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Effects of fatty liver and related factors on the efficacy of combination antiviral therapy in patients with chronic hepatitis C
Author(s) -
Jian Wu Yu,
Shu Chen Li,
Gui Qiang Wang
Publication year - 2006
Publication title -
liver international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.873
H-Index - 110
eISSN - 1478-3231
pISSN - 1478-3223
DOI - 10.1111/j.1478-3231.2005.01219.x
Subject(s) - medicine , ribavirin , fatty liver , gastroenterology , insulin resistance , steatosis , genotype , hepatitis c virus , body mass index , combination therapy , hepatitis c , insulin , immunology , biology , virus , biochemistry , disease , gene
Objective: Hepatic steatosis is a histological feature in patients with chronic hepatitis C (CHC) and adversely affects the virologic response rates to anti‐hepatitis C virus (HCV) therapy. The aim of this study is to investigate whether the fatty liver and related factors have impact on the efficacy in CHC treated with peginterferon and ribavirin, and the associations between HCV genotyping and fatty liver. Methods: Ninety‐eight patients received subcutaneously 180 μg peginterferon α‐2a once a week plus ribavirin. HCV genotypes and the levels of plasma insulin of patients were measured. Fatty liver was detected by B ultrasound. The body mass index (BMI), waist‐to‐hip ratio (WHR) and homeostasis model assessment of insulin resistance (HOMA‐IR) were calculated. Results: Among 98 CHC patients, 38 (38.8%) were infected with genotype 1; 44 (44.9%) with genotype 2; 13 (13.3%) with genotype 3; 3 (3.0%) with indeterminate genotype. The prevalence of fatty liver was 10.5%, 11.4%, 38.5% in patients infected with HCV genotype 1, 2, 3, respectively, which suggested that the distribution of fatty liver in different HCV genotypes was imbalanced (χ 2 =6.758, P =0.034). In univariate analysis, the efficacy of combination therapy was significantly associated with BMI ( P =0.011), WHR ( P =0.024), the levels of plasma insulin ( P =0.001), genotype ( P =0.036), presence of fatty liver ( P =0.028), treatment dosage and duration ( P =0.012) and HOMA‐IR ( P =0.002). With binary logistic regression analysis, the plasma insulin levels and HOMA‐IR showed independent predictors to the efficacy of antiviral therapy. Conclusion: The prevalence of fatty liver in HCV genotype 3 was markedly higher than that of other genotypes. The BMI, WHR, the levels of plasma insulin, genotype, presence of fatty liver, treatment dosage and duration and HOMA‐IR were associated with the sustained virologic response. The level of plasma insulin and HOMA‐IR were independent factors for predicting effect of antiviral therapy.