Insulin resistance syndrome in 8-year-old Indian children - Small at birth, big at 8 years, or both?

被引:446
作者
Bavdekar, A
Yajnik, CS [1 ]
Fall, CHD
Bapat, S
Pandit, AN
Deshpande, V
Bhave, S
Kellingray, SD
Joglekar, C
机构
[1] King Edward Mem Hosp, Diabet Unit, Pune 411011, Maharashtra, India
[2] King Edward Mem Hosp, Dept Pediat, Pune 411011, Maharashtra, India
[3] Univ Southampton, MRC, Environm Epidemiol Unit, Southampton Gen Hosp, Southampton, Hants, England
基金
英国惠康基金;
关键词
D O I
10.2337/diabetes.48.12.2422
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have studied 477 8-year-old Indian children to define the relationship between birth weight and cardiovascular risk factors, including insulin resistance syndrome (IRS) variables and plasma total and LDL cholesterol concentrations. All risk factors were strongly related to current weight. After adjustment for current weight, age, and sex, lower birth weight was associated with higher systolic blood pressure (P = 0.008), fasting plasma insulin and 32-33 split proinsulin concentrations (P = 0.08 and 0.02), glucose and insulin concentrations 30 min postglucose (P = 0.06 and 0.04), subscapular/triceps skinfold ratio (P = 0.003), and plasma total and LDL cholesterol concentrations (P = 0.002 and 0.001). Lower birth weight was associated with increased calculated insulin resistance (homeostasis model assessment [HOMA], P = 0.03), but was not related to the HOMA index of beta-cell function. The highest levels of IRS variables and total and LDL cholesterol were in children of low birth weight but high fat mass at 8 years. Taller height at 8 years predicted higher fasting plasma insulin concentrations, insulin resistance, and plasma total and LDL cholesterol concentrations. The most insulin-resistant children were those who had short parents but had themselves grown tall. Although the implications of our findings in relation to height are unclear, interventions to improve fetal growth and to control obesity in childhood are likely to be important factors in the prevention of cardiovascular disease and IRS in India.
引用
收藏
页码:2422 / 2429
页数:8
相关论文
共 57 条
[21]  
Gupta R, 1996, Indian Heart J, V48, P241
[22]   TYPE-2 (ON-INSULIN-DEPENDENT) DIABETES-MELLITUS - THE THRIFTY PHENOTYPE HYPOTHESIS [J].
HALES, CN ;
BARKER, DJP .
DIABETOLOGIA, 1992, 35 (07) :595-601
[23]   Mutations in the glucokinase gene of the fetus result in reduced birth weight [J].
Hattersley, AT ;
Beards, F ;
Ballantyne, E ;
Appleton, M ;
Harvey, R ;
Ellard, S .
NATURE GENETICS, 1998, 19 (03) :268-270
[24]   The fetal insulin hypothesis: an alternative explanation of the association of low birthweight with diabetes and vascular disease [J].
Hattersley, AT ;
Tooke, JE .
LANCET, 1999, 353 (9166) :1789-1792
[25]   TUMOR-NECROSIS-FACTOR-ALPHA - A KEY COMPONENT OF THE OBESITY-DIABETES LINK [J].
HOTAMISLIGIL, GS ;
SPIEGELMAN, BM .
DIABETES, 1994, 43 (11) :1271-1278
[26]  
KRAMER MS, 1987, B WORLD HEALTH ORGAN, V65, P663
[27]  
KUPPUSWAMY B, 1962, MANUAL SOCIOECONOMIC
[28]   EARLY GROWTH AND ABDOMINAL FATNESS IN ADULT LIFE [J].
LAW, CM ;
BARKER, DJP ;
OSMOND, C ;
FALL, CHD ;
SIMMONDS, SJ .
JOURNAL OF EPIDEMIOLOGY AND COMMUNITY HEALTH, 1992, 46 (03) :184-186
[29]   INITIATION OF HYPERTENSION INUTERO AND ITS AMPLIFICATION THROUGHOUT LIFE [J].
LAW, CM ;
DESWIET, M ;
OSMOND, C ;
FAYERS, PM ;
BARKER, DJP ;
CRUDDAS, AM ;
FALL, CHD .
BRITISH MEDICAL JOURNAL, 1993, 306 (6869) :24-27
[30]  
Leon DA, 1996, BRIT MED J, V312, P401, DOI 10.1136/bmj.312.7028.401