Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong, China.
Department of Neurosurgery, Southwest Medical University, Luzhou, Sichuan, China.
Invest Ophthalmol Vis Sci. 2019 Jul 1;60(8):2914-2924. doi: 10.1167/iovs.18-26489.
To evaluate the association of single-nucleotide polymorphisms (SNPs) in the SIX1-SIX6 locus with primary open-angle glaucoma (POAG) through a systematic review and meta-analysis from 22 studies.
To our knowledge, all case-control association studies on SNPs in the SIX1-SIX6 locus and POAG reported up to August 30, 2018, in PubMed, Embase, and Web of Science were retrieved. Unadjusted and adjusted odds ratios (ORs) and 95% confidence intervals (95% CIs) for each SNP were calculated using a fixed- or random-effect model according to interstudy heterogeneity.
This meta-analysis involved 12 SNPs in SIX1-SIX6 reported in 22 studies. The association of rs10483727 with POAG has been presented in 16 studies involving 14,402 patients and 27,425 controls, whereas rs33912345 has been investigated in 12 studies involving 10,563 patients and 16,740 controls. Meta-analyses revealed significant associations of these two SNPs with POAG in the pooled populations under all genetic models. Stratified analyses by population detected significant association of both SNPs in the East Asian and Caucasian subgroups, but not in South Asian or African subgroups. Among the other SNPs that were reported by up to four cohorts of East Asian and African ancestries, only rs12436579 showed a significant association in the meta-analysis (OR = 0.79, P = 1.08 × 10-4).
This meta-analysis confirmed the association of rs10483727 and rs33912345 in SIX1-SIX6 with POAG. The associations of both SNPs were specifically detected in East Asian and Caucasian cohorts, rather than in South Asian and African cohorts, suggesting an ethnic difference. SNP rs12436579 is a candidate variant for the disease that awaits validation in other populations.
通过对截至 2018 年 8 月 30 日在 PubMed、Embase 和 Web of Science 上检索到的关于 SIX1-SIX6 基因座中单核苷酸多态性(SNP)与原发性开角型青光眼(POAG)的病例对照关联研究进行系统评价和荟萃分析,评估该基因座中 SNP 与 POAG 的相关性。
据我们所知,检索了截至 2018 年 8 月 30 日在 PubMed、Embase 和 Web of Science 上发表的所有关于 SIX1-SIX6 基因座中 SNP 与 POAG 的病例对照关联研究。根据研究间异质性,使用固定效应模型或随机效应模型计算每个 SNP 的未经调整和调整后的比值比(OR)和 95%置信区间(95%CI)。
该荟萃分析共纳入了 22 项研究中报道的 SIX1-SIX6 中的 12 个 SNP。rs10483727 与 POAG 的关联已在涉及 14402 例患者和 27425 例对照的 16 项研究中报道,而 rs33912345 已在涉及 10563 例患者和 16740 例对照的 12 项研究中进行了研究。荟萃分析显示,在汇总人群中,这两个 SNP 在所有遗传模型下均与 POAG 显著相关。按人群进行分层分析显示,这两个 SNP 均与东亚和高加索亚组相关,但与南亚或非洲亚组无关。在来自东亚和非洲血统的最多四个队列报道的其他 SNP 中,只有 rs12436579 在荟萃分析中显示出显著相关性(OR=0.79,P=1.08×10-4)。
本荟萃分析证实了 SIX1-SIX6 中的 rs10483727 和 rs33912345 与 POAG 之间的关联。这两个 SNP 的关联仅在东亚和高加索人群中被发现,而不是在南亚和非洲人群中,提示存在种族差异。SNP rs12436579 是该疾病的候选变异,尚需在其他人群中验证。