinbarg, R. E., & Craske, M. G. (2007). Racial/ethnic differences in cortisol diurnal rhythms in a community sample of adolescents. Journal of Adolescent Health, 41, 3–13.CrossRefGoogle Scholar
Dickerson, S. S., & Kemeny, M. E. (2004). Acute stressors and cortisol responses: A theoretical integration and synthesis of laboratory research. Psychological Bulletin, 130, 355–391.CrossRefGoogle ScholarPubMed
Dozier, M., Manni, M., Gordon, M. K., Peloso, E., Gunnar, M. R., Stovall-McClough, K. C., et al. (2006). Foster children's diurnal production of cortisol: An exploratory study. Child Maltreatment, 11, 189–197.CrossRefGoogle ScholarPubMed
Duncan, G. J., & Brooks-Gunn, J. (Eds.). (1997). Consequences of growing up poor. New York: Russell Sage Foundation.Google Scholar
Duncan, S. C., Duncan, T. E., & Strycker, L. A. (2002). A multilevel analysis of neighborhood context and youth alcohol and drug problems. Prevention Science, 3, 125–133.CrossRefGoogle ScholarPubMed
Ellis, B. J., & Boyce, W. T. (2011). Differential susceptibility to the environment: Toward an understanding of sensitivity to developmental experiences and context. Development and Psychopathology, 23, 1–5.CrossRefGoogle Scholar
Ellis, B. J., Boyce, W. T., Belsky, J., Bakermans-Kranenburg, M. J., & van IJzendoorn, M. H. (2011). Differential susceptibility to the environment: An evolutionary–neurodevelopmental theory. Development and Psychopathology, 23, 7–28.CrossRefGoogle Scholar
Ellis, B. J., Essex, M. J., & Boyce, W. T. (2005). Biological sensitivity to context: II. Empirical explorations of an evolutionary–developmental theory. Development and Psychopathology, 17, 303–328.CrossRefGoogle ScholarPubMed
Essex, M. J., Armstrong, J. M., Burk, L. R., Goldsmith, H. H., & Boyce, W. T. (2011). Biological sensitivity to context moderates the effects of the early teacher–child relationship on the development of mental health by adolescence. Development and Psychopathology, 23, 149–161.CrossRefGoogle ScholarPubMed
Essex, M. J., Shirtcliff, E. A., Burk, L. R., Ruttle, P. L., Klein, M. H., Slattery, M. J., et al. (2011). Influence of early life stress on later hypothalamic–pituitary–adrenal functioning and its covariation with mental health symptoms: A study of the allostatic process from childhood into adolescence. Development and Psychopathology, 23, 1039–1058.CrossRefGoogle ScholarPubMed
Evans, G. W. (2003). A multimethodological analysis of cumulative risk and allostatic load among rural children. Developmental Psychology, 39, 924–933.CrossRefGoogle ScholarPubMed
Evans, G. W., & English, K. (2002). The environment of poverty: Multiple stressor exposure, psychophysiological stress, and socioemotional adjustment. Child Development, 73, 1238–1248.CrossRefGoogle ScholarPubMed
Evans, G. W., Lercher, P., Meis, M., Ising, H., & Kofler, W. W. (2001). Community noise exposure and stress in children. Journal of the Acoustical Society of America, 109, 1023–1027.CrossRefGoogle ScholarPubMed
Fernades, A., Skinner, M. L., Woelfel, T., Carpenter, T., & Haggerty, K. P. (in press). Implementing self-collecting of biological specimens with a diverse sample. Field Methods.Google Scholar
Fisher, P. A., Gunnar, M. R., Chamberlain, P., & Reid, J. B. (2000). Preventive intervention for maltreated preschool children: Impact on children's behavior, neuroendocrine activity, and foster parent functioning. Journal of the American Academy of Child & Adolescent Psychiatry, 39, 1356–1364.CrossRefGoogle ScholarPubMed
Fisher, P. A., Stoolmiller, M., Gunnar, M. R., & Burraston, B. O. (2007). Effects of a therapeutic intervention for foster preschoolers on diurnal cortisol activity. Psychoneuroendocrinology, 32, 892–905.CrossRefGoogle ScholarPubMed
