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肿瘤坏死因子-α-308G/A多态性与食管癌风险之间的关联:一项更新的荟萃分析和试验序贯分析

Association between TNF-ɑ-308G/A polymorphism and esophageal cancer risk: An updated meta-analysis and trial sequential analysis.

作者信息

Yang Fengming, Wei Ke, Qin Zhiqiang, Shao Chuchu, Shu Yongqian, Shen Hua

机构信息

Department of Oncology, The Affiliated Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu Province, China.

Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu Province,China.

出版信息

J Cancer. 2019 Jan 29;10(5):1086-1096. doi: 10.7150/jca.29390. eCollection 2019.

Abstract

: TNF-α-308G/A (rs1800629) polymorphism has been previously implicated in the susceptibility to esophageal cancer, but results of these studies remained controversial or ambiguous. A meta-analysis was conducted to provide a more reliable conclusion about the association between TNF-ɑ-308G/A polymorphism and risk of esophageal cancer. : Databases such as PubMed, EMBASE, Web of Science and CNKI were searched for relevant articles published till June 1, 2018. We used the pooled odds ratios (ORs) with 95% confidence intervals (CIs) to evaluate the strength of such associations. Subgroup analysis was carried out according to ethnicity, source of controls and genotyping method. A trial sequential analysis (TSA) was performed to reduce the risk of type I error and evaluate whether the results of our meta-analysis were credible. : A total of 9 published case-control studies with 1,435 esophageal cancer patients and 3,762 healthy controls were identified. Overall, our results indicated no significant correlation between TNF-α-308G/A polymorphism and increased risk of esophageal cancer in the fixed-effects model (: pooled OR=1.11, 95% CI: 0.96-1.27, : pooled OR=1.23, 95% CI: 0.77-1.95, : pooled OR=1.14, 95% CI: 0.97-1.35, : pooled OR=1.14, 95% CI: 0.97-1.34 and : pooled OR=1.00, 95% CI: 0.64-1.56). Subgroup analysis by ethnicity, source of controls and genotyping method showed no significant increase in the risk of esophageal cancer. TSA results need further investigation with a large sample size to certify such association. : This meta-analysis study suggested no significant association between TNF-ɑ-308G/A polymorphism and the risk of esophageal cancer.

摘要

肿瘤坏死因子-α-308G/A(rs1800629)多态性先前已被认为与食管癌易感性有关,但这些研究结果仍存在争议或不明确。进行了一项荟萃分析,以得出关于肿瘤坏死因子-α-308G/A多态性与食管癌风险之间关联的更可靠结论。在PubMed、EMBASE、科学网和中国知网等数据库中检索截至2018年6月1日发表的相关文章。我们使用合并比值比(OR)及95%置信区间(CI)来评估这种关联的强度。根据种族、对照来源和基因分型方法进行亚组分析。进行了一项试验序贯分析(TSA)以降低I类错误风险,并评估我们荟萃分析的结果是否可信。共纳入9项已发表的病例对照研究,包括1435例食管癌患者和3762例健康对照。总体而言,我们的结果表明,在固定效应模型中,肿瘤坏死因子-α-308G/A多态性与食管癌风险增加之间无显著相关性(合并OR=1.11,95%CI:0.96-1.27;合并OR=1.23,95%CI:0.77-1.95;合并OR=1.14,95%CI:0.97-1.35;合并OR=1.14,95%CI:0.97-1.34;合并OR=1.00,95%CI:0.64-1.56)。按种族、对照来源和基因分型方法进行的亚组分析显示,食管癌风险无显著增加。TSA结果需要通过大样本量进一步研究以证实这种关联。这项荟萃分析研究表明,肿瘤坏死因子-α-308G/A多态性与食管癌风险之间无显著关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f45f/6400664/d838c33ddec7/jcav10p1086g001.jpg

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