Epigenetic epidemiology of the developmental origins hypothesis

被引:574
作者
Waterland, Robert A. [1 ]
Michels, Karin B.
机构
[1] Baylor Coll Med, Dept Pediat, USDA Childrens Nutr Res Ctr, Houston, TX 77030 USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Obstet & Gynecol Epidemiol Ctr,Dept Obstet Gyneco, Boston, MA 02115 USA
关键词
chromatin; DNA methylation; epigenomics; metabolic imprinting; nutrition;
D O I
10.1146/annurev.nutr.27.061406.093705
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Extensive human epidemiologic and animal model data indicate that during critical periods of prenatal and postnatal mammalian development, nutrition and other environmental stimuli influence developmental pathways and thereby induce permanent changes in metabolism and chronic disease susceptibility. The biologic mechanisms underlying this "developmental origins hypothesis" are poorly understood. This review focuses on the likely involvement of epigenetic mechanisms in the developmental origins of health and disease (DOHaD). We describe permanent effects of transient environmental influences on the developmental establishment of epigenetic gene regulation and evidence linking epigenetic dysregulation with human disease. We propose a definition of "epigenetic epidemiology" and delineate how this emerging field provides a basis from which to explore the role of epigenetic mechanisms in DOHaD. We suggest strategies for future human epidemiologic studies to identify causal associations between early exposures, long-term changes in epigenetic regulation, and disease, which may ultimately enable specific early-life interventions to improve human health.
引用
收藏
页码:363 / 388
页数:26
相关论文
共 135 条
[1]   FETAL ORIGINS OF CORONARY HEART-DISEASE [J].
BARKER, DJP .
BRITISH MEDICAL JOURNAL, 1995, 311 (6998) :171-174
[2]   GROWTH IN-UTERO AND SERUM-CHOLESTEROL CONCENTRATIONS IN ADULT LIFE [J].
BARKER, DJP ;
MARTYN, CN ;
OSMOND, C ;
HALES, CN ;
FALL, CHD .
BRITISH MEDICAL JOURNAL, 1993, 307 (6918) :1524-1527
[3]  
BARKER DJP, 1986, LANCET, V1, P1077
[4]  
Belshaw NJ, 2004, CANCER EPIDEM BIOMAR, V13, P1495
[5]   RNA meets chromatin [J].
Bernstein, E ;
Allis, CD .
GENES & DEVELOPMENT, 2005, 19 (14) :1635-1655
[6]   DNA methylation patterns and epigenetic memory [J].
Bird, A .
GENES & DEVELOPMENT, 2002, 16 (01) :6-21
[7]   An integrated epigenetic and genetic approach to common human disease [J].
Bjornsson, HT ;
Fallin, MD ;
Feinberg, AP .
TRENDS IN GENETICS, 2004, 20 (08) :350-358
[8]   Trophic action of leptin on hypothalamic neurons that regulate feeding [J].
Bouret, SG ;
Draper, SJ ;
Simerly, RB .
SCIENCE, 2004, 304 (5667) :108-110
[9]   SP1 ELEMENTS PROTECT A CPG ISLAND FROM DE-NOVO METHYLATION [J].
BRANDEIS, M ;
FRANK, D ;
KESHET, I ;
SIEGFRIED, Z ;
MENDELSOHN, M ;
NEMES, A ;
TEMPER, V ;
RAZIN, A ;
CEDAR, H .
NATURE, 1994, 371 (6496) :435-438
[10]   Homocysteine metabolism, hyperhomocysteinaemia and vascular disease: An overview [J].
Castro, R ;
Rivera, I ;
Blom, HJ ;
Jakobs, C ;
de Almeida, IT .
JOURNAL OF INHERITED METABOLIC DISEASE, 2006, 29 (01) :3-20