Fisher, P. A., Van Ryzin, M. J., & Gunnar, M. R. (2011). Mitigating HPA axis dysregulation associated with placement changes in foster care. Psychoneuroendocrinology, 36, 531–539.CrossRefGoogle ScholarPubMed
Geronimus, A. T., Hicken, M., Keene, D., & Bound, J. (2006). “Weathering” and age patterns of allostatic load scores among Blacks and Whites in the United States. American Journal of Public Health, 96, 826–833.CrossRefGoogle ScholarPubMed
Granger, D. A., Blair, C., Willoughby, M., Kivlighan, K. T., Hibel, L. C., Fortunato, C. K., et al. (2007). Individual differences in salivary cortisol and alpha-amylase in mothers and their infants: Relation to tobacco smoke exposure. Developmental Psychobiology, 49, 692–701.CrossRefGoogle ScholarPubMed
Gray, M. J., Litz, B. T., Hsu, J. L., & Lombardo, T. W. (2004). Psychometric properties of the life events checklist. Assessment, 11, 330–341.CrossRefGoogle ScholarPubMed
Green, T. L., & Darity, W. A. Jr. (2010). Under the skin: Using theories from biology and the social sciences to explore the mechanisms behind the Black–White health gap. American Journal of Public Health, 100, S36–S40.CrossRefGoogle ScholarPubMed
Gunnar, M. R., Talge, N. M., & Herrera, A. (2009). Stressor paradigms in developmental studies: What does and does not work to produce mean increases in salivary cortisol. Psychoneuroendocrinology, 34, 953–967.CrossRefGoogle Scholar
Gunnar, M. R., Tout, K., de Haan, M., Pierce, S., & Stansbury, K. (1997). Temperament, social competence, and adrenocortical activity in preschoolers. Developmental Psychobiology, 31, 65–85.3.0.CO;2-S>CrossRefGoogle ScholarPubMed
Gunnar, M. R., & Vazquez, D. M. (2001). Low cortisol and a flattening of expected daytime rhythm: Potential indices of risk in human development. Development and Psychopathology, 13, 515–538.CrossRefGoogle Scholar
Hagan, M. J., Luecken, L. J., Sandler, I. N., & Tien, J. (2010). Prospective effects of post-bereavement negative events on cortisol activity in parentally bereaved youth. Developmental Psychobiology, 52, 394–400.CrossRefGoogle ScholarPubMed
Haggerty, K. P., MacKenzie, E. P., Skinner, M. L., Harachi, T. W., & Catalano, R. F. (2006). Participation in “Parents Who Care”: Predicting program initiation and exposure in two different program formats. Journal of Primary Prevention, 27, 47–65.CrossRefGoogle ScholarPubMed
Haggerty, K. P., Skinner, M. L., MacKenzie, E. P., & Catalano, R. F. (2007). A randomized trial of Parents Who Care: Effects on key outcomes at 24-month follow-up. Prevention Science, 8, 249–260.CrossRefGoogle Scholar
Harrell, S. P. (2000). A multidimensional conceptualization of racism-related stress: Implications for the well-being of people of color. American Journal of Orthopsychiatry, 70, 42–57.CrossRefGoogle ScholarPubMed
Harrell, S. P., Merchant, M., & Young, S. A. (1997). Psychometric properties of the Racism and Life Experience Scales (RaLES). Unpublished manuscript.Google Scholar
Hastings, P. D., Shirtcliff, E. A., Klimes-Dougan, B., Allison, A. L., DeRose, L., Usher, B., et al. (2011). Allostasis and the development of internalizing and externalizing problems: Changing relations with physiological systems across adolescence. Development and Psychopathology.CrossRefGoogle ScholarPubMed
Hawes, D. J., Brennan, J., & Dadds, M. R. (2009). Cortisol, callous-unemotional traits, and pathways to antisocial behavior. Current Opinion in Psychiatry, 22, 357–362.CrossRefGoogle ScholarPubMed
Hawkins, J. D., Kosterman, R., Catalano, R. F., Hill, K. G., & Abbott, R. D. (2005). Promoting positive adult functioning through social development intervention in childhood: Long-term effects from the Seattle Social Development Project. Archives of Pediatrics and Adolescent Medicine, 159, 25–31.CrossRefGoogle ScholarPubMed
