Meta-Analysis-Based Preliminary Exploration of the Connection between ATDILI and Schizophrenia by GSTM1/T1 Gene Polymorphisms

被引:13
作者
Cai, Lei [1 ,2 ]
Cai, Mei-Hong [3 ]
Wang, Mei-Yan [4 ]
Xu, Yi-Feng [1 ,2 ]
Chen, Wen-Zhong [2 ]
Qin, Shen-Ying [1 ,2 ]
Wan, Chun-Ling [1 ,2 ]
He, Lin [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Minist Educ, Bio X Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Shanghai 200030, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Mental Hlth Ctr, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Shanghai 200020, Peoples R China
[4] Tongji Univ, Sch Life Sci & Technol, Shanghai 200092, Peoples R China
基金
美国国家科学基金会;
关键词
DRUG-INDUCED HEPATOTOXICITY; GLUTATHIONE S-TRANSFERASES; ANTITUBERCULOSIS DRUGS; TISSUE DISTRIBUTION; SUSCEPTIBILITY; METAANALYSIS; GSTT1; LIVER; IDENTIFICATION; ASSOCIATIONS;
D O I
10.1371/journal.pone.0128643
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Anti-tuberculosis drugs have some adverse effects such as anti-tuberculosis drug-induced liver injury (ATDILI) and mental disorders. The involvement of glutathione S-transferase (GST) genes in pathogenesis of ATDILI or schizophrenia (SCZ) has been reported. Therefore, GST genes may exemplify molecular connectors between ATDILI and SCZ. However, association studies of GSTM1/T1 polymorphisms with these two diseases have yielded conflicting results. After searching case-control association studies in PubMed, ISI Web of Science, EMBASE, Chinese National Knowledge Infrastructure (CNKI), and Chinese BioMedical Literature Database, we performed meta-analyses across a total of 20 published association studies on 3146 subjects for the association of GSTM1 and ATDILI, 2587 for the GSTT1-ATDILI association, 2283 for GSTM1-SCZ and 1116 for GSTT1-SCZ to test the associations of GSTM1/T1 polymorphisms with ATDILI and SCZ. The GSTM1 present genotype was significantly associated with decreased risks of ATDILI (risk ratio(RR): 0.81, 95% confidence interval (CI): 0.75-0.88, P < 0.0001) and SCZ (RR: 0.88, 95% CI: 0.80-0.96, P = 0.004) according to the fixed-effect model, while the GSTT1 present genotype was significantly associated only with a high risk of SCZ (RR: 1.17, 95% CI: 1.04-1.32, P = 0.01) according to both the random- and fixed-effect models, but not with ATDILI (P = 0.82) according to the fixed-effect model. Moreover, these significant results were supported with moderate evidence according to the Venice criteria. These results indicate that GSTM1 represents a genetic connection between ATDILI and SCZ, and suggest that ATDILI and SCZ may be co-occurring for the subjects with GSTM1 null genotype.
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页数:12
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