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常见的 GCK、GCKR、G6PC2-ABCB11 和 MTNR1B 基因座的变异与两个亚洲人群的空腹血糖相关。

Common variants at the GCK, GCKR, G6PC2-ABCB11 and MTNR1B loci are associated with fasting glucose in two Asian populations.

机构信息

Department of Gene Diagnostics and Therapeutics, Research Institute, International Medical Center of Japan, 1-21-1 Toyama, Shinjuku-ku, Tokyo 162-8655, Japan.

出版信息

Diabetologia. 2010 Feb;53(2):299-308. doi: 10.1007/s00125-009-1595-1. Epub 2009 Nov 25.

Abstract

AIMS/HYPOTHESIS: To test fasting glucose association at four loci recently identified or verified by genome-wide association (GWA) studies of European populations, we performed a replication study in two Asian populations.

METHODS

We genotyped five common variants previously reported in Europeans: rs1799884 (GCK), rs780094 (GCKR), rs560887 (G6PC2-ABCB11) and both rs1387153 and rs10830963 (MTNR1B) in the general Japanese (n = 4,813) and Sri Lankan (n = 2,319) populations. To identify novel variants, we further examined genetic associations near each locus by using GWA scan data on 776 non-diabetic Japanese samples.

RESULTS

Fasting glucose association was replicated for the five single nucleotide polymorphisms (SNPs) at p < 0.05 (one-tailed test) in South Asians (Sri Lankan) as well as in East Asians (Japanese). In fine-mapping by GWA scan data, we identified in the G6PC2-ABCB11 region a novel SNP, rs3755157, with significant association in Japanese (p = 2.6 x 10(-8)) and Sri Lankan (p = 0.001) populations. The strength of association was more prominent at rs3755157 than that of the original SNP rs560887, with allelic heterogeneity detected between the SNPs. On analysing the cumulative effect of associated SNPs, we found the per-allele gradients (beta = 0.055 and 0.069 mmol/l in Japanese and Sri Lankans, respectively) to be almost equivalent to those reported in Europeans.

CONCLUSIONS/INTERPRETATION: Fasting glucose association at four tested loci was proven to be replicable across ethnic groups. Despite this overall consistency, ethnic diversity in the pattern and strength of linkage disequilibrium certainly exists and can help to appreciably reduce potential causal variants after GWA studies.

摘要

目的/假设:为了测试在欧洲人群全基因组关联研究(GWA)中最近确定或验证的四个基因座的空腹血糖关联,我们在两个亚洲人群中进行了一项复制研究。

方法

我们对之前在欧洲人报告的五个常见变异进行了基因分型:rs1799884(GCK)、rs780094(GCKR)、rs560887(G6PC2-ABCB11)以及 rs1387153 和 rs10830963(MTNR1B)。为了鉴定新的变异,我们进一步使用 776 名非糖尿病日本样本的 GWA 扫描数据,对每个基因座附近的遗传关联进行了研究。

结果

在南亚人(斯里兰卡人)和东亚人(日本人)中,五个单核苷酸多态性(SNP)的空腹血糖关联在 p < 0.05(单侧检验)得到了复制。通过 GWA 扫描数据的精细作图,我们在 G6PC2-ABCB11 区域鉴定出了一个新的 SNP rs3755157,在日本人(p = 2.6 x 10(-8)) 和斯里兰卡人(p = 0.001)中均具有显著的关联。与原始 SNP rs560887 相比,rs3755157 的关联更强,并且在 SNP 之间检测到等位基因异质性。在分析相关 SNP 的累积效应时,我们发现每个等位基因的梯度(日本人中为 0.055mmol/l,斯里兰卡人为 0.069mmol/l)与欧洲人报告的结果几乎相当。

结论/解释:在四个测试基因座上的空腹血糖关联被证明在不同种族之间具有可复制性。尽管存在这种总体一致性,但连锁不平衡的模式和强度在种族之间确实存在多样性,并且可以在 GWA 研究后显著减少潜在的因果变异。

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