首页> 外文OA文献 >Evidence that BMI and type 2 diabetes share only a minor fraction of genetic variance: a follow-up study of 23,585 monozygotic and dizygotic twins from the Finnish Twin Cohort Study
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Evidence that BMI and type 2 diabetes share only a minor fraction of genetic variance: a follow-up study of 23,585 monozygotic and dizygotic twins from the Finnish Twin Cohort Study

机译:有证据表明BmI和2型糖尿病只占遗传方差的一小部分:来自芬兰双胞胎队列研究的23,585个同卵双胞胎和双卵双胞胎的后续研究

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摘要

We investigated whether BMI predicts type 2 diabetes in twins and to what extent that is explained by common genetic factors. This was a population-based twin cohort study. Monozygotic (n = 4,076) and dizygotic (n = 9,109) non-diabetic twin pairs born before 1958 answered a questionnaire in 1975, from which BMI was obtained. Information on incident cases of diabetes was obtained by linkage to nationwide registers until 2005. Altogether, 1,332 twins (6.3% of men, 5.1% of women) developed type 2 diabetes. The HR for type 2 diabetes increased monotonically with a mean of 1.22 (95% CI 1.20-1.24) per BMI unit and of 1.97 (95% CI 1.87-2.08) per SD of BMI. The HRs for lean, overweight, obese and morbidly obese participants were 0.59, 2.96, 6.80 and 13.64 as compared with normal weight participants. Model heritability estimates for bivariate variance due to an additive genetic component and non-shared environmental component were 75% (men) and 71% (women) for BMI, and 73% and 64%, respectively for type 2 diabetes. The correlations between genetic variance components (r (g)) indicated that one fifth of the covariance of BMI and type 2 diabetes was due to shared genetic influences. Although the mean monozygotic concordance for type 2 diabetes was approximately twice the dizygotic one, age of onset of diabetes within twin pair members varied greatly, irrespective of zygosity. A 28-year follow-up of adult Finnish twins showed that despite high trait heritability estimates, only a fraction of covariation in BMI and incident type 2 diabetes was of genetic origin.
机译:我们调查了BMI是否可预测双胞胎中的2型糖尿病,以及在何种程度上可以由常见遗传因素解释。这是一项基于人群的双队列研究。 1958年之前出生的单卵双胎(n = 4,076)和双卵双胎(n = 9,109)非糖尿病双胞胎在1975年回答了一个问卷,从中获得了BMI。直到2005年,通过与全国登记册的联系,获得了有关糖尿病事件病例的信息。共有1,332对双胞胎(男性占6.3%,女性占5.1%)发展为2型糖尿病。 2型糖尿病的HR单调增加,每个BMI单位平均为1.22(95%CI 1.20-1.24),每个BMI SD为1.97(95%CI 1.87-2.08)。与正常体重参与者相比,瘦,超重,肥胖和病态肥胖参与者的HR为0.59、2.96、6.80和13.64。对于BMI,由于附加遗传成分和非共有环境成分引起的双变量方差的模型遗传力估计分别为BMI的75%(男性)和71%(女性),以及2型糖尿病的73%和64%。遗传方差成分(r(g))之间的相关性表明,BMI与2型糖尿病的协方差的五分之一是由于共同的遗传影响所致。尽管2型糖尿病的平均单合子一致性约为双合子的两倍,但双胞胎成员中糖尿病的发病年龄差异很大,与合子性无关。对成年芬兰双胞胎进行的28年随访显示,尽管对性状遗传力的估计很高,但BMI和2型糖尿病的协变只有一部分是遗传起源的。

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