GSTM1 and GSTT1 genetic polymorphisms and their association with antituberculosis drug-induced liver injury

被引:15
作者
Chanhom, Noppadol [1 ]
Udomsinprasert, Wanvisa [1 ]
Chaikledkaew, Usa [2 ]
Mahasirimongkol, Surakameth [3 ]
Wattanapokayakit, Sukanya [3 ]
Jittikoon, Jiraphun [1 ]
机构
[1] Mahidol Univ, Fac Pharm, Dept Biochem, 447 Sri Ayuthaya Rd, Bangkok 10400, Thailand
[2] Mahidol Univ, Fac Pharm, Dept Pharm, Bangkok 10400, Thailand
[3] Minist Publ Hlth, Dept Med Sci, Genom Med Ctr, Div Genom Med & Innovat Support, Nonthaburi 11000, Thailand
关键词
drug-induced liver injury; glutathione S-transferase; tuberculosis; hepatotoxicity; systematic review; meta-analysis; adverse effect; genetic polymorphisms; S-TRANSFERASE M1; INDUCED HEPATOTOXICITY; OXIDATIVE STRESS; NULL MUTATIONS; CYP2E1; SUSCEPTIBILITY; GENOTYPES; RISK; NAT2; T1;
D O I
10.3892/br.2020.1275
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Antituberculosis (anti-TB) drugs are the most common cause of drug-induced liver injury (DILI). There are numerous studies revealing the associations between the polymorphisms of pharmacogenes and the risk of anti-TB DILI (ATDILI). In the present study, relevant studies regarding the pharmacogenes associated with ATDILI were systematically searched in PubMed and Scopus. A total of 24 genes associated with ATDILI were reported on and the top five reported genes in terms of frequency were revealed to be N-acetyltransferase 2, cytochrome P450 family 2 subfamily E member 1, glutathione S-transferases [glutathione S-transferase mu 1 (GSTM1) and glutathione S-transferase theta 1 (GSTT1)] and solute carrier organic anion transporter family member 1B1. As ATDILI may be the result of direct and indirect interactions, the encoded proteins were further analysed using the Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) to observe the protein-protein interactions and the associations amongst these proteins. The results suggested that only GSTT1 and GSTM1 were central proteins associated with all the other analysed proteins. Therefore, the association between GSTT1 or GSTM1 and the risk of developing ATDILI were further analysed. The results revealed that a GSTM1 deletion genotype was significantly associated with risk of ATDILI [odds ratio (OR), 1.28; 95% confidence interval (CI), 1.08-1.51; P=0.004], whereas the GSTT1 deletion genotype and GSTM1/GSTT1 dual-deletion genotype were not significantly associated with risk of ATDILI. Subgroup analysis based on ethnicity was performed and the results demonstrated a significant association between GSTM1 and ATDILI in South Asian individuals (OR, 1.48; 95% CI, 1.12-1.95; P=0.005), which has not been reported previously, to the best of our knowledge. In conclusion, GSTM1 was associated with ATDILI in South Asian individuals.
引用
收藏
页码:153 / 162
页数:10
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