Nannini Drew R, Torres Mina, Chen Yii-Der I, Taylor Kent D, Rotter Jerome I, Varma Rohit, Gao Xiaoyi
Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, Illinois, United States.
USC Roski Eye Institute, Department of Ophthalmology, University of Southern California, Los Angeles, California, United States.
Invest Ophthalmol Vis Sci. 2017 Jan 1;58(1):87-95. doi: 10.1167/iovs.16-19891.
Vertical cup-disc ratio (VCDR) is used as a clinical assessment measure to identify and monitor glaucomatous damage to the optic nerve. Previous genetic studies conducted in European and Asian populations have identified many loci associated with VCDR. The genetic factors in other ethnic populations, such as Latino, influencing VCDR remain to be determined. Here, we describe the first genome-wide association study (GWAS) on VCDR in Latino individuals.
We conducted this GWAS on VCDR using 4537 Latino individuals who were genotyped by using either the Illumina OmniExpress BeadChip (∼730K markers) or the Illumina Hispanic/SOL BeadChip (∼2.5 million markers). Study subjects were 40 years of age and older. Linear regression, adjusting for age, sex, and principal components of genetic ancestry, was conducted to assess the associations between single nucleotide polymorphisms (SNPs) and VCDR. We imputed SNPs from the 1000 Genomes Project to integrate additional SNPs not directly genotyped.
We replicated two previously reported SNPs that reached GWAS significance, rs1900005 and rs7916697, in the ATOH7-PBLD region, as well as identified two suggestive associations in the CDC7-TGFBR3 region on chromosome 1p22.1 and in the ZNF770-DPH6 region on chromosome 15q14. We discovered a novel SNP, rs56238729 (P = 1.22 × 10-13), in the ATOH7-PBLD region that is significantly associated with VCDR in Latino individuals. We replicated eight previously reported regions, including COL8A1, CDKN2B-CDKN2BAS, BMP2, and CHEK2 (P < 2.17 × 10-3).
Our results discovered a novel SNP that is significantly associated with VCDR in Latino individuals and confirmed previously reported loci, providing further insight into the genetic architecture of VCDR.
垂直杯盘比(VCDR)用作临床评估指标,以识别和监测青光眼对视神经的损害。此前在欧洲和亚洲人群中开展的基因研究已确定了许多与VCDR相关的基因座。其他种族人群(如拉丁裔)中影响VCDR的遗传因素仍有待确定。在此,我们描述了针对拉丁裔个体VCDR的首个全基因组关联研究(GWAS)。
我们使用4537名拉丁裔个体开展了这项关于VCDR的GWAS,这些个体通过Illumina OmniExpress BeadChip(约73万个标记)或Illumina Hispanic/SOL BeadChip(约250万个标记)进行基因分型。研究对象年龄在40岁及以上。进行线性回归分析,并对年龄、性别和遗传血统的主成分进行校正,以评估单核苷酸多态性(SNP)与VCDR之间的关联。我们从千人基因组计划中推算SNP,以整合未直接进行基因分型的其他SNP。
我们在ATOH7 - PBLD区域重复了两个先前报道的达到GWAS显著性水平的SNP,即rs1900005和rs7916697,同时在1号染色体p22.1的CDC7 - TGFBR3区域和15号染色体q14的ZNF770 - DPH6区域发现了两个提示性关联。我们在ATOH7 - PBLD区域发现了一个新的SNP,rs56238729(P = 1.22×10 - 13),它在拉丁裔个体中与VCDR显著相关。我们重复了八个先前报道的区域,包括COL8A1、CDKN2B - CDKN2BAS、BMP2和CHEK2(P < 2.17×10 - 3)。
我们的结果发现了一个在拉丁裔个体中与VCDR显著相关的新SNP,并证实了先前报道的基因座,为VCDR的遗传结构提供了进一步的见解。