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人类尿素转运蛋白-2 的遗传变异与亚洲人群的代谢综合征有关。

Genetic variants of human urea transporter-2 are associated with metabolic syndrome in Asian population.

机构信息

Division of Biostatistics and Bioinformatics, Institute of Population Health Sciences, Zhunan, Taiwan.

出版信息

Clin Chim Acta. 2010 Dec 14;411(23-24):2009-13. doi: 10.1016/j.cca.2010.08.025. Epub 2010 Aug 23.

Abstract

BACKGROUND

A previous study has reported that the Ile227 and Ala357 genetic variants of human urea transporter-2 (HUT2) were associated with blood pressure in males in Asian population. In this study, we aimed to investigate five known HUT2 genetic variants with metabolic syndrome (MetS) and its related traits in the Stanford Asia-Pacific Program for Hypertension and Insulin Resistance (SAPPHIRe) study cohort.

METHODS

Five HUT2 single nucleotide polymorphisms (SNPs) were selected and genotyped among 1791 subjects in the SAPPHIRe study cohort. We first computed allele frequency and performed Hardy-Weinberg equilibrium (HWE) test in controls for each SNP. Next, we tested genotype associations with metabolic syndrome using multiple generalized estimating equations (GEE) models with covariate adjustment. Furthermore, multi-marker and multi-trait association tests were carried out using FBAT program. To account for multiple testing, Bonferroni correction was applied in this study.

RESULTS

Among those 5 HUT2 SNPs, SNPs 1, 2 and 3 were significantly associated with MetS in the total sample and females, separately (9×10(-4)≤p≤0.04), but only the association between SNP 1 and MetS in females remained statistically significant after Bonferroni correction. When testing 5 SNPs simultaneously, significant associations were found with triglycerides (TG) (p=0.04). Likewise, significant multi-trait association (combining the data of waist circumference, TG, high density lipoprotein (HDL) cholesterol and fasting glucose together) was found with SNP 2 (p=0.04), but both results of multi-maker and multi-trait associations did not remain significant after multiple testing correction.

CONCLUSION

The results have provided evidence that the HUT2 gene may play a certain role in developing MetS and its related traits in Asian population. Further investigation of the HUT2 gene influencing MetS and its related traits will be warranted.

摘要

背景

先前的研究表明,人类尿素转运蛋白 2(HUT2)的 Ile227 和 Ala357 遗传变异与亚洲男性的血压有关。在这项研究中,我们旨在研究斯坦福亚太高血压和胰岛素抵抗计划(SAPPHIRe)研究队列中已知的五个 HUT2 遗传变异与代谢综合征(MetS)及其相关特征的关系。

方法

在 SAPPHIRe 研究队列的 1791 名受试者中选择并检测了五个 HUT2 单核苷酸多态性(SNP)。我们首先计算了每个 SNP 在对照组中的等位基因频率并进行了 Hardy-Weinberg 平衡(HWE)检验。接下来,我们使用多变量广义估计方程(GEE)模型进行了基因型与代谢综合征的关联检验,并进行了协变量调整。此外,使用 FBAT 程序进行了多标记和多特征关联检验。为了进行多重检验,本研究应用了 Bonferroni 校正。

结果

在这 5 个 HUT2 SNP 中,SNP1、2 和 3 分别在总样本和女性中与 MetS 显著相关(9×10(-4)≤p≤0.04),但只有 SNP1 与女性 MetS 的关联在 Bonferroni 校正后仍具有统计学意义。当同时检测 5 个 SNP 时,发现与甘油三酯(TG)显著相关(p=0.04)。同样,与 SNP2 显著相关(p=0.04),但多标记和多特征关联分析的结果在多次检验校正后均不具有统计学意义。

结论

研究结果为 HUT2 基因在亚洲人群中可能对代谢综合征及其相关特征的发展具有一定作用提供了证据。需要进一步研究 HUT2 基因对代谢综合征及其相关特征的影响。

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