TY - JOUR
T1 - Incorporating epigenetic mechanisms to advance fetal programming theories
AU - Conradt, Elisabeth
AU - Adkins, Daniel E.
AU - Crowell, Sheila E.
AU - Raby, K. Lee
AU - Diamond, Lisa M.
AU - Ellis, Bruce
N1 - Funding Information:
The first author (E.C.) and the senior author (B.E.) contributed equally to this manuscript. This manuscript was supported by the National Institute of Mental Health under Award Number R21MH109777 (to S.C. and E.C.), a Career Development Award from the National Institute on Drug Abuse 7K08DA038959-02 (to E.C.), and a grant from the University of Utah Consortium for Families and Health Research. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute of Mental Health, the National Institute on Drug Abuse, or the National Institutes of Health.
Publisher Copyright:
© Copyright 2018 Cambridge University Press.
PY - 2018/8/1
Y1 - 2018/8/1
N2 - Decades of fetal programming research indicates that we may be able to map the origins of many physical, psychological, and medical variations and morbidities before the birth of the child. While great strides have been made in identifying associations between prenatal insults, such as undernutrition or psychosocial stress, and negative developmental outcomes, far less is known about how adaptive responses to adversity regulate the developing phenotype to match stressful conditions. As the application of epigenetic methods to human behavior has exploded in the last decade, research has begun to shed light on the role of epigenetic mechanisms in explaining how prenatal conditions shape later susceptibilities to mental and physical health problems. In this review, we describe and attempt to integrate two dominant fetal programming models: the cumulative stress model (a disease-focused approach) and the match-mismatch model (an evolutionary-developmental approach). In conjunction with biological sensitivity to context theory, we employ these two models to generate new hypotheses regarding epigenetic mechanisms through which prenatal and postnatal experiences program child stress reactivity and, in turn, promote development of adaptive versus maladaptive phenotypic outcomes. We conclude by outlining priority questions and future directions for the fetal programming field.
AB - Decades of fetal programming research indicates that we may be able to map the origins of many physical, psychological, and medical variations and morbidities before the birth of the child. While great strides have been made in identifying associations between prenatal insults, such as undernutrition or psychosocial stress, and negative developmental outcomes, far less is known about how adaptive responses to adversity regulate the developing phenotype to match stressful conditions. As the application of epigenetic methods to human behavior has exploded in the last decade, research has begun to shed light on the role of epigenetic mechanisms in explaining how prenatal conditions shape later susceptibilities to mental and physical health problems. In this review, we describe and attempt to integrate two dominant fetal programming models: the cumulative stress model (a disease-focused approach) and the match-mismatch model (an evolutionary-developmental approach). In conjunction with biological sensitivity to context theory, we employ these two models to generate new hypotheses regarding epigenetic mechanisms through which prenatal and postnatal experiences program child stress reactivity and, in turn, promote development of adaptive versus maladaptive phenotypic outcomes. We conclude by outlining priority questions and future directions for the fetal programming field.
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U2 - 10.1017/S0954579418000469
DO - 10.1017/S0954579418000469
M3 - Article
C2 - 30068415
AN - SCOPUS:85051030076
SN - 0954-5794
VL - 30
SP - 807
EP - 824
JO - Development and Psychopathology
JF - Development and Psychopathology
IS - 3
ER -