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谷胱甘肽S-转移酶M1基因缺失型对儿童急性白血病风险的影响:一项荟萃分析。

Effect of GSTM1 null genotype on risk of childhood acute leukemia: a meta-analysis.

作者信息

Ma Yan, Sui Yun, Wang Lizhen, Li Huirong

出版信息

Tumour Biol. 2014 Jan;35(1):397-402. doi: 10.1007/s13277-013-1055-x.

Abstract

Glutathione S-transferases are important enzymes in the detoxification of a wide range of reactive oxygen species. Recently, there have been a number of studies on the association between Glutathione S-transferase M1 (GSTM1) null genotype and childhood acute leukemia in Chinese, but the results of previous reports are inconsistent. Thus, we performed a meta-analysis to clarify the effect of GSTM1 null genotype on childhood acute leukemia risk. PubMed, Embase, and Wanfang databases were searched to identify case–control studies investigating the association between GSTM1 null genotype and risk of childhood acute leukemia. Between-study heterogeneity was assessed using the I2 statistic method. Odds ratios (OR) with corresponding 95% confidence intervals (95% CI) were pooled to assess the association. Seven case–control studies were finally included in the meta-analysis. There was no between-study heterogeneity among those seven studies (I2 = 0%). Overall, the GSTM1 null genotype was significantly associated with increased risk of childhood acute leukemia in Chinese (fixed effect OR = 2.49; 95% CI, 1.84–3.37; P < 0.001). The cumulative meta-analyses showed a trend of more obvious association between GSTM1 null genotype and risk of childhood acute leukemia in Chinese as data accumulated by year. Sensitivity analysis by omitting single study in turns also did not materially alter the pooled ORs. Therefore, the GSTM1 null genotype is significantly associated with increased risk of childhood acute leukemia in Chinese.

摘要

谷胱甘肽S-转移酶是广泛的活性氧解毒过程中的重要酶。最近,关于谷胱甘肽S-转移酶M1(GSTM1)基因缺失型与中国儿童急性白血病之间的关联已有多项研究,但先前报告的结果并不一致。因此,我们进行了一项荟萃分析,以阐明GSTM1基因缺失型对儿童急性白血病风险的影响。检索了PubMed、Embase和万方数据库,以确定调查GSTM1基因缺失型与儿童急性白血病风险之间关联的病例对照研究。采用I2统计方法评估研究间的异质性。汇总比值比(OR)及其相应的95%置信区间(95%CI)以评估关联性。最终有7项病例对照研究纳入了荟萃分析。这7项研究之间不存在研究间异质性(I2 = 0%)。总体而言,在中国,GSTM1基因缺失型与儿童急性白血病风险增加显著相关(固定效应OR = 2.49;95%CI,1.84 - 3.37;P < 0.001)。累积荟萃分析显示,随着逐年积累的数据,在中国,GSTM1基因缺失型与儿童急性白血病风险之间的关联有更明显的趋势。依次剔除单项研究的敏感性分析也未实质性改变汇总的OR值。因此,在中国,GSTM1基因缺失型与儿童急性白血病风险增加显著相关。

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