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首页> 外文期刊>Medicine. >Does CYP2E1 RsaI/PstI polymorphism confer head and neck carcinoma susceptibility?: A meta-analysis based on 43 studies
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Does CYP2E1 RsaI/PstI polymorphism confer head and neck carcinoma susceptibility?: A meta-analysis based on 43 studies

机译:CYP2E1 RsaI / PstI基因多态性是否赋予头颈癌易感性:基于43项研究的荟萃分析

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Background:Previous reports showed that CYP2E1RsaI/PstI polymorphism may be a risk factor for cancers. Published meta-analyses in 2010 and 2011, respectively, on the relationship of CYP2E1RsaI/PstI polymorphisms with the susceptibility to head and neck carcinoma (HNC) have generated inconsistent results. Thus, this study aimed to conduct an updated meta-analysis involving published studies up to Nov 2015 to get a more confidential result.Methods:Eligible studies up to Nov 2015 were retrieved and screened. Data were extracted and a quantitative meta-analysis was conducted. Subgroup analyses on ethnicity, source of controls, sample size, genotyping method, smoking status, and drinking status were also performed.Results:Forty-one publications including a total of 43 case-control studies were selected for analysis. The overall data under a homozygote comparison model indicated a significant association of CYP2E1RsaI/PstI polymorphisms with HNC risk (c2c2 vs c1c1: odds ratio [OR] = 1.97; 95% confidence interval [CI] = 1.53-2.53). Similar results were observed in the Asian subgroup (c2c2 vs c1c1: OR = 1.98; 95%CI = 1.51-2.60; c2 vs c1: OR = 1.20; 95%CI = 1.03-1.39) and mixed population (c2 vs c1: OR = 1.41; 95%CI = 1.06-1.86) when the data were stratified by ethnicities. Interestingly, increased cancer risk only was shown among never-smokers (c2c2+c1c2 vs c1c1: OR = 1.44; 95%CI = 1.05-1.98) but not ever-smokers.Conclusion:CYP2E1RsaI/PstI polymorphisms may modify the susceptibility to HNC, particularly among Asians, mixed population, and never-smokers. Future large and well-designed studies are needed to verify this conclusion.
机译:背景:以前的报道表明CYP2E1RsaI / PstI多态性可能是癌症的危险因素。分别在2010年和2011年发表的关于CYP2E1RsaI / PstI多态性与头颈癌(HNC)敏感性关系的荟萃分析产生了不一致的结果。因此,本研究旨在进行更新的荟萃分析,涉及截至2015年11月的已发表研究,以获得更机密的结果。方法:检索并筛选截至2015年11月的合格研究。提取数据并进行定量荟萃分析。结果:选择了41篇出版物,包括43项病例对照研究,进行了种族,控制源,样本量,基因分型方法,吸烟状况和饮酒状况的亚组分析。纯合子比较模型下的总体数据表明CYP2E1RsaI / PstI多态性与HNC风险显着相关(c2c2 vs c1c1:优势比[OR] = 1.97; 95%置信区间[CI] = 1.53-2.53)。在亚洲亚组(c2c2 vs c1c1:OR = 1.98; 95%CI = 1.51-2.60; c2 vs c1:OR = 1.20; 95%CI = 1.03-1.39)和混合人群(c2 vs c1:OR)中也观察到了相似的结果= 1.41; 95%CI = 1.06-1.86)。有趣的是,仅从未吸烟者(c2c2 + c1c2 vs c1c1:OR = 1.44; 95%CI = 1.05-1.98)中显示出患癌风险增加,但从未吸烟者中发现。结论:CYP2E1RsaI / PstI多态性可能会改变对HNC的易感性,特别是在亚洲人,混血人口和不吸烟者中。需要未来的大型且设计良好的研究来验证该结论。

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