LAUSR

Abstract Reports of the role of host interleukin 28B (IL-28B) genetic variants in liver disease severity in patients with chronic hepatitis C (CHC) have obtained conflicting results. The impact of IL-28B in Asian patients with different viral genotypes remains elusive. We try to elucidate the effect of IL-28B genetic variants in a large Asian cohort with different viral genotypes. The association between the IL-28B rs8099917 genotype and liver fibrosis was investigated in 1288 patients with biopsy-proven CHC. Patients with hepatitis C virus genotype 1 (HCV-1) infection comprised 59.4% of the population. The remaining 40.6% (518 patients) did not have HCV-1 infection. Of the 1084 patients with the IL-28 genotype, 85.6% (928 patients) had the TT genotype. Univariate analysis revealed that, compared to patients without advanced liver fibrosis, patients with advanced liver fibrosis (Metavir fibrosis score 3–4) had an older age, a lower platelet count, a higher &agr;-fetoprotein level, a higher alanine aminotransferase level, a higher incidence of diabetes, and a higher frequency of rs8099917 non-TT genotype carriage. Logistic regression analysis revealed that factors significantly associated with advanced liver fibrosis included age (odds ratio [OR]/95% confidence interval [CI]: 1.023/1.009–1.037, P = .001), diabetes (OR/CI: 1.736/1.187–2.539, P = .004), &agr;-fetoprotein (OR/CI: 1.007/1.002–1.012, P = .009), platelet count (OR/CI: 0.991/0.988–0.993, P < .001), and carriage of the rs8099917 non-TT genotype (OR/CI: 0.585/0.400–0.856, P = .006). When patients were classified by viral genotype, factors that had significant independent associations with advanced liver fibrosis in patients with HCV-1 infection included diabetes (OR/CI: 2.379/1.452–3.896, P = .001), &agr;-fetoprotein (OR/CI: 1.023/1.012–1.035, P < .001), platelet count (OR/CI: 0.99/0.987–0.994, P < .001), and carriage of the rs8099917 non-TT genotype (OR/CI: 0.529/0.328–0.854, P = .009). In patients who had advanced liver fibrosis but not HCV-1 infection, factors that had significant independent associations with advanced liver fibrosis included age (OR/CI: 1.039/1.016–1.063, P = .001) and platelet count (OR/CI: 0.99/0.986–0.995, P < .001); additionally, IL-28B genetic variants were not associated with liver disease severity. Unfavorable IL-28B genetic variants were associated with advanced liver disease. The genetic effect is limited to patients with HCV-1 infection.