Heinrichs, M., Baumgartner, T., Kirschbaum, C., & Ehlert, U. (2003). Social support and oxytocin interact to suppress cortisol and subjective responses to psychosocial stress. Biological Psychiatry, 54, 1389–1298.CrossRefGoogle ScholarPubMed
Heron, M. (2007). Deaths: Leading causes for 2004. Hyattsville, MD: US Department of Health and Human Services.Google ScholarPubMed
Het, S., Rohleder, N., Schoofs, D., Kirschbaum, C., & Wolf, O. T. (2009). Neuroendocrine and psychometric evaluation of a placebo version of the “Trier Social Stress Test.” Psychoneuroendocrinology, 34, 1075–1086.CrossRefGoogle ScholarPubMed
Hogle, J. M., & Curtin, J. J. (2006). Sex differences in negative affective response during nicotine withdrawal. Psychophysiology, 43, 344–356.CrossRefGoogle ScholarPubMed
Huffman, R. (2009). Metabolic syndrome racial differences in adolescents. Current Diabetes Reviews, 5, 259–265.CrossRefGoogle Scholar
Johnston-Brooks, C. H., Lewis, M. A., Evans, G. W., & Whalen, C. K. (1998). Chronic stress and illness in children: The role of allostatic load. Psychosomatic Medicine, 60, 597–603.CrossRefGoogle ScholarPubMed
Kaholokula, J. K., Grandinetti, A., Keller, S., Nacapoy, A. H., Kingi, T. K., & Mau, M. K. (2011). Association between perceived racism and physiological stress indices in Native Hawaiians. Journal of Behavioral Medicine. doi:10.1007/s10865-011-9330-zGoogle ScholarPubMed
Karlamangla, A. S., Merkin, S. S., Crimmins, E. M., & Seeman, T. E. (2010). Socioeconomic and ethnic disparities in cardiovascular risk in the United States, 2001–2006. Annals of Epidemiology, 20, 617–628.CrossRefGoogle ScholarPubMed
Kessler, R. C., Berglund, P., Demler, O., Jin, R., & Walters, E. E. (2005). Lifetime prevalence and age-of-onset distributions of DSM-IV disorders in the National Comorbidity Survey Replication. Archives of General Psychiatry, 62, 593–602.CrossRefGoogle ScholarPubMed
Keyes, C. L. (2009). The Black–White paradox in health: Flourishing in the face of social inequality and discrimination. Journal of Personality, 77, 1677–1706.CrossRefGoogle ScholarPubMed
Kirschbaum, C., Klauer, T., Filipp, S. H., & Hellhammer, D. H. (1995). Sex-specific effects of social support on cortisol and subjective responses to acute psychological stress. Psychosomatic Medicine, 57, 23–31.CrossRefGoogle ScholarPubMed
Knafo, A., Israel, S., & Ebstein, R. P. (2011). Heritability of children's prosocial behavior and differential susceptibility to parenting by variation in the dopamine receptor D4 gene. Development and Psychopathology, 23, 53–67.CrossRefGoogle ScholarPubMed
Koob, G. F., & Le Moal, M. (2001). Drug addiction, dysregulation of reward, and allostasis. Neuropsychopharmacology, 24, 97–129.CrossRefGoogle ScholarPubMed
Koob, G. F., & Le Moal, M. (2008a). Addiction and the brain antireward system. Annual Review of Psychology, 59, 29–53.CrossRefGoogle ScholarPubMed
Koob, G. F., & Le Moal, M. (2008b). Review. Neurobiological mechanisms for opponent motivational processes in addiction. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, 363, 3113–3123.CrossRefGoogle ScholarPubMed
Korte, S. M., Koolhaas, J. M., Wingfield, J. C., & McEwen, B. S. (2005). The Darwinian concept of stress: Benefits of allostasis and costs of allostatic load and the trade-offs in health and disease. Neuroscience and Biobehavioral Reviews, 29, 3–38.CrossRefGoogle ScholarPubMed
Krieger, N. (2005). Embodiment: A conceptual glossary for epidemiology. Journal of Epidemiology and Community Health, 59, 350–355.CrossRefGoogle ScholarPubMed
