Fetal programming and gestational diabetes mellitus

被引:74
作者
Monteiro, Lara J. [1 ]
Norman, Jane E. [2 ]
Rice, Gregory E. [3 ]
Illanes, Sebastian E. [1 ,3 ]
机构
[1] Univ Los Andes, Fac Med, Reprod Biol Lab, Dept Obstet & Gynecol, Santiago, Chile
[2] Univ Edinburgh, Queens Med Res Inst, MRC, Tommys Ctr Fetal & Maternal Hlth,Ctr Reprod Hlth, Edinburgh, Midlothian, Scotland
[3] Univ Queensland, Clin Res Ctr, Fac Med & Biomed Sci, Ctr Clin Diagnost, Brisbane, Qld, Australia
关键词
Gestational diabetes mellitus; Fetal programming; Epigenetics; IMPAIRED GLUCOSE-TOLERANCE; BIRTH-WEIGHT; INSULIN-RESISTANCE; EPIGENETIC REGULATION; LONGITUDINAL CHANGES; THRIFTY PHENOTYPE; PRENATAL EXPOSURE; SUBSEQUENT RISK; ADULT HEALTH; LEPTIN GENE;
D O I
10.1016/j.placenta.2015.11.015
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gestational diabetes mellitus is defined by new-onset glucose intolerance during pregnancy. About 2-5% of all pregnant women develop gestational diabetes during their pregnancies and the prevalence has increased considerably during the last decade. This metabolic condition is manifested when pancreatic 13 cells lose their ability to compensate for increased insulin resistance during pregnancy, however, the pathogenesis of the disease remains largely unknown. Gestational diabetes is strongly associated with adverse pregnancy outcome as well as with long-term adverse effects on the offspring which likely occurs due to epigenetic modifications of the fetal genome. In the current review we address gestational diabetes and the short and long term complications for both mothers and offspring focusing on the importance of fetal programming in conferring risk of developing diseases in adulthood. (C) 2015 Published by IFPA and Elsevier Ltd.
引用
收藏
页码:S54 / S60
页数:7
相关论文
共 99 条
[1]  
Aerts L, 1979, J Dev Physiol, V1, P219
[2]   Mendelian randomization supports causality between maternal hyperglycemia and epigenetic regulation of leptin gene in newborns [J].
Allard, C. ;
Desgagne, V. ;
Patenaude, J. ;
Lacroix, M. ;
Guillemette, L. ;
Battista, M. C. ;
Doyon, M. ;
Menard, J. ;
Ardilouze, J. L. ;
Perron, P. ;
Bouchard, L. ;
Hivert, M. F. .
EPIGENETICS, 2015, 10 (04) :342-351
[3]   Treatments for gestational diabetes [J].
Alwan, N. ;
Tuffnell, D. J. ;
West, J. .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2009, (03)
[4]   Sociodemographic Correlates of the Increasing Trend in Prevalence of Gestational Diabetes Mellitus in a Large Population of Women Between 1995 and 2005 [J].
Anna, Vibeke ;
van der Ploeg, Hidde P. ;
Cheung, N. Wah ;
Huxley, Rachel R. ;
Bauman, Adrian E. .
DIABETES CARE, 2008, 31 (12) :2288-2293
[5]  
Association AD, 2004, DIABETES CARE, V27, P2
[6]  
Barker D J, 1992, Paediatr Perinat Epidemiol, V6, P35, DOI 10.1111/j.1365-3016.1992.tb00741.x
[7]   TYPE 2 (NON-INSULIN-DEPENDENT) DIABETES-MELLITUS, HYPERTENSION AND HYPERLIPEMIA (SYNDROME-X) - RELATION TO REDUCED FETAL GROWTH [J].
BARKER, DJP ;
HALES, CN ;
FALL, CHD ;
OSMOND, C ;
PHIPPS, K ;
CLARK, PMS .
DIABETOLOGIA, 1993, 36 (01) :62-67
[8]   Developmental plasticity and human health [J].
Bateson, P ;
Barker, D ;
Clutton-Brock, T ;
Deb, D ;
D'Udine, B ;
Foley, RA ;
Gluckman, P ;
Godfrey, K ;
Kirkwood, T ;
Lahr, MM ;
McNamara, J ;
Metcalfe, NB ;
Monaghan, P ;
Spencer, HG ;
Sultan, SE .
NATURE, 2004, 430 (6998) :419-421
[9]   INCIDENCE AND SEVERITY OF GESTATIONAL DIABETES-MELLITUS ACCORDING TO COUNTRY OF BIRTH IN WOMEN LIVING IN AUSTRALIA [J].
BEISCHER, NA ;
OATS, JN ;
HENRY, OA ;
SHEEDY, MT ;
WALSTAB, JE .
DIABETES, 1991, 40 :35-38
[10]   Metabolic syndrome in childhood: Association with birth weight, maternal obesity, and gestational diabetes mellitus [J].
Boney, CM ;
Verma, A ;
Tucker, R ;
Vohr, BR .
PEDIATRICS, 2005, 115 (03) :E290-E296