Vitamin D and
vitamin D receptor (VDR) are involved in multiple immune-mediated disorders including
chronic hepatitis C virus (HCV)
infection. The aim of this study was to determine the association between plasma
vitamin D level, VDR genetic polymorphisms and risk of HCV
infection susceptibility and chronicity. Seven single nucleotide polymorphisms (SNPs) in VDR gene were genotyped and plasma
25-hydroxyvitamin D [25(
OH)D] levels were measured in a Han Chinese population of 898 HCV
persistent infection cases, 558 spontaneous clearance subjects and 1136 uninfected controls with high risk of HCV
infection. In this case-control study, the average plasma 25(
OH)D level in
persistent infection patients was significantly lower than that in spontaneous clearance cases (P=0.039) and controls (P=0.005). Logistic analyses indicated that rs7975232-C, rs2239185-T and rs11574129-T alleles were significantly associated with a decreased risk of HCV
infection susceptibility (all PBonferroni<0.05, in additive/dominant models; Ptrend=9.000×10(-4), combined effects in a locus-dosage manner). The protective effects of three favorable alleles were more evident among males, females and subjects aged ≤50years (all P<0.05). Haplotype analyses suggested that compared with the most frequent haplotype Ars7975232Trs731236Crs11574129, CTT was correlated with a reduced risk of HCV
infection susceptibility (
P=2.200×10(-3)). These findings implied that low
vitamin D levels might be associated with an increased risk for HCV
infection and chronicity, and favorable VDR variants (rs7975232-C, rs2239185-T and rs11574129-T) might contribute to a decreased susceptibility to HCV
infection in a high-risk Chinese population.