Lam, S., Dickerson, S. S., Zoccola, P. M., & Zaldivar, F. (2009). Emotion regulation and cortisol reactivity to a social-evaluative speech task. Psychoneuroendocrinology, 34, 1355–1362.CrossRefGoogle ScholarPubMed
Landrine, H., & Klonoff, E. A. (1996). The schedule of racist events: A measure of racial discrimination and a study of its negative physical and mental health consequences. Journal of Black Psychology, 22, 144–168.CrossRefGoogle Scholar
Lantz, P. M., House, J. S., Mero, R. P., & Williams, D. R. (2005). Stress, life events, and socioeconomic disparities in health: Results from the Americans’ Changing Lives Study. Journal of Health and Social Behavior, 46, 274–288.CrossRefGoogle ScholarPubMed
Loney, B. R., Butler, M. A., Lima, E. N., Counts, C. A., & Eckel, L. A. (2006). The relation between salivary cortisol, callous-unemotional traits, and conduct problems in an adolescent non-referred sample. Journal of Child Psychology and Psychiatry and Allied Disciplines, 47, 30–36.CrossRefGoogle Scholar
Lovallo, W. R. (2006). Cortisol secretion patterns in addiction and addiction risk. International Journal of Psychophysiology, 59, 195–202.CrossRefGoogle ScholarPubMed
Luecken, L. J., Hagan, M. J., Sandler, I. N., Tien, J., Ayers, T. S., & Wolchik, S. A. (2009). Cortisol levels six-years after participation in the Family Bereavement Program. Psychoneuroendocrinology, 35, 785–789.CrossRefGoogle ScholarPubMed
Lupien, S. J., King, S., Meaney, M. J., & McEwen, B. S. (2000). Child's stress hormone levels correlate with mother's socioeconomic status and depressive state. Biological Psychiatry, 48, 976–980.CrossRefGoogle ScholarPubMed
Lupien, S. J., King, S., Meaney, M. J., & McEwen, B. S. (2001). Can poverty get under your skin? Basal cortisol levels and cognitive function in children from low and high socioeconomic status. Development and Psychopathology, 13, 653–676.CrossRefGoogle ScholarPubMed
Lupien, S. J., Ouellet-Morin, I., Hupbach, A., Tu, M. T., Buss, C., Walker, D., et al. (2006). Beyond the stress concept: Allostatic load—A developmental biological and cognitive perspective. In Cicchetti, D. & Cohen, D. J. (Eds.), Developmental psychopathology: Vol. 2. Developmental neuroscience (2nd ed., pp. 578–628). New York: Wiley.Google Scholar
Luthar, S. S. (2006). Resilience in development: A synthesis of research across five decades. In Cicchetti, D. & Cohen, D. J. (Eds.), Developmental psychopathology: Risk, disorder, and adaptation (2nd ed., pp. 739–795). New York: Wiley.Google Scholar
Lyons, D. M., & Parker, K. J. (2007). Stress inoculation-induced indications of resilience in monkeys. Journal of Traumatic Stress, 20, 423–433.CrossRefGoogle ScholarPubMed
Massey, D. S. (2004). Segregation and stratification: A biosocial perspective. Du Bois Review: Social Science Research on Race, 1, 7–25.CrossRefGoogle Scholar
McBurnett, K., Raine, A., Stouthamer-Loeber, M., Loeber, R., Kumar, A. M., Kumar, M., et al. (2005). Mood and hormone responses to psychological challenge in adolescent males with conduct problems. Biological Psychiatry, 57, 1109–1116.CrossRefGoogle ScholarPubMed
McEwen, B. S. (1998). Stress, adaptation, and disease: Allostasis and allostatic load. Annals of the New York Academy of Sciences, 840, 33–44.CrossRefGoogle ScholarPubMed
McEwen, B. S. (2000a). Allostasis, allostatic load, and the aging nervous system: Role of excitatory amino acids and excitotoxicity. Neurochemical Research, 25, 1219–1231.CrossRefGoogle ScholarPubMed
McEwen, B. S. (2000b). The neurobiology of stress: From serendipity to clinical relevance. Brain Research, 886, 172–189.CrossRefGoogle ScholarPubMed
