The thrifty phenotype hypothesis

被引:1780
作者
Hales, CN
Barker, DJP
机构
[1] Univ Cambridge, Addenbrookes Hosp, Dept Clin Biochem, Cambridge CB2 2QR, England
[2] Southampton Gen Hosp, MRC, Environm Epidemiol Unit, Southampton, Hants, England
关键词
D O I
10.1093/bmb/60.1.5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The thrifty phenotype hypothesis proposes that the epidemiological associations between poor fetal and infant growth and the subsequent development of type 2 diabetes and the metabolic syndrome result from the effects of poor nutrition in early life, which produces permanent changes in glucose-insulin metabolism. These changes include reduced capacity for insulin secretion and insulin resistance which, combined with effects of obesity, ageing and physical inactivity, are the most important factors in determining type 2 diabetes. Since the hypothesis was proposed, many studies world-wide have confirmed the initial epidemiological evidence, although the strength of the relationships has varied from one study to another. The relationship with insulin resistance is clear at all ages studied. Less clear is the relationship with insulin secretion. The relative contribution of genes and environment to these relationships remains a matter of debate. The contributions of maternal hyperglycaemia and the trajectory of postnatal growth need to be clarified.
引用
收藏
页码:5 / 20
页数:16
相关论文
共 47 条
[31]   Effects of infant birthweight and maternal body mass index in pregnancy on components of the insulin resistance syndrome in China [J].
Mi, J ;
Law, C ;
Zhang, KL ;
Osmond, C ;
Stein, C ;
Barker, D .
ANNALS OF INTERNAL MEDICINE, 2000, 132 (04) :253-+
[32]  
Olah K. S., 1996, Journal of Obstetrics and Gynaecology (Abingdon), V16, P5, DOI 10.3109/01443619609028371
[33]   The insulin gene VNTR, type 2 diabetes and birth weight [J].
Ong, KKL ;
Phillips, DI ;
Fall, C ;
Poulton, J ;
Bennett, ST ;
Golding, J ;
Todd, JA ;
Dunger, DB .
NATURE GENETICS, 1999, 21 (03) :262-263
[34]   THINNESS AT BIRTH AND INSULIN-RESISTANCE IN ADULT LIFE [J].
PHILLIPS, DIW ;
BARKER, DJP ;
HALES, CN ;
HIRST, S ;
OSMOND, C .
DIABETOLOGIA, 1994, 37 (02) :150-154
[35]   FETAL GROWTH AND IMPAIRED GLUCOSE-TOLERANCE IN MEN AND WOMEN [J].
PHIPPS, K ;
BARKER, DJP ;
HALES, CN ;
FALL, CHD ;
OSMOND, C ;
CLARK, PMS .
DIABETOLOGIA, 1993, 36 (03) :225-228
[36]   Heritability of Type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance - a population-based twin study [J].
Poulsen, P ;
Kyvik, KO ;
Vaag, A ;
Beck-Nielsen, H .
DIABETOLOGIA, 1999, 42 (02) :139-145
[37]   Low birth weight is associated with NIDDM in discordant monozygotic and dizygotic twin pairs [J].
Poulsen, P ;
Vaag, AA ;
Kyvik, KO ;
Jensen, DM ;
BeckNielsen, H .
DIABETOLOGIA, 1997, 40 (04) :439-446
[38]   Glucose tolerance in adults after prenatal exposure to famine [J].
Ravelli, ACJ ;
van der Meulen, JHP ;
Michels, RPJ ;
Osmond, C ;
Barker, DJP ;
Hales, CN ;
Bleker, OP .
LANCET, 1998, 351 (9097) :173-177
[39]   Birthweight and the risk for type 2 diabetes mellitus in adult women [J].
Rich-Edwards, JW ;
Colditz, GA ;
Stampfer, MJ ;
Willett, WC ;
Gillman, MW ;
Hennekens, CH ;
Speizer, FE ;
Manson, JE .
ANNALS OF INTERNAL MEDICINE, 1999, 130 (04) :278-+
[40]   THE RELATION OF FETAL GROWTH TO PLASMA-GLUCOSE IN YOUNG MEN [J].
ROBINSON, S ;
WALTON, RJ ;
CLARK, PM ;
BARKER, DJP ;
HALES, CN ;
OSMOND, C .
DIABETOLOGIA, 1992, 35 (05) :444-446