Department of Otolaryngology Head and Neck Surgery, The Second Affiliated Hospital of Harbin Medical University, 246 Xue Fu Road, Harbin 150081, China.
Eur Arch Otorhinolaryngol. 2013 Feb;270(2):615-22. doi: 10.1007/s00405-012-2148-7. Epub 2012 Sep 13.
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.
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。