McEwen, B. S. (2000c). Protective and damaging effects of stress mediators: Central role of the brain. Progress in Brain Research, 122, 25–34.CrossRefGoogle ScholarPubMed
McEwen, B. S. (2003). Mood disorders and allostatic load. Biological Psychiatry, 54, 200–207.CrossRefGoogle ScholarPubMed
Merritt, M. M., McCallum, T. J., & Fritsch, T. (2011). How much striving is too much? John henryism active coping predicts worse daily cortisol responses for African American but not white female dementia family caregivers. American Journal of Geriatric Psychiatry, 19, 451–460.CrossRefGoogle Scholar
Miller, G. E., Chen, E., & Zhou, E. S. (2007). If it goes up, must it come down? Chronic stress and the hypothalamic–pituitary–adrenocortical axis in humans. Psychological Bulletin, 133, 25–45.CrossRefGoogle ScholarPubMed
Moons, W. G., Eisenberger, N. I., & Taylor, S. E. (2009). Anger and fear responses to stress have different biological profiles. Brain, Behavior, and Immunity, 24, 215–219.CrossRefGoogle ScholarPubMed
Moss, H. B., Vanyukov, M., Yao, J. K., & Kirillova, G. P. (1999). Salivary cortisol responses in prepubertal boys: The effects of parental substance abuse and association with drug use behavior during adolescence. Biological Psychiatry, 45, 1293–1299.CrossRefGoogle ScholarPubMed
Moss, H. B., Vanyukov, M. M., & Martin, C. S. (1995). Salivary cortisol responses and the risk for substance abuse in prepubertal boys. Biological Psychiatry, 38, 547–555.CrossRefGoogle ScholarPubMed
Munro, C., & Stabenfeldt, G. H. (1985). Development of a cortisol enzyme-immunoassay in plasma. Clinical Chemistry, 31, 956.Google Scholar
O'Connor, K. A., Brindle, E., Holman, D. J., Klein, N. A., Soules, M. R., Campbell, K. L., et al. (2003). Urinary estrone conjugate and pregnanediol 3-glucuronide enzyme immunoassays for population research. Clinical Chemistry, 49, 1139–1148.CrossRefGoogle ScholarPubMed
O'Leary, M. M., Loney, B. R., & Eckel, L. A. (2007). Gender differences in the association between psychopathic personality traits and cortisol response to induced stress. Psychoneuroendocrinology, 32, 183–191.CrossRefGoogle ScholarPubMed
Obradovic, J., & Boyce, W. T. (2009). Individual differences in behavioral, physiological, and genetic sensitivities to contexts: Implications for development and adaptation. Developmental Neuroscience, 31, 300–308.CrossRefGoogle ScholarPubMed
Obradovic, J., Bush, N. R., & Boyce, W. T. (2011). The interactive effect of marital conflict and stress reactivity on externalizing and internalizing symptoms: The role of laboratory stressors. Development and Psychopathology, 23, 101–114.CrossRefGoogle ScholarPubMed
Obradovic, J., Bush, N. R., Stamperdahl, J., Adler, N. E., & Boyce, W. T. (2010). Biological sensitivity to context: The interactive effects of stress reactivity and family adversity on socioemotional behavior and school readiness. Child Development, 81, 270–289.CrossRefGoogle ScholarPubMed
Ockenfels, M. C., Porter, L., Smyth, J., Kirschbaum, C., Hellhammer, D. H., & Stone, A. A. (1995). Effect of chronic stress associated with unemployment on salivary cortisol: Overall cortisol levels, diurnal rhythm, and acute stress reactivity. Psychosomatic Medicine, 57, 460–467.CrossRefGoogle ScholarPubMed
Oosterlaan, J., Geurts, H. M., Knol, D. L., & Sergeant, J. A. (2005). Low basal salivary cortisol is associated with teacher-reported symptoms of conduct disorder. Psychiatry Research, 134, 1–10.CrossRefGoogle ScholarPubMed
Parker, K. J., Buckmaster, C. L., Schatzberg, A. F., & Lyons, D. M. (2004). Prospective investigation of stress inoculation in young monkeys. Archives of General Psychiatry, 61, 933–941.CrossRefGoogle ScholarPubMed
