Suppr超能文献

非洲人增殖性糖尿病视网膜病变的全基因组关联研究。

Genome-wide association study for proliferative diabetic retinopathy in Africans.

作者信息

Liu Chang, Chen Guanjie, Bentley Amy R, Doumatey Ayo, Zhou Jie, Adeyemo Adebowale, Yang Jinkui, Rotimi Charles

机构信息

1The Center for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD USA.

2Department of Endocrinology, Beijing Tongren Hospital, Capital Medical University, Beijing, 10730 China.

出版信息

NPJ Genom Med. 2019 Aug 29;4:20. doi: 10.1038/s41525-019-0094-7. eCollection 2019.

Abstract

Proliferative diabetic retinopathy (PDR) is a sight-threatening complication of diabetes that is associated with longer duration of diabetes and poor glycemic control under a genetic susceptibility background. Although GWAS of PDR have been conducted in Europeans and Asians, none has been done in continental Africans, a population at increased risk for PDR. Here, we report a GWAS of PDR among Africans. PDR cases ( = 64) were T2D patients with neovascularization in the retina and/or retinal detachment. Controls ( = 227) were T2D patients without listed eye complications despite high risk (T2D duration ≥10 years and fasting blood glucose >169 mg/dl). Replication was assessed in African Americans enrolled in the ARIC study. We identified 4 significant loci: WDR72, HLA-B, GAP43/RP11-326J18.1, and AL713866.1. At WDR72 the most strongly associated SNPs were rs12906891 (MAF = 0.071;  = 9.68 × 10-10; OR = 1.46, 95% CI [1.30,1.64]) and rs11070992 (MAF = 0.14;  = 4.23 × 10; OR = 1.28, 95%CI [1.17-1.40]). rs11070992 replicated in African Americans ( = 0.04). Variants in this gene have been associated with diabetic retinopathy, glycemic control, revascularization, and kidney disease.

摘要

增殖性糖尿病视网膜病变(PDR)是糖尿病的一种威胁视力的并发症,在遗传易感性背景下,它与糖尿病病程较长及血糖控制不佳有关。尽管已在欧洲人和亚洲人中开展了PDR的全基因组关联研究(GWAS),但尚未在非洲大陆人群中进行,而该人群患PDR的风险增加。在此,我们报告了一项在非洲人群中开展的PDR的GWAS研究。PDR病例(n = 64)为视网膜出现新生血管和/或视网膜脱离的2型糖尿病患者。对照组(n = 227)为尽管存在高风险(2型糖尿病病程≥10年且空腹血糖>169 mg/dl)但未列出眼部并发症的2型糖尿病患者。在参加动脉粥样硬化风险社区(ARIC)研究的非裔美国人中评估了重复性。我们鉴定出4个显著位点:WDR72、HLA - B、GAP43/RP11 - 326J18.1和AL713866.1。在WDR72基因座,关联最强的单核苷酸多态性(SNP)是rs12906891(小等位基因频率[MAF] = 0.071;P = 9.68×10 - 10;比值比[OR] = 1.46,95%置信区间[CI][1.30,1.64])和rs11070992(MAF = 0.14;P = 4.23×10;OR = 1.28,95%CI[1.17 - 1.40])。rs11070992在非裔美国人中得到重复性验证(P = 0.04)。该基因中的变异与糖尿病视网膜病变、血糖控制、血管再生和肾脏疾病有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bb2/6715701/c6bf0d32ffb0/41525_2019_94_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验