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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Lack of association between glutathione S-transferase T1 gene polymorphism and laryngeal cancer susceptibility: A meta-analysis based on 2,124 cases and 2,059 controls
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Lack of association between glutathione S-transferase T1 gene polymorphism and laryngeal cancer susceptibility: A meta-analysis based on 2,124 cases and 2,059 controls

机译:谷胱甘肽S-转移酶T1基因多态性和喉癌易感性之间缺乏关联:基于2,124例和2,059例控制的Meta分析

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摘要

Studies investigating the association between glutathione S-transferase T1 (GSTT1) gene polymorphism and laryngeal cancer susceptibility have reported conflicting results. The aim of the present study was to conduct a meta-analysis assessing the possible association of GSTT1 gene polymorphism with laryngeal cancer risk. The relevant studies were identified through a search of PubMed, Embase, ISI Web of Knowledge and Chinese National Knowledge Infrastructure until May 2011. Twelve studies were included in the present meta-analysis, which described a total of 2124 laryngeal cancer cases and 2059 controls. The overall odds ratio (OR) for GSTT1 null genotype was 1.40 (95% CI = 0.90-2.16). When stratifying for race, the pooled ORs for GSTT1 null genotype were 1.07 (95% CI = 0.81-1.41) in Caucasians and 5.63 (95% CI = 1.00-31.83) in Asians. The pooled ORs for GSTT1 null genotype were 1.03 (95% CI = 0.71-1.49) in population-based studies and 2.39 (95% CI = 0.73-7.86) in hospital-based studies, stratifying for study design. This meta-analysis suggested that there was lack of association between GSTT1 gene polymorphism and laryngeal cancer risk. However, larger scale primary studies are still required to further evaluate the interaction of GSTT1 gene polymorphism with laryngeal cancer risk.
机译:研究谷胱甘肽S-转移酶T1(GSTT1)基因多态性和喉癌易感性之间的研究报告了突破性的结果。本研究的目的是进行荟萃分析,评估GSTT1基因多态性与喉癌风险的可能关联。通过搜索知识和中国国家知识基础设施的PUBMED,EMBASE,ISI网络,直到2011年5月,确定了相关研究。本次数分析中包括12项研究,该研究总共描述了2124例喉癌病例和2059例。 GSTT1 null基因型的总体差值(或)为1.40(95%Ci = 0.90-2.16)。当对种族分层时,Caucasians的GSTT1 Null基因型的合并或用于GSTT1 Null基因型的汇总或者在亚洲人的5.63(95%CI = 1.00-31.83)中为1.07(95%CI = 0.81-1.41)。基于人群的研究和2.39(95%CI = 0.71-1.49)的GSTT1 null基因型为1.03(95%CI = 0.71-1.49),在医院的研究中进行2.39(95%CI = 0.73-7.86),用于研究设计。该META分析表明GSTT1基因多态性和喉癌风险之间缺乏关联。然而,仍然需要大规模的初步研究以进一步评估GSTT1基因多态性与喉癌风险的相互作用。

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