Paschall, M. J., Flewelling, R. L., & Ennett, S. T. (1998). Racial differences in violent behavior among young adults: Moderating and confounding effects. Journal of Research in Crime and Delinquency, 35, 148–165.CrossRefGoogle Scholar
Peeters, F., Nicholson, N. A., & Berkhof, J. (2003). Cortisol responses to daily events in major depressive disorder. Psychosomatic Medicine, 65, 836–841.CrossRefGoogle ScholarPubMed
Peters, M. F., & Massey, G. (1983). Mundane extreme environmental stress in family stress theories: The case of Black families in White America. Marriage & Family Review, 6, 193–218.CrossRefGoogle Scholar
Phan, K. L., Wager, T., Taylor, S. F., & Liberzon, I. (2002). Functional neuroanatomy of emotion: A meta-analysis of emotion activation studies in PET and fMRI. NeuroImage, 16, 331–348.CrossRefGoogle ScholarPubMed
Piazza, P. V., & Le Moal, M. (1996). Pathophysiological basis of vulnerability to drug abuse: Role of an interaction between stress, glucocorticoids, and dopaminergic neurons. Annual Review of Pharmacology and Toxicology, 36, 359–378.CrossRefGoogle ScholarPubMed
Popma, A., Doreleijers, T. A., Jansen, L. M., Van Goozen, S. H., Van Engeland, H., & Vermeiren, R. (2007). The diurnal cortisol cycle in delinquent male adolescents and normal controls. Neuropsychopharmacology, 32, 1622–1628.CrossRefGoogle ScholarPubMed
Prelow, H. M., Danoff-Burg, S., Swenson, R. R., & Pulgiano, D. (2004). The impact of ecological risk and perceived discrimination on the psychological adjustment of African American and European American youth. Journal of Community Psychology, 32, 375–389.CrossRefGoogle Scholar
Pruessner, J. C., Dedovic, K., Pruessner, M., Lord, C., Buss, C., Collins, L., et al. (2010). Stress regulation in the central nervous system: Evidence from structural and functional neuroimaging studies in human populations—2008 Curt Richter Award Winner. Psychoneuroendocrinology, 35, 179–191.CrossRefGoogle ScholarPubMed
Raine, A. (2002). Biosocial studies of antisocial and violent behavior in children and adults: A review. Journal of Abnormal Child Psychology, 30, 311–326.CrossRefGoogle ScholarPubMed
Richman, L. S., & Jonassaint, C. (2008). The effects of race-related stress on cortisol reactivity in the laboratory: Implications of the Duke lacrosse scandal. Annals of Behavioral Medicine, 35, 105–110.CrossRefGoogle ScholarPubMed
Rosmalen, J. G., Oldehinkel, A. J., Ormel, J., de Winter, A. F., Buitelaar, J. K., & Verhulst, F. C. (2005). Determinants of salivary cortisol levels in 10–12 year old children: A population-based study of individual differences. Psychoneuroendocrinology, 30, 483–495.CrossRefGoogle ScholarPubMed
Roy, M. P., Steptoe, A., & Kirschbaum, C. (1998). Life events and social support as moderators of individual differences in cardiovascular and cortisol reactivity. Journal of Personality and Social Psychology, 75, 1273–1281.CrossRefGoogle ScholarPubMed
Ruttle, P. L., Shirtcliff, E. A., Serbin, L. A., Ben-Dat Fisher, D., Stack, D. M., & Schwartzman, A. E. (2011). Disentangling psychobiological mechanisms underlying internalizing and externalizing behaviors in youth: Longitudinal and concurrent associations with cortisol. Hormones and Behavior, 59, 123–132.CrossRefGoogle ScholarPubMed
Sapolsky, R. M. (1998). Why zebras don't get ulcers: An updated guide to stress, stress-related diseases, and coping. New York: W.H. Freeman.Google Scholar
Sapolsky, R. M., Romero, L. M., & Munck, A. U. (2000). How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions. Endocrine Reviews, 21, 55–89.Google ScholarPubMed
Schreiber, J. E., Shirtcliff, E., Van Hulle, C., Lemery-Chalfant, K., Klein, M. H., Kalin, N. H., et al. (2006). Environmental influences on family similarity in afternoon cortisol levels: twin and parent–offspring designs. Psychoneuroendocrinology, 31, 1131–1137.CrossRefGoogle ScholarPubMed
