The role of viral and host genetics in natural history and treatment of chronic HCV infection

被引:23
|
作者
Doyle, Joseph S. [1 ,2 ,3 ]
Hellard, Margaret E. [1 ,2 ,3 ]
Thompson, Alexander J. [4 ,5 ,6 ,7 ]
机构
[1] Burnet Inst, Ctr Populat Hlth, Melbourne, Vic 3004, Australia
[2] Alfred Hosp, Infect Dis Unit, Melbourne, Vic, Australia
[3] Monash Univ, Dept Epidemiol & Preventat Med, Melbourne, Vic 3004, Australia
[4] St Vincents Hosp, Dept Gastroenterol & Hepatol, Melbourne, Vic 3065, Australia
[5] Victorian Infect Dis Reference Lab, Melbourne, Vic, Australia
[6] Duke Univ, Med Ctr, Duke Clin Res Inst, Durham, NC USA
[7] Duke Univ, Med Ctr, Dept Gastroenterol, Durham, NC USA
基金
英国医学研究理事会;
关键词
Hepatitis C virus; Genetics; Genome-wide association; Natural history; Treatment; IL28B; Single nucleotide polymorphism; HEPATITIS-C VIRUS; SUSTAINED VIROLOGICAL RESPONSE; GENOME-WIDE-ASSOCIATION; LIVER FIBROSIS PROGRESSION; INTERFERON-FREE REGIMEN; SENSITIVITY-DETERMINING REGION; INHIBITORY RECEPTOR GENES; TREATMENT-NAIVE PATIENTS; AMINO-ACID SUBSTITUTION; CIRRHOSIS RISK SCORE;
D O I
10.1016/j.bpg.2012.09.004
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Understanding of the natural history and treatment responsiveness of chronic hepatitis C virus (HCV) infection has evolved rapidly in recent years. Advances in HCV molecular virology and host genetics can now better predict spontaneous clearance and treatment outcomes. HCV genotype is the most important viral factor predicting interferon-alpha treatment responsiveness; HCV-1 subtype is emerging as a key determinant of the efficacy of direct acting antiviral therapy. Genome-wide association studies have recently identified several clinically important host determinants of the outcomes of peginterferon-alpha and ribavirin treatment outcome: IL28B polymorphism is associated with spontaneous clearance and treatment responsiveness; ITPA polymorphism protects against ribavirin-induced anaemia and dose reductions; genetic determinants of liver fibrosis progression rate have been proposed. In this review, we evaluate the role of viral and host genetics in the natural history and treatment outcomes of chronic HCV infection, and consider how this knowledge might help individualize clinical management in the era of DAA therapy. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:413 / 427
页数:15
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