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Co-regulation of stress in uterus and during early infancy mediates early programming of gender differences in attachment styles: Evolutionary, genetic, and endocrinal perspectives

Published online by Cambridge University Press:  12 February 2009

Sari Goldstein Ferber
Sari Goldstein Ferber
Affiliation:
Division of Developmental Neuroscience, New York State Psychiatric Institute and Department of Psychiatry, Columbia University, New York, NY 10032; Department of Neonatology, Wolfson Medical Center, Sackler School of Medicine, and Department of Neurobiochemistry, Tel Aviv University, Tel Aviv 58100, Israel. sg2694@columbia.edu
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Abstract

According to evolutionary, genetic, and endocrinal perspectives, gender differences are modulated by the interaction between intra-uterine stress, genetic equipments, and the availability of the facilitating environment during the newborn period. The social message of fitness over obstacles during socialization and the discussion of secure/non-secure attachment styles should take into consideration the brain functions, which are altered differently in response to intra- and extra-uterine stress in each gender.

Type
Open Peer Commentary
Information
Behavioral and Brain Sciences , Volume 32 , Issue 1 , February 2009 , pp. 29 - 30
Copyright
Copyright © Cambridge University Press 2009

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References

Als, H. (1986) A synactive model of neonatal behavioral organization: Framework for assessment of neurobehavioral development in the premature infant and for support of infants and parents in the neonatal intensive care environment. Physical and Occupational Therapy in Pediatrics 6(Special issue):3–55.CrossRefGoogle Scholar
Als, H., Duffy, F. H., McAnulty, G. B., Rivkin, M. J., Vajapeyam, S., Mulkern, R. V., Warfield, S. K., Huppi, P. S., Butler, S. C., Conneman, N., Fischer, C. & Eichenwald, E. C. (2004) Early experience alters brain function and structure. Pediatrics 113(4):846–57.Google Scholar
Als, H., Lawhon, G., Duffy, F. H., McAnulty, G. B., Gibes-Grossman, R. & Blickman, J. G. (1994) Individualized developmental care for the very low-birth-weight preterm infant: Medical and neurofunctional effects. Journal of the American Medical Association (JAMA) 272(11):853–58.CrossRefGoogle ScholarPubMed
Anderson, P. J. & Doyle, L. W. (2008) Cognitive and educational deficits in children born extremely preterm. Seminars in Perinatology 32:51–58.Google Scholar
Archer, J. (1996) Sex differences in social behavior – Are the social role and evolutionary explanations compatible? American Psychologist 51(9):909–17.CrossRefGoogle ScholarPubMed
Cellerino, A. & Jannini, E. A. (2005) Male reproductive physiology as a sexually selected handicap? Erectile dysfunction is correlated with general health and health prognosis and may have evolved as a marker of poor phenotypic quality. Medical Hypotheses 65:179–84.CrossRefGoogle ScholarPubMed
Cho, J., Holditch-Davis, D. & Belyea, M. (2007) Gender and racial differences in the looking and talking behaviors of mothers and their 3-year-old prematurely born children. Journal of Pediatric Nursing 22(5):356–67.Google Scholar
Davis, M. & Emory, E. (1995) Sex differences in neonatal stress reactivity. Child Development 66:14–27.Google Scholar
Deulofeut, R., Dudell, G. & Sola, A. (2007) Treatment-by-gender effect when aiming to avoid hyperoxia in preterm infants in the NICU. Acta Paediatrica 96:990–94.Google Scholar
Francis, D. D., Young, L. J., Meaney, M. J. & Insel, T. R. (2002) Naturally occurring differences in maternal care are associated with the expression of oxytocin and vasopressin (V1a) receptors: Gender differences. Journal of Neuroendocrinology 14:349–53.CrossRefGoogle ScholarPubMed
Goldstein Ferber, S. (2008) The concept of co-regulation between neurobehavioral sub-systems: The logic interplay between excitatory and inhibitory ends. Behavioral and Brain Sciences 31(3):337–38.CrossRefGoogle Scholar
Heckmann, M., Hartmann, F. M., Kampschulte, B., Gack, H., Bodeker, R. H., Gorther, L. & Wudy, S. A. (2005) Cortisol production rates in preterm infants in relation to growth and illness: A noninvasive prospective study using gas chromatography-mass spectrometry. Journal of Clinical Endocrinology and Metabolism 90(10):5737–42.CrossRefGoogle ScholarPubMed
Hofer, M. A. (1994) Early relationships as regulators of infant physiology and behavior. Acta Paediatrica (Suppl.) 397:9–18.CrossRefGoogle ScholarPubMed
Huber, D., Veinante, P. & Stoop, R. (2005) Vasopressinand oxytocin excite distinct neuronal populations in the central amygdala. Science 308:245–48.CrossRefGoogle Scholar
Ingemarsson, I. (2003) Gender aspects of preterm birth. British Journal of Obstetrics and Gynaecology 110(20):34–38.CrossRefGoogle ScholarPubMed
Jones, H. P., Karuri, S., Cronin, C. M. G., Ohlsson, A., Peliowski, A., Synnes, A., Lee, S. K. & the Canadian Neonatal Network (2005) Actuarial survival of a large Canadian cohort of preterm infants. BMC Pediatrics 5:40.Google Scholar
Meaney, M. J. & Szyf, M. (2005) Environmental programming of stress responses through DNA methylation: Life at the interface between a dynamic environment and a fixed genome. Dialogues in Clinical NeuroSciences 7(2):103–23.CrossRefGoogle Scholar
Phillips, D. I. W. (2007) Programming of the stress response: A fundamental mechanism underlying the long-term effects of fetal environment? Journal of Internal Medicine 261:453–60.CrossRefGoogle ScholarPubMed
Pressler, J. L. & Hepworth, J. T. (2002) A quantitative use of the NIDCAP tool: The effect of gender and race on very preterm neonate's behavior. Clinical Nursing Research 11(1):89–102.Google ScholarPubMed