4.6 Review

Child Health, Developmental Plasticity, and Epigenetic Programming

Journal

ENDOCRINE REVIEWS
Volume 32, Issue 2, Pages 159-224

Publisher

ENDOCRINE SOC
DOI: 10.1210/er.2009-0039

Keywords

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Funding

  1. Vaxthuset Foundation for Children
  2. European Society for Pediatric Endocrinology
  3. Pfizer Endocrine Care
  4. Agence National de la Recherche
  5. Institut National du Cancer
  6. Association for International Cancer Research
  7. INSERM
  8. Universite Pierre et Marie Curie-Paris 6 (UPMC)
  9. French Research Agency (ANR)
  10. French National Ministry of Health (PHRC)
  11. Biomedecine Agency
  12. United States National Institutes of Health
  13. New Zealand government
  14. Biotechnology and Biological Sciences Research Council [BB/D01235X/2, BB/D01235X/1] Funding Source: researchfish
  15. Medical Research Council [MC_U106179472, G0600717B] Funding Source: researchfish
  16. BBSRC [BB/D01235X/2, BB/D01235X/1] Funding Source: UKRI
  17. MRC [MC_U106179472] Funding Source: UKRI

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Plasticity in developmental programming has evolved in order to provide the best chances of survival and reproductive success to the organism under changing environments. Environmental conditions that are experienced in early life can profoundly influence human biology and long-term health. Developmental origins of health and disease and life-history transitions are purported to use placental, nutritional, and endocrine cues for setting long-term biological, mental, and behavioral strategies in response to local ecological and/or social conditions. The window of developmental plasticity extends from preconception to early childhood and involves epigenetic responses to environmental changes, which exert their effects during life-history phase transitions. These epigenetic responses influence development, cell-and tissue-specific gene expression, and sexual dimorphism, and, in exceptional cases, could be transmitted transgenerationally. Translational epigenetic research in child health is areiterative process that ranges from research in the basic sciences, preclinical research, and pediatric clinical research. Identifying the epigenetic consequences of fetal programming creates potential applications in clinical practice: the development of epigenetic biomarkers for early diagnosis of disease, the ability to identify susceptible individuals at risk for adult diseases, and the development of novel preventive and curative measures that are based on diet and/or novel epigenetic drugs. (Endocrine Reviews 32: 159-224, 2011)

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