Schulenberg, J.E., Sameroff, A.J., & Cicchetti, D. (2004). The transition to adulthood as a critical juncture in the course of psychopathology and mental health. Development and Psychopathology, 16, 799–806.CrossRefGoogle ScholarPubMed
Schulkin, J., McEwen, B. S., & Gold, P. W. (1994). Allostasis, amygdala, and anticipatory angst. Neuroscience and Biobehavioral Reviews, 18, 385–396.CrossRefGoogle ScholarPubMed
Selye, H. (1950). Stress: The physiology and pathology of exposure to stress. Montreal: Acta Medical Publishers.Google Scholar
Sethre-Hofstad, L., Stansbury, K., & Rice, M. A. (2002). Attunement of maternal and child adrenocortical response to child challenge. Psychoneuroendocrinology, 27, 731–747.CrossRefGoogle ScholarPubMed
Shirtcliff, E. A., Allison, A. L., Armstrong, J. M., Slattery, M., Kalin, N. H., & Essex, M. J. (2011). Longitudinal stability and developmental properties of salivary cortisol levels and diurnal rhythms from childhood to adolescence. Unpublished manuscript.Google ScholarPubMed
Shirtcliff, E. A., & Essex, M. J. (2008). Concurrent and longitudinal associations of basal and diurnal cortisol with mental health symptoms in early adolescence. Developmental Psychobiology, 50, 690–703.CrossRefGoogle ScholarPubMed
Shirtcliff, E. A., Granger, D. A., Booth, A., & Johnson, D. (2005). Low salivary cortisol levels and externalizing behavior problems in youth. Development and Psychopathology, 17, 167–184.CrossRefGoogle ScholarPubMed
Shirtcliff, E. A., Vitacco, M. J., Graf, A. R., Gostisha, A. J., Merz, J. L., & Zahn-Waxler, C. (2009). Neurobiology of empathy and callousness: Implications for the development of antisocial behavior. Behavioral Sciences & the Law, 27, 137–171.CrossRefGoogle ScholarPubMed
Siever, L. J., & Davis, K. L. (1985). Overview: Toward a dysregulation hypothesis of depression. American Journal of Psychiatry, 142, 1017–1031.Google Scholar
Simons, R. L., Murry, V., McLoyd, V., Lin, K.-H., Cutrona, C., & Conger, R. D. (2002). Discrimination, crime, ethnic identity, and parenting as correlates of depressive symptoms among African American children: A multilevel analysis. Development and Psychopathology, 14, 371–393.CrossRefGoogle ScholarPubMed
Singer, J. D. (1998). Using SAS PROC MIXED to fit multilevel models, hierarchical models, and individual growth models. Journal of Educational and Behavioral Statistics, 23, 323–355.CrossRefGoogle Scholar
Singer, T., Seymour, B., O'Doherty, J., Kaube, H., Dolan, R. J., & Frith, C. D. (2004). Empathy for pain involves the affective but not sensory components of pain. Science, 303, 1157–1162.CrossRefGoogle Scholar
Stone, A. A., Schwartz, J. E., Smyth, J., Kirschbaum, C., Cohen, S., Hellhammer, D., et al. (2001). Individual differences in the diurnal cycle of salivary free cortisol: A replication of flattened cycles for some individuals. Psychoneuroendocrinology, 26, 295–306.CrossRefGoogle ScholarPubMed
Straus, M. A. (1990). The Conflict Tactics Scale and its critics: An evaluation and new data on validity and reliability. In Straus, M. A. & Gelles, R. J. (Eds.), Physical violence in American families: Risk factors and adaptations to violence in 8,145 families (pp. 49–73). New Brunswick, NJ: Transaction Publishing.Google Scholar
Susman, E. J. (2006). Psychobiology of persistent antisocial behavior: Stress, early vulnerabilities and the attenuation hypothesis. Neuroscience and Behavioral Reviews, 30, 376–389.CrossRefGoogle ScholarPubMed
