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在美国按种族/民族划分的代谢综合征及其定量特征的遗传关联。

Genetic associations with metabolic syndrome and its quantitative traits by race/ethnicity in the United States.

机构信息

General Medicine Division, Massachusetts General Hospital, Boston, USA.

出版信息

Metab Syndr Relat Disord. 2011 Dec;9(6):475-82. doi: 10.1089/met.2011.0021. Epub 2011 Aug 17.

Abstract

BACKGROUND

Elevated insulin resistance (IR), triglycerides (TG), body mass index (BMI), and waist circumference (WC) are features of the metabolic syndrome. Although several single-nucleotide polymorphisms (SNPs) associated with these traits have been reported, no study has reported their risk allele frequencies and effect sizes among the major U.S. race/ethnic groups in a nationally representative sample.

METHODS

We compared the risk allele frequencies of eight SNPs previously associated with IR, TG, BMI, or WC by race/ethnicity (non-Hispanic white, non-Hispanic black, Mexican American) in 3,030 participants of the National Health and Nutrition Examination Study III (NHANES III). In regression models predicting IR, TG, BMI, WC, and metabolic syndrome, we tested whether the SNP effect sizes on these traits varied by race/ethnicity.

RESULTS

Risk allele frequencies varied by race/ethnicity for all eight loci (P<0.0001). The directionality of effects of the variants on IR, TG, WC, and BMI was generally consistent with previous observations and did not differ by race/ethnicity (P>0.001), although our study had low power for this test. No SNP predicted metabolic syndrome in any of the three groups (P>0.05).

CONCLUSIONS

The significance of racial/ethnic differences in risk allele frequencies merits consideration if genetic discoveries are to have clinical and public health applicability.

摘要

背景

胰岛素抵抗(IR)、甘油三酯(TG)、体重指数(BMI)和腰围(WC)升高是代谢综合征的特征。尽管已经报道了几种与这些特征相关的单核苷酸多态性(SNP),但没有研究在具有全国代表性的样本中报告这些主要美国种族/族裔群体的风险等位基因频率和效应大小。

方法

我们比较了 National Health and Nutrition Examination Study III(NHANES III)中 3030 名参与者中 8 个先前与 IR、TG、BMI 或 WC 相关的 SNP 按种族/族裔(非西班牙裔白人、非西班牙裔黑人、墨西哥裔美国人)的风险等位基因频率。在预测 IR、TG、BMI、WC 和代谢综合征的回归模型中,我们测试了 SNP 对这些特征的效应大小是否因种族/族裔而异。

结果

所有 8 个位点的风险等位基因频率均因种族/族裔而异(P<0.0001)。变体对 IR、TG、WC 和 BMI 的影响方向与先前的观察结果基本一致,并且不因种族/族裔而异(P>0.001),尽管我们的研究对此测试的效力较低。没有 SNP 在这三个群体中的任何一个中预测代谢综合征(P>0.05)。

结论

如果遗传发现具有临床和公共卫生适用性,那么考虑风险等位基因频率的种族/族裔差异的重要性是值得的。

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