Suppr超能文献

谷胱甘肽 S-转移酶 M1 和 T1 缺失多态性与抗结核药物性肝损伤易感性的关系:一项荟萃分析。

GSTM1 and GSTT1 null polymorphisms and susceptibility to anti-tuberculosis drug-induced liver injury: a meta-analysis.

机构信息

Department of General Toxicology, National Shanghai Center for New Drug Safety Evaluation and Research, Shanghai Institute of Pharmaceutical Industry, Shanghai, China.

出版信息

Int J Tuberc Lung Dis. 2013 Jan;17(1):17-25. doi: 10.5588/ijtld.12.0447.

Abstract

BACKGROUND

Published data on the association between GSTM1 and GSTT1 polymorphisms and risk of anti-tuberculosis drug-induced liver injury (ATDILI) are inconclusive.

OBJECTIVE

To derive a more precise estimation of the relationship, a meta-analysis on this topic was performed.

DESIGN

PubMed, Medline, EMBASE and Chinese national knowledge infrastructure were searched for studies on the association of GSTM1 and GSTT1 polymorphisms with risk of ATDILI. Summary odds ratios (ORs) with their corresponding 95% confidence intervals (CIs) were calculated.

RESULTS

The GSTM1 null genotype was associated with increased risk of ATDILI (OR(random-effects) 1.50, 95%CI 1.15-1.95). When stratifying for study population and median number of cases, statistically significant results were observed in the Chinese population (OR(random-effects) 1.45, 95%CI 1.12-1.92) and in studies with case numbers > 57 (OR(fixed-effects) 1.60, 95%CI 1.31-1.97). No statistically significant association was observed between GSTT1 null genotype or GSTM1/GSTT1 interaction and risk of ATDILI.

CONCLUSION

The meta-analysis suggests that GSTM1 null genotype may be associated with an increased risk of ATDILI, particularly among the Chinese population. The GSTT1 null genotype or GSTM1/GSTT1 interaction may not affect susceptibility to ATDILI.

摘要

背景

关于 GSTM1 和 GSTT1 多态性与抗结核药物性肝损伤(ATDILI)风险之间的关联,已有发表的数据尚无定论。

目的

通过荟萃分析对这一主题进行研究,以获得更准确的评估。

设计

检索了关于 GSTM1 和 GSTT1 多态性与 ATDILI 风险之间关联的研究,检索数据库包括 PubMed、Medline、EMBASE 和中国国家知识基础设施。计算了汇总优势比(OR)及其相应的 95%置信区间(CI)。

结果

GSTM1 缺失基因型与 ATDILI 风险增加相关(随机效应汇总 OR 1.50,95%CI 1.15-1.95)。在按研究人群和中位数病例数进行分层时,在中国人群中观察到统计学显著的结果(随机效应汇总 OR 1.45,95%CI 1.12-1.92),且在病例数>57 的研究中观察到统计学显著的结果(固定效应汇总 OR 1.60,95%CI 1.31-1.97)。GSTT1 缺失基因型或 GSTM1/GSTT1 相互作用与 ATDILI 风险之间无统计学显著关联。

结论

荟萃分析表明,GSTM1 缺失基因型可能与 ATDILI 风险增加相关,尤其是在中国人群中。GSTT1 缺失基因型或 GSTM1/GSTT1 相互作用可能不会影响 ATDILI 的易感性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验