Szalacha, L. A., Erkut, S., Garcia Coll, C., Fields, J. P., Alarcon, O., & Ceder, I. (2003). Perceived discrimination and resilience. In Luthar, S. S. (Ed.), Resilience and vulnerability: Adaptation in the context of childhood adversity (pp. 414–435). New York: Cambridge University Press.CrossRefGoogle Scholar
Szanton, S. L., Gill, J. M., & Allen, J. K. (2005). Allostatic load: A mechanism of socioeconomic health disparities? Biological Research For Nursing, 7, 7–15.CrossRefGoogle ScholarPubMed
Taylor, S. E., Burklund, L. J., Eisenberger, N. I., Lehman, B. J., Hilmert, C. J., & Lieberman, M. D. (2008). Neural bases of moderation of cortisol stress responses by psychosocial resources. Journal of Personality and Social Psychology, 95, 197–211.CrossRefGoogle ScholarPubMed
Taylor, S. E., Repetti, R. L., & Seeman, T. (1997). Health psychology: What is an unhealthy environment and how does it get under the skin? Annual Review of Psychology, 48, 411–447.CrossRefGoogle ScholarPubMed
Tomblingson, G. (2005). Comparison of paired urinary and salivary cortisol measures as biomarkers of stress. Paper presented at the University of Washington's Eighth Annual Undergraduate Research Symposium, Seattle.Google Scholar
Turner, R., & Avison, W. R. (2003). Status variations in stress exposure: Implications for the interpretation of research on race, socioeconomic status, and gender. Journal of Health & Social Behavior, 44, 488–505.CrossRefGoogle ScholarPubMed
Ussher, M., West, R., Evans, P., Steptoe, A., McEwen, A., Clow, A., et al. (2006). Reduction in cortisol after smoking cessation among users of nicotine patches. Psychosomatic Medicine, 68, 299–306.CrossRefGoogle ScholarPubMed
van Eck, M. M., Nicolson, N. A., Berkhof, H., & Sulon, J. (1996). Individual differences in cortisol responses to a laboratory speech task and their relationship to responses to stressful daily events. Biological Psychiatry, 43, 69–84.CrossRefGoogle ScholarPubMed
van Goozen, S. H., Matthys, W., Cohen-Kettenis, P. T., Gispen-de Wied, C., Wiegant, V. M., & van Engeland, H. (1998). Salivary cortisol and cardiovascular activity during stress in oppositional–defiant disorder boys and normal controls. Biological Psychiatry, 43, 531–539.CrossRefGoogle ScholarPubMed
van Honk, J., Schutter, D. J., Hermans, E. J., & Putman, P. (2003). Low cortisol levels and the balance between punishment sensitivity and reward dependency. NeuroReport, 14, 1993–1996.CrossRefGoogle ScholarPubMed
Van Hulle, C. A., Shirtcliff, E. A., Lemery-Chalfant, K., & Goldsmith, H. H. (2011). Genetic and environmental influences on individual differences in cortisol level and circadian rhythm. Manuscript submitted for publication.Google Scholar
Weems, C. F., & Carrion, V. G. (2009). Brief report: Diurnal salivary cortisol in youth—Clarifying the nature of posttraumatic stress dysregulation. Journal of Pediatric Psychology, 34, 389–395.CrossRefGoogle ScholarPubMed
Wilkinson, R. G., & Pickett, K. E. (2009). Income inequality and social dysfunction. Annual Review of Sociology, 35, 493–511.CrossRefGoogle Scholar
Williams, D., & Lawler, K. A. (2001). Stress and illness in low-income women: The roles of hardiness, John Henryism, and race. Women's Health, 32, 61–75.CrossRefGoogle ScholarPubMed
Williams, D. R., & Jackson, P. B. (2005). Social sources of racial disparities in health. Health Affairs, 24, 325–334.CrossRefGoogle ScholarPubMed
Yehuda, R. (2001). Biology of posttraumatic stress disorder. Journal of Clinical Psychiatry, 62(Suppl. 17), 41–46.Google ScholarPubMed
Yehuda, R., Bierer, L. M., Schmeidler, J., Aferiat, D. H., Breslau, I., & Dolan, S. (2000). Low cortisol and risk for PTSD in adult offspring of holocaust survivors. American Journal of Psychiatry, 157, 1252–1259.CrossRefGoogle ScholarPubMed