Liu Ke, He Wenling, Zhao Jun, Zeng Yingxia, Cheng Hongbo
Shenzhen Key Laboratory of Ophthalmology, Shenzhen Eye Hospital Affiliated to Jinan University School of Ophthalmology & Optometry Affiliated to Shenzhen University, Shenzhen, Guangdong, China.
Medicine (Baltimore). 2017 Jun;96(26):e7291. doi: 10.1097/MD.0000000000007291.
The association of the WDR36 gene with glaucoma has been controversial in the literature. We therefore conducted a systematic review and meta-analysis to assess the association of all reported common polymorphisms in WDR36 with primary open angle glaucoma (POAG) and its subtypes: high tension glaucoma (HTG) and normal tension glaucoma (NTG).
Publications in PUBMED and EMBASE databases up to March 9, 2016 were searched for case-control association studies of WDR36 with POAG, HTG, and/or NTG. Reported studies giving adequate genotype and/or allele information were included. Pooled odds ratios (ORs) and 95% confidence intervals (CIs) of individual polymorphisms were estimated using the allelic model.
Our literature search yielded 122 records, among which 5 studies were eligible for meta-analysis, involving a total of 1352 POAG patients and 894 controls. Five WDR36 polymorphisms were meta-analyzed, rs11241095, rs10038177, rs17553936, rs13186912, and rs13153937. However, none of them was significantly associated with POAG, HTG, or NTG. The most-investigated polymorphisms, rs11241095 and rs10038177, had a pooled-OR of 1.09 (95% CI: 0.94-1.28, P = .25, I = 0) and 0.99 (95% CI: 0.71-1.39, P = .97, I = 77%), respectively, for POAG.
The existing data in the literature do not support a significant role of WDR36 in the genetic susceptibility of POAG or its subtypes. Further replication studies in specific populations are warranted.
WDR36基因与青光眼的关联在文献中一直存在争议。因此,我们进行了一项系统综述和荟萃分析,以评估WDR36中所有已报道的常见多态性与原发性开角型青光眼(POAG)及其亚型:高眼压性青光眼(HTG)和正常眼压性青光眼(NTG)之间的关联。
检索截至2016年3月9日在PUBMED和EMBASE数据库中的文献,以查找WDR36与POAG、HTG和/或NTG的病例对照关联研究。纳入报道了足够基因型和/或等位基因信息的研究。使用等位基因模型估计个体多态性的合并比值比(OR)和95%置信区间(CI)。
我们的文献检索产生了122条记录,其中5项研究符合荟萃分析的条件,共涉及1352例POAG患者和894例对照。对5个WDR36多态性进行了荟萃分析,分别为rs11241095、rs10038177、rs17553936、rs13186912和rs13153937。然而,它们均与POAG、HTG或NTG无显著关联。研究最多的多态性rs11241095和rs10038177,对于POAG的合并OR分别为1.09(95%CI:0.94 - 1.28,P = 0.25,I = 0)和0.99(95%CI:0.71 - 1.39,P = 0.97,I = 77%)。
文献中的现有数据不支持WDR36在POAG或其亚型的遗传易感性中起重要作用。有必要在特定人群中进行进一步的重复研究。