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撒哈拉以南非洲人群中全基因组关联研究相关的2型糖尿病易感位点评估。

Evaluation of Genome Wide Association Study Associated Type 2 Diabetes Susceptibility Loci in Sub Saharan Africans.

作者信息

Adeyemo Adebowale A, Tekola-Ayele Fasil, Doumatey Ayo P, Bentley Amy R, Chen Guanjie, Huang Hanxia, Zhou Jie, Shriner Daniel, Fasanmade Olufemi, Okafor Godfrey, Eghan Benjamin, Agyenim-Boateng Kofi, Adeleye Jokotade, Balogun Williams, Elkahloun Abdel, Chandrasekharappa Settara, Owusu Samuel, Amoah Albert, Acheampong Joseph, Johnson Thomas, Oli Johnnie, Adebamowo Clement, Collins Francis, Dunston Georgia, Rotimi Charles N

机构信息

Center for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health Bethesda, MD, USA.

Department of Medicine, University of Lagos Lagos, Nigeria.

出版信息

Front Genet. 2015 Nov 24;6:335. doi: 10.3389/fgene.2015.00335. eCollection 2015.

Abstract

Genome wide association studies (GWAS) for type 2 diabetes (T2D) undertaken in European and Asian ancestry populations have yielded dozens of robustly associated loci. However, the genomics of T2D remains largely understudied in sub-Saharan Africa (SSA), where rates of T2D are increasing dramatically and where the environmental background is quite different than in these previous studies. Here, we evaluate 106 reported T2D GWAS loci in continental Africans. We tested each of these SNPs, and SNPs in linkage disequilibrium (LD) with these index SNPs, for an association with T2D in order to assess transferability and to fine map the loci leveraging the generally reduced LD of African genomes. The study included 1775 unrelated Africans (1035 T2D cases, 740 controls; mean age 54 years; 59% female) enrolled in Nigeria, Ghana, and Kenya as part of the Africa America Diabetes Mellitus (AADM) study. All samples were genotyped on the Affymetrix Axiom PanAFR SNP array. Forty-one of the tested loci showed transferability to this African sample (p < 0.05, same direction of effect), 11 at the exact reported SNP and 30 others at SNPs in LD with the reported SNP (after adjustment for the number of tested SNPs). TCF7L2 SNP rs7903146 was the most significant locus in this study (p = 1.61 × 10(-8)). Most of the loci that showed transferability were successfully fine-mapped, i.e., localized to smaller haplotypes than in the original reports. The findings indicate that the genetic architecture of T2D in SSA is characterized by several risk loci shared with non-African ancestral populations and that data from African populations may facilitate fine mapping of risk loci. The study provides an important resource for meta-analysis of African ancestry populations and transferability of novel loci.

摘要

在欧洲和亚洲血统人群中开展的2型糖尿病(T2D)全基因组关联研究(GWAS)已经发现了数十个与之密切相关的基因座。然而,在撒哈拉以南非洲(SSA)地区,T2D的基因组学研究仍很匮乏,该地区T2D发病率正在急剧上升,且环境背景与之前这些研究中的地区截然不同。在此,我们对非洲大陆人群中报道的106个T2D GWAS基因座进行评估。我们检测了这些单核苷酸多态性(SNP)中的每一个,以及与这些索引SNP处于连锁不平衡(LD)状态的SNP,以确定其与T2D的关联,从而评估其可转移性,并利用非洲基因组中普遍较低的LD对基因座进行精细定位。该研究纳入了1775名无亲缘关系的非洲人(1035例T2D患者,740名对照;平均年龄54岁;59%为女性),他们来自尼日利亚、加纳和肯尼亚,是非洲裔美国人糖尿病(AADM)研究的一部分。所有样本均在Affymetrix Axiom PanAFR SNP芯片上进行基因分型。41个检测的基因座在这个非洲样本中显示出可转移性(p < 0.05,效应方向相同),其中11个在确切报道的SNP处,另外30个在与报道的SNP处于LD状态的SNP处(在对检测的SNP数量进行校正后)。TCF7L2基因的SNP rs7903146是本研究中最显著的基因座(p = 1.61 × 10(-8))。大多数显示出可转移性的基因座都成功地进行了精细定位,即定位到比原始报道中更小的单倍型。研究结果表明,SSA地区T2D的遗传结构特征是存在几个与非非洲祖先人群共有的风险基因座,并且来自非洲人群的数据可能有助于对风险基因座进行精细定位。该研究为非洲血统人群的荟萃分析和新基因座的可转移性提供了重要资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a003/4656823/86d2769754b1/fgene-06-00335-g0001.jpg

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