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体重指数变异性的遗传和环境来源:马斯卡廷肥胖家族研究。

The genetic and environmental sources of body mass index variability: the Muscatine Ponderosity Family Study.

作者信息

Moll P P, Burns T L, Lauer R M

机构信息

Department of Epidemiology, University of Michigan, Ann Arbor 48109.

出版信息

Am J Hum Genet. 1991 Dec;49(6):1243-55.

Abstract

The role of genetic and environmental factors in determining the variability in body mass index (BMI; kg/m2) was investigated in 1,302 relatives identified through 284 schoolchildren from Muscatine, IA. BMI levels were first adjusted for variability in age, by gender and by relative type. There was significant familial aggregation of adjusted BMI in the pedigrees, as indicated by inter- and intraclass correlation coefficients significantly different from zero. A mixture of two normal distributions fit the adjusted BMI data better than did a single normal distribution. Genetic and environmental models that could explain both the familial aggregation and the mixture of normal distributions were investigated using complex segregation analysis. There was strong support for a single recessive locus with a major effect that accounted for almost 35% of the adjusted variation in BMI. Polygenic loci accounted for an additional 42% of the variation. Approximately 23% of the adjusted variation was not explained by genetic factors. For spouses living in the same household, their shared environment accounted for 12% of their variation. For siblings living in the same household, their shared environment accounted for 10% of their variation. While shared environments contributed to variation in adjusted BMI, more than 75% of the variation was explained by genetic factors that include a single recessive locus. Approximately 6% of the individuals in the population from which these pedigrees were sampled are predicted to have two copies of the recessive gene, while 37% of the individuals are predicted to have one copy of the gene.

摘要

通过来自爱荷华州马斯卡廷的284名学童识别出1302名亲属,研究了遗传和环境因素在决定体重指数(BMI;千克/平方米)变异性中的作用。首先根据年龄、性别和亲属类型的变异性对BMI水平进行调整。系谱中经调整的BMI存在显著的家族聚集性,组间和组内相关系数均显著不同于零即表明了这一点。两种正态分布的混合比单一正态分布更能拟合经调整的BMI数据。使用复杂分离分析研究了能够解释家族聚集性和正态分布混合情况的遗传和环境模型。有强有力的证据支持一个具有主要效应的单隐性基因座,该基因座占经调整的BMI变异的近35%。多基因座又占变异的42%。约23%的经调整变异无法用遗传因素解释。对于生活在同一家庭的配偶,他们的共同环境占其变异的12%。对于生活在同一家庭的兄弟姐妹,他们的共同环境占其变异的10%。虽然共同环境导致了经调整BMI的变异,但超过75%的变异是由包括一个单隐性基因座在内的遗传因素解释的。预计在抽取这些系谱的人群中,约6%的个体有两个隐性基因拷贝,而37%的个体预计有一个基因拷贝。

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