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首页> 外文期刊>Proceedings of the Nutrition Society >Interactions of perturbations in intrauterine growth and growth duringchildhood on the risk of adult-onset disease
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Interactions of perturbations in intrauterine growth and growth duringchildhood on the risk of adult-onset disease

机译:宫内生长扰动和儿童期生长对成年发病风险的相互作用

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摘要

The 'fetal origins' hypothesis (Barker, 1995) would predict that the rising epidemic of diabetes and CHD in India would be due to poor intrauterine growth of the Indian babies. While this explanation may be valid to an extent, the higher prevalence of these disorders in urban compared with rural India (where birth weights are lower) would suggest a significant role for postnatal factors. In a cohort of 477 children born in the King Edward Memorial Hospital, Pune, we found that at 8 years of age current obesity strongly predicted insulin resistance. When this effect was allowed for, low birth weight was significantly associated with insulin-resistance variables and other cardiovascular risk factors. Children who were born small but had grown heavy (or tall) were the most insulin resistant and had the highest levels of cardiovascular risk factors. Accelerated growth in relation to mid parental height was similarly predictive. Poor intrauterine growth also predicted higher central adiposity at 8 years of age. We have also studied maternal nutrition and fetal growth in six villages near Pune. A newborn Indian baby is small (2650 g, SD score (SDS) - 1.6 compared with an average white Caucasian baby born in the UK) and 'thin' (ponderal index 2.45 kg/m(3), SDS -1.2), but has preserved its subcutaneous fat (subscapular skinfold thickness SDS -0.6). The thinness of the Indian babies is due to poor muscle and small abdominal viscera. We have proposed this composition as the 'thrifty phenotype' (Hales & Barker, 1992) of Indian babies. Maternal size and intake of certain food groups during pregnancy were important determinants of the baby's phenotype. Thus, the small Indian babies are programmed to deposit fat from their intrauterine life. Exaggeration of this tendency in later life is associated with insulin-resistance syndrome. Control of the insulin-resistance epidemic in India might depend on improved intrauterine development and prevention of childhood obesity.
机译:“胎儿起源”假说(Barker,1995)将预测印度糖尿病和冠心病的流行正在上升,这是由于印度婴儿的子宫内生长不良所致。尽管这种解释在一定程度上可能是正确的,但与印度农村地区(出生体重较低)相比,这些疾病在城市中的患病率更高,这表明出生后因素起着重要作用。在浦那国王爱德华纪念医院出生的477名儿童中,我们发现8岁时的肥胖强烈预测了胰岛素抵抗。当允许这种效果时,低出生体重与胰岛素抵抗变量和其他心血管危险因素显着相关。出生时小但长大(或长大)的孩子对胰岛素的抵抗力最高,并且具有最高的心血管危险因素水平。与父母中段身高相关的加速生长也具有类似的预测作用。子宫内生长不良也预示着8岁时较高的中央肥胖。我们还研究了浦那附近六个村庄的孕产妇营养和胎儿生长情况。印度新生婴儿很小(2650 g,SD评分(SDS)-与英国出生的白人白种人婴儿的平均水平相比为1.6)和“瘦”(肾指数2.45 kg / m(3),SDS -1.2),但保留了皮下脂肪(肩cap下皮褶厚度SDS -0.6)。印度婴儿的瘦弱是由于肌肉不良和腹部内脏小。我们提出了这种成分作为印度婴儿的“节俭表型”(Hales&Barker,1992)。孕妇在怀孕期间某些食物种类的大小和摄入量是婴儿表型的重要决定因素。因此,印度小婴儿被编程为从子宫内生活中沉积脂肪。在以后的生活中这种趋势的夸大与胰岛素抵抗综合征有关。在印度,控制胰岛素抵抗的流行可能取决于宫内发育的改善和儿童肥胖的预防。

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