Developmental origins of diabetes-an Indian perspective

被引:22
作者
Krishnaveni, G. V. [1 ]
Yajnik, C. S. [2 ]
机构
[1] CSI Holdsworth Mem Hosp, Epidemiol Res Unit, Mysore 570021, Karnataka, India
[2] King Edward Mem Hosp & Res Ctr, Diabet Unit, Pune, Maharashtra, India
关键词
PUNE MATERNAL NUTRITION; BODY-MASS INDEX; INSULIN-RESISTANCE; BIRTH-WEIGHT; CARDIOVASCULAR RISK; GLUCOSE-TOLERANCE; FETAL-GROWTH; NEONATAL ANTHROPOMETRY; FOLATE CONCENTRATIONS; METABOLIC SYNDROME;
D O I
10.1038/ejcn.2017.87
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
The developmental origins of health disease (DOHaD) hypothesis proposes that altered environmental influences (nutrition, metabolism, pollutants, stress and so on) during critical stages of fetal growth predisposes individuals to diabetes and other non-communicable disease in later life. This phenomenon is thought to reflect permanent effects ('programming') of unbalanced fetal development on physiological systems. Intrauterine programming may underlie the characteristic Indian 'thin-fat' phenotype and the current unprecedented epidemic of diabetes on the backdrop of multigenerational maternal undernutrition in the country. India has been at the forefront of the DOHaD research for over two decades. Both retrospective and prospective birth cohorts in India provide evidence for the role of impaired early-life nutrition on the later diabetes risk. These studies show that in a transitioning country such as India, maternal undernutrition (of micronutrients) and overnutrition (gestational diabetes) co-exist, and expose the offspring to disease risk through multiple pathways. Currently, the Indian scientists are embarking on complex mechanistic and intervention studies to find solutions for the diabetes susceptibility of this population. However, a few unresolved issues in this context warrant continued research and a cautious approach.
引用
收藏
页码:865 / 869
页数:5
相关论文
共 45 条
[1]   Body composition, visceral fat, leptin, and insulin resistance in Asian Indian men [J].
Banerji, MA ;
Faridi, N ;
Atluri, R ;
Chaiken, RL ;
Lebovitz, HE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (01) :137-144
[2]   Resource allocation in utero and health in later life [J].
Barker, D. J. P. ;
Lampl, M. ;
Roseboom, T. ;
Winder, N. .
PLACENTA, 2012, 33 :E30-E34
[3]  
Barker D. J. P., 1998, MOTHERS BABIES HLTH
[4]   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
[5]   Insulin resistance syndrome in 8-year-old Indian children - Small at birth, big at 8 years, or both? [J].
Bavdekar, A ;
Yajnik, CS ;
Fall, CHD ;
Bapat, S ;
Pandit, AN ;
Deshpande, V ;
Bhave, S ;
Kellingray, SD ;
Joglekar, C .
DIABETES, 1999, 48 (12) :2422-2429
[6]   Relation of serial changes in childhood body-mass index to impaired glucose tolerance in young adulthood [J].
Bhargava, SK ;
Sachdev, HS ;
Fall, CHD ;
Osmond, C ;
Lakshmy, R ;
Barker, DJP ;
Biswas, SKD ;
Ramji, S ;
Prabhakaran, D ;
Reddy, KS .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (09) :865-875
[7]   Relationship between generalized and upper body obesity to insulin resistance in Asian Indian men [J].
Chandalia, M ;
Abate, N ;
Garg, A ;
Stray-Gundersen, J ;
Grundy, SM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (07) :2329-2335
[8]  
Fall CHD, 1998, DIABETIC MED, V15, P220, DOI 10.1002/(SICI)1096-9136(199803)15:3<220::AID-DIA544>3.3.CO
[9]  
2-F
[10]   OF PREGNANCY AND PROGENY [J].
FREINKEL, N .
DIABETES, 1980, 29 (12) :1023-1035