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Heritability of metabolic syndrome traits in a large population-based sample

机译:大型人群样本中代谢综合征特征的遗传力

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摘要

Heritability estimates of metabolic syndrome traits vary widely across studies. Some studies have suggested that the contribution of genes may vary with age or sex. We estimated the heritability of 11 metabolic syndrome-related traits and height as a function of age and sex in a large population-based sample of twin families (N = 2,792–27,021, for different traits). A moderate-to-high heritability was found for all traits [from H2 = 0.47 (insulin) to H2 = 0.78 (BMI)]. The broad-sense heritability (H2) showed little variation between age groups in women; it differed somewhat more in men (e.g., for glucose, H2 = 0.61 in young females, H2 = 0.56 in older females, H2 = 0.64 in young males, and H2= 0.27 in older males). While nonadditive genetic effects explained little variation in the younger subjects, nonadditive genetic effects became more important at a greater age. Our findings show that in an unselected sample (age range, ∼18–98 years), the genetic contribution to individual differences in metabolic syndrome traits is moderate to large in both sexes and across age. Although the prevalence of the metabolic syndrome has greatly increased in the past decades due to lifestyle changes, our study indicates that most of the variation in metabolic syndrome traits between individuals is due to genetic differences.
机译:代谢综合征特征的遗传估计在不同研究中差异很大。一些研究表明,基因的贡献可能随年龄或性别而变化。在以人口为基础的双胞胎大样本中,我们估计了11种与代谢综合征相关的性状和身高的遗传力随年龄和性别的变化(N = 2,792–27,021,不同性状)。从所有性状[从H 2 = 0.47(胰岛素)到H 2 = 0.78(BMI)]发现了中等至高的遗传力。广义遗传力(H 2 )显示出女性年龄段之间的差异很小;男性差异更大(例如,葡萄糖,年轻女性的H 2 = 0.61,老年女性的H 2 = 0.56,H 2 = 0.64,在老年男性中H 2 = 0.27)。尽管非加成遗传效应解释了年轻受试者的变异很小,但非加成遗传效应随着年龄的增长而变得越来越重要。我们的发现表明,在未选择的样本中(年龄范围为18-98岁),遗传综合症对代谢综合征特征个体差异的遗传贡献在男女之间以及年龄上均中等至较大。尽管由于生活方式的改变,代谢综合征的患病率在过去几十年中已大大增加,但我们的研究表明,个体之间代谢综合征特征的大部分变化是由于遗传差异造成的。

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