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曼哈顿北部家庭研究中代谢综合征及其组成部分的遗传度

Heritabilities of the metabolic syndrome and its components in the Northern Manhattan Family Study.

作者信息

Lin H-F, Boden-Albala B, Juo S H, Park N, Rundek T, Sacco R L

机构信息

Genome Center, Columbia University, 1150 Saint Nicholas Avenue, New York, NY 10032, USA.

出版信息

Diabetologia. 2005 Oct;48(10):2006-12. doi: 10.1007/s00125-005-1892-2. Epub 2005 Aug 4.

Abstract

AIMS/HYPOTHESIS: Growing evidence suggests that the traits comprising the metabolic syndrome have a genetic basis. However, studies of genetic contributions to the syndrome are sparse. Against this background, we sought to estimate the heritability of the metabolic syndrome and its component traits.

MATERIALS AND METHODS

We investigated 803 subjects from 89 Caribbean-Hispanic families who have enrolled to date in the current Northern Manhattan Family Study and for whom metabolic syndrome information was available. Metabolic syndrome was defined in accordance with the National Cholesterol Education Program Adult Treatment Panel III (NCEP/ATPIII) criteria. Variance component methods were used to estimate age and sex-adjusted heritability of the metabolic syndrome and its components. To obtain the structures underlying the metabolic syndrome, we performed principal component factor analyses using six quantitative phenotypes included in the ATPIII definition.

RESULTS

The heritability for the metabolic syndrome was 24% (p=0.009), and ranged from 16 to 60% for its five components. Factor analysis yielded two independent factors (factor 1: lipids/glucose/obesity; factor 2: blood pressure). Heritability analysis revealed significant genetic effects on both factors (44% for lipids/glucose/obesity, and 20% for blood pressure).

CONCLUSIONS/INTERPRETATION: In the Caribbean-Hispanic families investigated, we demonstrated moderate and significant heritabilities for the metabolic syndrome itself, as well as for individual components and independent factors of the syndrome. These results provide evidence that could support future tasks of mapping susceptibility loci for this syndrome.

摘要

目的/假设:越来越多的证据表明,构成代谢综合征的特征具有遗传基础。然而,关于该综合征遗传贡献的研究却很少。在此背景下,我们试图估算代谢综合征及其组成特征的遗传度。

材料与方法

我们调查了来自89个加勒比裔西班牙家庭的803名受试者,这些家庭均已参与目前的北曼哈顿家庭研究,且有代谢综合征相关信息。代谢综合征依据美国国家胆固醇教育计划成人治疗组第三次报告(NCEP/ATPIII)标准进行定义。采用方差成分法估算代谢综合征及其组成部分经年龄和性别调整后的遗传度。为了获取代谢综合征背后的结构,我们使用ATPIII定义中包含的六种定量表型进行主成分因子分析。

结果

代谢综合征的遗传度为24%(p = 0.009),其五个组成部分的遗传度在16%至60%之间。因子分析产生了两个独立因子(因子1:脂质/葡萄糖/肥胖;因子2:血压)。遗传度分析显示两个因子均有显著的遗传效应(脂质/葡萄糖/肥胖为44%,血压为20%)。

结论/解读:在我们调查的加勒比裔西班牙家庭中,我们证明了代谢综合征本身以及该综合征的各个组成部分和独立因子具有中度且显著的遗传度。这些结果为支持该综合征易感基因座定位的未来研究任务提供了证据。

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