EARLY DEVELOPMENTAL CONDITIONING OF LATER HEALTH AND DISEASE: PHYSIOLOGY OR PATHOPHYSIOLOGY?

被引:802
作者
Hanson, M. A.
Gluckman, P. D.
机构
[1] Univ Southampton, Acad Unit Human Dev & Hlth, Southampton, Hants, England
[2] Southampton Univ Hosp, NIHR Nutr Biomed Res Ctr, Southampton, Hants, England
[3] Univ Auckland, Natl Ctr Growth & Dev, Liggins Inst & Gravida, Auckland 1, New Zealand
关键词
LOW-PROTEIN-DIET; LOW-BIRTH-WEIGHT; CARDIOVASCULAR RISK-FACTORS; HIGH-FAT DIET; CORONARY-HEART-DISEASE; FETAL-GROWTH RESTRICTION; SYSTOLIC BLOOD-PRESSURE; PREDICTIVE ADAPTIVE RESPONSES; FOLIC-ACID SUPPLEMENTATION; PKC-EPSILON GENE;
D O I
10.1152/physrev.00029.2013
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Extensive experimental animal studies and epidemiological observations have shown that environmental influences during early development affect the risk of later pathophysiological processes associated with chronic, especially noncommunicable, disease (NCD). This field is recognized as the developmental origins of health and disease (DOHaD). We discuss the extent to which DOHaD represents the result of the physiological processes of developmental plasticity, which may have potential adverse consequences in terms of NCD risk later, or whether it is the manifestation of pathophysiological processes acting in early life but only becoming apparent as disease later. We argue that the evidence suggests the former, through the operation of conditioning processes induced across the normal range of developmental environments, and we summarize current knowledge of the physiological processes involved. The adaptive pathway to later risk accords with current concepts in evolutionary developmental biology, especially those concerning parental effects. Outside the normal range, effects on development can result in nonadaptive processes, and we review their underlying mechanisms and consequences. New concepts concerning the underlying epigenetic and other mechanisms involved in both disruptive and nondisruptive pathways to disease are reviewed, including the evidence for transgenerational passage of risk from both maternal and paternal lines. These concepts have wider implications for understanding the causes and possible prevention of NCDs such as type 2 diabetes and cardiovascular disease, for broader social policy and for the increasing attention paid in public health to the lifecourse approach to NCD prevention.
引用
收藏
页码:1027 / 1076
页数:50
相关论文
共 670 条
[21]   Maternal nutrition, low nephron number, and hypertension in later life: Pathways of nutritional programming [J].
Bagby, Susan P. .
JOURNAL OF NUTRITION, 2007, 137 (04) :1066-1072
[22]   ESSENTIAL-HYPERTENSION PREDICTED BY TRACKING OF ELEVATED BLOOD-PRESSURE FROM CHILDHOOD TO ADULTHOOD - THE BOGALUSA HEART-STUDY [J].
BAO, WH ;
THREEFOOT, SA ;
SRINIVASAN, SR ;
BERENSON, GS .
AMERICAN JOURNAL OF HYPERTENSION, 1995, 8 (07) :657-665
[23]   Human placental growth hormone causes severe insulin resistance in transgenic mice [J].
Barbour, LA ;
Shao, JH ;
Qiao, LP ;
Pulawa, LK ;
Jensen, DR ;
Bartke, A ;
Garrity, M ;
Draznin, B ;
Friedman, JE .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2002, 186 (03) :512-517
[24]   The placental origins of sudden cardiac death [J].
Barker, David J. P. ;
Larsen, Gail ;
Osmond, Clive ;
Thornburg, Kent L. ;
Kajantie, Eero ;
Eriksson, Johan G. .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2012, 41 (05) :1394-1399
[25]  
BARKER DJP, 1989, LANCET, V2, P577
[26]   THE FETAL AND INFANT ORIGINS OF ADULT DISEASE [J].
BARKER, DJP .
BRITISH MEDICAL JOURNAL, 1990, 301 (6761) :1111-1111
[27]   GROWTH INUTERO, BLOOD-PRESSURE IN CHILDHOOD AND ADULT LIFE, AND MORTALITY FROM CARDIOVASCULAR-DISEASE [J].
BARKER, DJP ;
OSMOND, C ;
GOLDING, J ;
KUH, D ;
WADSWORTH, MEJ .
BRITISH MEDICAL JOURNAL, 1989, 298 (6673) :564-567
[28]   FETAL ORIGINS OF CORONARY HEART-DISEASE [J].
BARKER, DJP .
BRITISH MEDICAL JOURNAL, 1995, 311 (6998) :171-174
[29]  
BARKER DJP, 1986, LANCET, V1, P1077
[30]  
BASSETT NS, 1990, J DEV PHYSIOL, V14, P73