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LIPC基因rs493258多态性与年龄相关性黄斑变性易感性之间的关联

The Association between LIPC rs493258 Polymorphism and the Susceptibility to Age-Related Macular Degeneration.

作者信息

Wang Yafeng, Wang Mingxu, Zhang Xiaoqing, Nie Jing, Zhang Ming, Liu Xiaohong, Ma Le

机构信息

The First Affiliated Hospital of Xi'an Jiaotong University, College of Medicine, Xi'an Jiaotong University, Xi'an 710061, China.

Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, Xi'an 710004, China.

出版信息

Int J Environ Res Public Health. 2016 Oct 18;13(10):1022. doi: 10.3390/ijerph13101022.

Abstract

The purpose of this study was to evaluate the association of the hepatic lipase (LIPC) rs493258 polymorphism and susceptibility to age-related macular degeneration (AMD). A systematic search in PubMed, EMBASE, and ISI web of science databases was performed to identify eligible published studies without language restrictions up to April 2016. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) in different stages of AMD were estimated under different genetic models using meta-analytic methods. Seven studies comprising 20,559 cases and 17,200 controls met the inclusion criteria and were included in the meta-analysis. The LIPC rs493258 polymorphism showed a significant association with a lower risk of AMD under the allelic model (OR = 0.87, 95% CI = 0.84-0.90). Significant relationships between the variant and AMD were also observed in other genetic models (OR ranging from 0.71 to 0.86, all < 0.05). Stratified analysis based on ethnicity found that LIPC rs493258 polymorphism had a significant association with the decreased risk of the disease in the Caucasian population, but not in the Asian population. For late AMD, significant associations of the rs493258 polymorphism with a lower risk of this disease were also observed in the allelic genetic model (OR = 0.87, 95% CI = 0.83-0.90). This meta-analysis demonstrates that the T allele in the LIPC rs493258 polymorphism was significantly associated with the risk of any and late AMD. The associations of the locus with early and late AMD risk in various populations need further exploration.

摘要

本研究旨在评估肝脂酶(LIPC)rs493258基因多态性与年龄相关性黄斑变性(AMD)易感性之间的关联。我们在PubMed、EMBASE和ISI科学网数据库中进行了系统检索,以识别截至2016年4月符合条件的已发表研究,检索无语言限制。使用荟萃分析方法,在不同遗传模型下估计AMD不同阶段的合并比值比(OR)及其95%置信区间(CI)。七项研究共纳入20559例病例和17200例对照,符合纳入标准并被纳入荟萃分析。在等位基因模型下,LIPC rs493258基因多态性与较低的AMD风险显著相关(OR = 0.87,95% CI = 0.84 - 0.90)。在其他遗传模型中也观察到该变异与AMD之间存在显著关系(OR范围为0.71至0.86,均<0.05)。基于种族的分层分析发现,LIPC rs493258基因多态性与白种人群中疾病风险降低显著相关,但在亚洲人群中无此关联。对于晚期AMD,在等位基因遗传模型中也观察到rs493258基因多态性与较低的疾病风险显著相关(OR = 0.87,95% CI = 0.83 - 0.90)。这项荟萃分析表明,LIPC rs493258基因多态性中的T等位基因与任何阶段及晚期AMD的风险显著相关。该基因座与不同人群中早期和晚期AMD风险的关联需要进一步探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa31/5086761/948d9ae01d7f/ijerph-13-01022-g001.jpg

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