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MTHFR C677T Gene Polymorphism and Head and Neck Cancer Risk: A Meta-Analysis Based on 23 Publications

机译:MTHFR C677T基因多态性与头颈癌风险:基于23种出版物的荟萃分析

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摘要

Objective. Conflicting results on the association between MTHFR polymorphism and head and neck cancer (HNC) risk were reported. We therefore performed a meta-analysis to derive a more precise relationship between MTHFR C677T polymorphism and HNC risk. Methods. Three online databases of PubMed, Embase, and CNKI were researched on the associations between MTHFR C677T polymorphism and HNC risk. Twenty-three published case-control studies involving 4,955 cases and 8,805 controls were collected. Odds ratios (ORs) with 95% confidence interval (CI) were used to evaluate the relationship between MTHFR C677T polymorphism and HNC risk. Sensitivity analysis, cumulative analyses, and publication bias were conducted to validate the strength of the results. Results. Overall, no significant association between MTHFR C677T polymorphism and HNC risk was found in this meta-analysis (T versus C: OR = 1.04, 95% CI = 0.92–1.18; TT versus CC: OR = 1.15, 95% CI = 0.90–1.46; CT versus CC: OR = 1.00, 95% CI = 0.85–1.17; CT + TT versus CC: OR = 1.01, 95% CI = 0.87–1.18; TT versus CC + CT: OR = 1.11, 95% CI = 0.98–1.26). In the subgroup analysis by HWE, ethnicity, study design, cancer location, and negative significant associations were detected in almost all genetic models, except for few significant risks that were found in thyroid cancer. Conclusion. This meta-analysis demonstrates that MTHFR C677T polymorphism may not be a risk factor for the developing of HNC.
机译:目的。据报道,MTHFR基因多态性与头颈癌(HNC)风险之间存在关联性冲突的结果。因此,我们进行了荟萃分析,以得出MTHFR C677T多态性与HNC风险之间更精确的关系。方法。研究了三个在线PubMed,Embase和CNKI数据库,以研究MTHFR C677T多态性与HNC风险之间的关系。收集了23份涉及4955例病例和8805例对照的已发表病例对照研究。具有95%置信区间(CI)的比值比(OR)用于评估MTHFR C677T多态性与HNC风险之间的关系。进行敏感性分析,累积分析和出版偏倚以验证结果的强度。结果。总体而言,在该荟萃分析中未发现MTHFR C677T多态性与HNC风险之间存在显着关联(T与C:OR = 1.04,95%CI = 0.92-1.18; TT与CC:OR = 1.15,95%CI = 0.90– 1.46; CT与CC:OR = 1.00,95%CI = 0.85-1.17; CT + TT与CC:OR = 1.01,95%CI = 0.87-1.18; TT与CC + CT:OR = 1.11,95%CI = 0.98–1.26)。在HWE进行的亚组分析中,除了少数在甲状腺癌中发现的重大风险外,几乎所有的遗传模型中都检测到了种族,研究设计,癌症位置和负显着关联。结论。这项荟萃分析表明,MTHFR C677T多态性可能不是HNC发生的危险因素。

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