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谷胱甘肽硫转移酶 M1 缺失基因型与喉癌风险的关联的定量评估。

Quantitative assessment of the association between GSTM1 null genotype and laryngeal cancer risk.

机构信息

Department of Otolaryngology Head and Neck Surgery, The Second Affiliated Hospital of Harbin Medical University, 246 Xue Fu Road, Harbin 150081, China.

出版信息

Eur Arch Otorhinolaryngol. 2013 Feb;270(2):615-22. doi: 10.1007/s00405-012-2148-7. Epub 2012 Sep 13.

Abstract

Previous studies investigating the association between glutathione S-transferase M1 (GSTM1) null genotype and laryngeal cancer risk reported controversial results. Thus, a meta-analysis was performed to clarify the effect of GSTM1 null genotype on laryngeal cancer risk. A literature search was performed for all possible studies. We estimated summary odd ratio (OR) with its 95 % confidence interval (95 % CI) to assess the association. Subgroup analyses were performed by ethnicity or the sample size. 24 individual case-control studies involving a total of 2,809 laryngeal cancer cases and 4,478 controls were finally included into this meta-analysis. Meta-analyses of total 24 studies showed the GSTM1 null genotype was significantly associated with increased laryngeal cancer risk (random-effects OR = 1.44, 95 % CI 1.19-1.73, P < 0.001). Subgroup analyses by ethnicity showed that the GSTM1 null genotype was associated with increased laryngeal cancer risk in both Caucasians (fixed-effects OR = 1.17, 95 % CI 1.04-1.33, P = 0.012) and Asians (random-effects OR = 1.89, 95 % CI 1.28-2.77, P = 0.001). Also, subgroup analyses by sample size also further identified this association above. The cumulative meta-analyses showed a trend of more obvious association between GSTM1 null genotype and increased risk of laryngeal cancer as information accumulated by year. Meta-analysis of available data suggests that GSTM1 null genotype contributes to increased laryngeal cancer risk in both Caucasians and East Asians.

摘要

先前研究 GST 转移酶 M1(GSTM1)无效基因型与喉癌风险之间的关系,结果存在争议。因此,进行荟萃分析以阐明 GSTM1 无效基因型对喉癌风险的影响。对所有可能的研究进行文献检索。我们使用汇总比值比(OR)及其 95%置信区间(95%CI)来评估关联。按种族或样本量进行亚组分析。最终纳入了 24 项个体病例对照研究,共涉及 2809 例喉癌病例和 4478 例对照。24 项研究的荟萃分析表明,GSTM1 无效基因型与喉癌风险增加显著相关(随机效应 OR = 1.44,95%CI 1.19-1.73,P <0.001)。按种族进行的亚组分析表明,GSTM1 无效基因型与白种人(固定效应 OR = 1.17,95%CI 1.04-1.33,P = 0.012)和亚洲人(随机效应 OR = 1.89,95%CI 1.28-2.77,P = 0.001)的喉癌风险增加均相关。此外,按样本量进行的亚组分析也进一步证实了这种关联。累积荟萃分析表明,随着年份信息的积累,GSTM1 无效基因型与喉癌风险增加之间的关联趋势更为明显。现有数据的荟萃分析表明,GSTM1 无效基因型在白种人和东亚人群中均导致喉癌风险增加。

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