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CDKN2B基因rs1063192多态性降低青光眼风险。

CDKN2B gene rs1063192 polymorphism decreases the risk of glaucoma.

作者信息

Hu Zhenxian, He Chenliang

机构信息

Department of Ophthalmology, Tongde Hospital of Zhejiang Province, Hangzhou 310012, Zhejiang, China.

出版信息

Oncotarget. 2017 Mar 28;8(13):21167-21176. doi: 10.18632/oncotarget.15504.

DOI:10.18632/oncotarget.15504
PMID:28416752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5400574/
Abstract

The aim of this meta-analysis was to evaluate the association between cyclin-dependent kinase Inhibitor-2B (CDKN2B) gene rs1063192 polymorphism and glaucoma risk. We searched the databases of PubMed, and Embase. Pooled odds ratios (ORs) and 95% confidence intervals (CIs) were calculated by using fixed-effect or random-effect models. A total of 14 case-control studies involving 11,316 cases and 24,055 controls were included. Meta-analysis showed that CDKN2B gene rs1063192 polymorphism was associated with a decreased risk of glaucoma. Stratification analysis of ethnicity indicated that rs1063192 polymorphism decreased the risk of glaucoma among Caucasians and Asians. Stratification analysis by type of glaucoma revealed that rs1063192 polymorphism conferred a protective factor of primary open-angle glaucoma (POAG) and non-POAG. Stratification by source of controls uncovered an association between rs1063192 polymorphism and glaucoma in groups of population-based controls. In conclusion, this meta-analysis indicates that CDKN2B gene rs1063192 polymorphism is significantly associated with a decreased risk of glaucoma.

摘要

这项荟萃分析的目的是评估细胞周期蛋白依赖性激酶抑制剂2B(CDKN2B)基因rs1063192多态性与青光眼风险之间的关联。我们检索了PubMed和Embase数据库。使用固定效应或随机效应模型计算合并比值比(OR)和95%置信区间(CI)。共纳入14项病例对照研究,涉及11316例病例和24055例对照。荟萃分析表明,CDKN2B基因rs1063192多态性与青光眼风险降低相关。种族分层分析表明,rs1063192多态性降低了白种人和亚洲人患青光眼的风险。按青光眼类型进行的分层分析显示,rs1063192多态性是原发性开角型青光眼(POAG)和非POAG的保护因素。按对照来源进行分层发现,rs1063192多态性与基于人群对照的组中青光眼之间存在关联。总之,这项荟萃分析表明,CDKN2B基因rs1063192多态性与青光眼风险降低显著相关。

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本文引用的文献

1
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Genet Test Mol Biomarkers. 2016 Oct;20(10):637-641. doi: 10.1089/gtmb.2016.0140. Epub 2016 Aug 19.
2
Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma.9p21青光眼位点的基因关联导致正常眼压性青光眼中的性别差异。
Invest Ophthalmol Vis Sci. 2016 Jun 1;57(7):3416-21. doi: 10.1167/iovs.16-19401.
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A common variant near TGFBR3 is associated with primary open angle glaucoma.
J Inflamm Res. 2021 Jun 30;14:2865-2872. doi: 10.2147/JIR.S304801. eCollection 2021.
4
Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes.外显子组关联研究鉴定 FN3KRP 和 PGP 为新的候选长寿基因。
J Gerontol A Biol Sci Med Sci. 2021 Apr 30;76(5):786-795. doi: 10.1093/gerona/glab023.
5
Genetic association between CDKN2B/CDKN2B-AS1 gene polymorphisms with primary glaucoma in a North Indian cohort: an original study and an updated meta-analysis.CDKN2B/CDKN2B-AS1 基因多态性与北印度队列原发性青光眼的遗传关联:一项原始研究和更新的荟萃分析。
BMC Med Genomics. 2021 Jan 4;14(1):1. doi: 10.1186/s12920-020-00855-1.
6
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PLoS One. 2020 Jun 3;15(6):e0233692. doi: 10.1371/journal.pone.0233692. eCollection 2020.
转化生长因子β受体3(TGFBR3)附近的一个常见变异与原发性开角型青光眼相关。
Hum Mol Genet. 2015 Jul 1;24(13):3880-92. doi: 10.1093/hmg/ddv128. Epub 2015 Apr 10.
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Mol Vis. 2014 Nov 4;20:1471-9. eCollection 2014.
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Involvement of genetic variants associated with primary open-angle glaucoma in pathogenic mechanisms and family history of glaucoma.与原发性开角型青光眼相关的基因变异在青光眼致病机制及家族史中的作用。
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