GSTT1 and GSTM1 null genotypes may facilitate hepatitis C virus infection becoming chronic

被引:16
作者
Martinez, Carmen
Garcia-Martin, Elena
Ladero, Jose M.
Herraez, Oscar
Ortega, Luis
Taxonera, Carlos
Suarez, Avelina
Diaz-Rubio, Manuel
Agundez, Jose A. G.
机构
[1] Univ Complutense Madrid, Liver Unit, Gastroenterol Serv, Hosp Clin San Carlos, Madrid 28040, Spain
[2] Univ Complutense Madrid, Serv Pathol, Hosp Clin San Carlos, Madrid 28040, Spain
[3] Univ Complutense Madrid, Microbiol Serv, Hosp Clin San Carlos, Madrid 28040, Spain
[4] Univ Extremadura, Dept Pharmacol & Psychiat, Badajoz, Spain
[5] Univ Extremadura, Dept Biochem, Badajoz, Spain
[6] Univ Extremadura, Dept Mol Biol, Badajoz, Spain
[7] Univ Extremadura, Dept Genet, Badajoz, Spain
关键词
D O I
10.1086/513569
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Oxidative stress contributes to hepatitis C virus (HCV)-induced liver damage. The activity of antioxidant glutathione S-transferases (GSTs) T1 and M1 is polymorphic. The GSTT1 and GSTM1 genotypes were identified in 139 HCV-infected patients and in 329 healthy individuals. Among patients, there was an excess of GSTT1 (odds ratio [OR], 2.76 [95%confidence interval {CI}, 1.77 - 4.30]; P < .001) and GSTM1 (OR, 1.54 [95% CI, 1.02 - 2.35];) null genotypes and of double-null haplotypes (OR, 3.65 [95% CI, 1.98 - 6.75];). The GSTT1 null genotype, particularly if associated P < .001 with the GSTM1 null genotype, may facilitate HCV infection becoming chronic.
引用
收藏
页码:1320 / 1323
页数:4
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