The developmental origins of adult disease

被引:1075
作者
Barker, DJP [1 ]
机构
[1] Univ Southampton, Southampton Gen Hosp, MRC Epidemiol Ctr, Southampton SO16 6YD, Hants, England
关键词
maternal diet; developmental origins of disease; or developmental origins; cardiovascular disease; low birthweight;
D O I
10.1080/07315724.2004.10719428
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
Low birthweight is now known to be associated with increased rates of coronary heart disease and the related disorders stroke, hypertension and non-insulin dependent diabetes. These associations have been extensively replicated in studies in different countries and are not the result of confounding variables. They extend across the normal range of birthweight and depend on lower birthweights in relation to the duration of gestation rather than the effects of premature birth. The associations are thought to be consequences of developmental plasticity, the phenomenon by which one genotype can give rise to a range of different physiological or morphological states in response to different environmental conditions during development. Recent observations have shown that impaired growth in infancy and rapid childhood weight gain exacerbate the effects of impaired prenatal growth. A new vision of optimal early human development is emerging which takes account of both short and long-term outcomes.
引用
收藏
页码:588S / 595S
页数:8
相关论文
共 45 条
[11]   Early growth and coronary heart disease in later life:: longitudinal study [J].
Eriksson, JG ;
Forsén, T ;
Tuomilehto, J ;
Osmond, C ;
Barker, DJP .
BRITISH MEDICAL JOURNAL, 2001, 322 (7292) :949-953
[12]   Early adiposity rebound in childhood and risk of Type 2 diabetes in adult life [J].
Eriksson, JG ;
Forsén, T ;
Tuomilehto, J ;
Osmond, C ;
Barker, DJP .
DIABETOLOGIA, 2003, 46 (02) :190-194
[13]   The effects of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor-γ2 gene on insulin sensitivity and insulin metabolism interact with size at birth [J].
Eriksson, JG ;
Lindi, V ;
Uusitupa, M ;
Forsén, TJ ;
Laakso, M ;
Osmond, C ;
Barker, DJP .
DIABETES, 2002, 51 (07) :2321-2324
[14]   Effects of size at birth and childhood growth on the insulin resistance syndrome in elderly individuals [J].
Eriksson, JG ;
Forsén, T ;
Tuomilehto, J ;
Jaddoe, VWV ;
Osmond, C ;
Barker, DJP .
DIABETOLOGIA, 2002, 45 (03) :342-348
[15]   Growth in utero and during childhood among women who develop coronary heart disease:: longitudinal study [J].
Forsén, T ;
Eriksson, JG ;
Tuomilehto, J ;
Osmond, C ;
Barker, DJP .
BRITISH MEDICAL JOURNAL, 1999, 319 (7222) :1403-1407
[16]   Growth of girls who later develop coronary heart disease [J].
Forsén, T ;
Osmond, C ;
Eriksson, JG ;
Barker, DJP .
HEART, 2004, 90 (01) :20-24
[17]   Mother's weight in pregnancy and coronary heart disease in a cohort of Finnish men: Follow up study [J].
Forsen, T ;
Eriksson, JG ;
Tuomilehto, J ;
Teramo, K ;
Osmond, C ;
Barker, DJP .
BRITISH MEDICAL JOURNAL, 1997, 315 (7112) :837-840
[18]   The fetal and childhood growth of persons who develop type 2 diabetes [J].
Forsén, T ;
Eriksson, J ;
Tuomilehto, J ;
Reunanen, A ;
Osmond, C ;
Barker, D .
ANNALS OF INTERNAL MEDICINE, 2000, 133 (03) :176-182
[19]   Birthweight, body-mass index in middle age, and incident coronary heart disease [J].
Frankel, S ;
Elwood, P ;
Sweetnam, P ;
Yarnell, J ;
Smith, GD .
LANCET, 1996, 348 (9040) :1478-1480
[20]   FETAL AND INFANT GROWTH AND IMPAIRED GLUCOSE-TOLERANCE AT AGE 64 [J].
HALES, CN ;
BARKER, DJP ;
CLARK, PMS ;
COX, LJ ;
FALL, C ;
OSMOND, C ;
WINTER, PD .
BMJ-BRITISH MEDICAL JOURNAL, 1991, 303 (6809) :1019-1022