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ERCC2基因rs13181多态性与胶质瘤风险的关联:一项更新的荟萃分析

ERCC2 rs13181 Polymorphism Association with Glioma Risk: an Update Meta-Analysis.

作者信息

Salari Nader, Rasoulpoor Shna, Shabani Shervin, Mansouri Kamran, Bokaee Shadi, Fatahian Reza, Farshchian Negin, Mohammadi Masoud, Hosseinian-Far Melika

机构信息

Department of Biostatistics, School of Health, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Student Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran.

出版信息

Indian J Surg Oncol. 2023 Mar;14(1):60-68. doi: 10.1007/s13193-022-01623-6. Epub 2022 Aug 18.

DOI:10.1007/s13193-022-01623-6
PMID:36891435
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9986186/
Abstract

Glioma is the most common type of primary brain tumour which accounts for about 30% of all brain and central nervous system tumours, and approximately 70% of adult malignant brain tumours. Numerous studies have been performed to assess the relationship between ERCC2 rs13181 polymorphism and the risk of glioma development, yet these findings of these studies are often inconsistent and contradictory. Therefore, the aim of this study is to conduct a systematic review and meta-analysis to assess the role of ERCC2 rs13181 in glioma developing. In this work, we have conducted a systematic review and meta-analysis. In order to collect the results of relevant studies on the association of ERCC2 rs13181 gene polymorphism with glioma, we initially searched the Scopus, Embase, Web of Science (WoS), PubMed, and ScienceDirect databases, without a lower time limit, and until June 2020. In order to analyse the eligible studies, the random effects model was used and the heterogeneity of the studies was investigated with the index. Data analysis was performed within the Comprehensive Meta-Analysis software (version 2). The total number of studies that focused on patients with glioma was 10. The odds ratio of GG vs TT genotype in patients with glioma based on meta-analysis was 1.08 (0.85-1.37: 95% confidence interval), which indicates the increasing effect of GG vs TT genotype by 0.08. The odds ratio of GG + TG vs TT genotype in patients with glioma was 1.22 (1.38-1.7: 95% confidence interval) based on meta-analysis, which indicates the increasing effect of GG + TG vs TT genotype as 0.22. The odds ratio of TG vs TT genotype in patients with glioma was 1.2 (0.38-1.4: 95% confidence interval), which shows the increasing effect of TG vs TT genotype by 0.2. The odds ratio of G vs T genotype in patients with glioma based on the meta-analysis was 1.15 (1.26-1.4: 95% confidence interval), which indicates the increasing effect of G vs T genotype by 0.15. The odds ratio of GG vs TG + TT genotype in patients with glioma based on meta-analysis was 1.22 (1.33-1.45: 95% confidence interval), which indicates the increasing effect of GG vs TG + TT genotype by 0.22. The results of this systematic review and meta-analysis show that ERCC2 rs13181 polymorphism and its genotypes are an important risk factor for genetic susceptibility to glioma tumour.

摘要

胶质瘤是最常见的原发性脑肿瘤类型,约占所有脑和中枢神经系统肿瘤的30%,约占成人恶性脑肿瘤的70%。已经进行了大量研究来评估ERCC2 rs13181多态性与胶质瘤发生风险之间的关系,但这些研究结果往往不一致且相互矛盾。因此,本研究的目的是进行系统评价和荟萃分析,以评估ERCC2 rs13181在胶质瘤发生中的作用。在这项工作中,我们进行了系统评价和荟萃分析。为了收集关于ERCC2 rs13181基因多态性与胶质瘤关联的相关研究结果,我们最初检索了Scopus、Embase、科学引文索引(WoS)、PubMed和ScienceDirect数据库,没有时间下限,直至2020年6月。为了分析符合条件的研究,使用了随机效应模型,并使用I2指数研究了研究的异质性。数据分析在综合荟萃分析软件(版本2)中进行。专注于胶质瘤患者的研究总数为10项。基于荟萃分析,胶质瘤患者中GG与TT基因型的优势比为1.08(0.85 - 1.37:95%置信区间),这表明GG与TT基因型的效应增加了0.08。基于荟萃分析,胶质瘤患者中GG + TG与TT基因型的优势比为1.22(1.38 - 1.7:95%置信区间),这表明GG + TG与TT基因型的效应增加了0.22。胶质瘤患者中TG与TT基因型的优势比为1.2(0.38 - 1.4:95%置信区间),这表明TG与TT基因型的效应增加了0.2。基于荟萃分析,胶质瘤患者中G与T基因型的优势比为1.15(1.26 - 1.4:95%置信区间),这表明G与T基因型的效应增加了0.15。基于荟萃分析,胶质瘤患者中GG与TG + TT基因型的优势比为1.22(1.33 - 1.45:95%置信区间),这表明GG与TG + TT基因型的效应增加了0.22。这项系统评价和荟萃分析的结果表明,ERCC2 rs13181多态性及其基因型是胶质瘤肿瘤遗传易感性的重要危险因素。

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