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丝氨酸消旋酶基因变异与中国汉族 2 型糖尿病的相关性研究。

Association of serine racemase gene variants with type 2 diabetes in the Chinese Han population.

机构信息

Department of Endocrinology and Metabolism Peking University People's Hospital Peking University Diabetes Center Beijing China.

China-Japan Friendship Hospital Beijing China.

出版信息

J Diabetes Investig. 2014 May 4;5(3):286-9. doi: 10.1111/jdi.12145. Epub 2013 Nov 15.

DOI:10.1111/jdi.12145
PMID:24843776
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4020332/
Abstract

A genome-wide association study in the Chinese Han population has identified several novel genetic variants of the serine racemase (SRR) gene in type 2 diabetes. Our purpose was to systematically evaluate the contribution of SRR variants in the Chinese Han population. rs391300 and rs4523957 in SRR were genotyped respectively in the two independent populations. A meta-analysis was used to estimate the effects of SRR in 21,305 Chinese Han individuals. Associations between single-nucleotide polymorphisms and diabetes-related phenotypes were analyzed among 2,615 newly diagnosed type 2 diabetes patients and 5,029 controls. Neither rs391300 nor rs4523957 were associated with type 2 diabetes in populations. Furthermore, meta-analysis did not confirm an association between type 2 diabetes and SRR. In the controls, rs391300-A and rs4523957-G were associated with higher 30-min plasma glucose in an oral glucose tolerance test. The present study did not confirm that SRR was associated with type 2 diabetes.

摘要

一项全基因组关联研究在中国汉族人群中鉴定出了几种新型丝氨酸消旋酶(SRR)基因的遗传变异与 2 型糖尿病有关。我们的目的是系统地评估 SRR 变异在中国汉族人群中的作用。分别在两个独立的人群中对 SRR 的 rs391300 和 rs4523957 进行了基因分型。采用荟萃分析来估计 21305 名中国汉族个体中 SRR 的作用。在 2615 名新诊断的 2 型糖尿病患者和 5029 名对照中分析了单核苷酸多态性与糖尿病相关表型之间的关系。rs391300 或 rs4523957 在人群中均与 2 型糖尿病无关。此外,荟萃分析也未证实 SRR 与 2 型糖尿病之间存在关联。在对照组中,口服葡萄糖耐量试验中 rs391300-A 和 rs4523957-G 与较高的 30 分钟血浆葡萄糖水平相关。本研究并未证实 SRR 与 2 型糖尿病有关。

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本文引用的文献

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Diabetes. 2013 Jan;62(1):291-8. doi: 10.2337/db12-0454. Epub 2012 Sep 6.
2
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.大规模的关联分析确定了影响血糖特征的新基因座,并深入了解了潜在的生物学途径。
Nat Genet. 2012 Sep;44(9):991-1005. doi: 10.1038/ng.2385. Epub 2012 Aug 12.
3
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians.全基因组关联研究的荟萃分析确定了东亚人群 2 型糖尿病的 8 个新位点。
Nat Genet. 2011 Dec 11;44(1):67-72. doi: 10.1038/ng.1019.
4
A genome-wide association study confirms previously reported loci for type 2 diabetes in Han Chinese.一项全基因组关联研究证实了汉族 2 型糖尿病的先前报道的易感位点。
PLoS One. 2011;6(7):e22353. doi: 10.1371/journal.pone.0022353. Epub 2011 Jul 22.
5
Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.多族群东南亚队列中 2 型糖尿病关联位点的可转移性。
PLoS Genet. 2011 Apr;7(4):e1001363. doi: 10.1371/journal.pgen.1001363. Epub 2011 Apr 7.
6
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7
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Diabet Med. 2009 Dec;26(12):1262-8. doi: 10.1111/j.1464-5491.2009.02831.x.