Abstract

BackgroundTo explore associations between PON1 rs854560, rs662, 705,379, HCV clearance, and interactions between tested PON1 single nucleotide variants (SNVs) and interferon-λ4 gene (IFNL4) rs368234815 variant in hemodialyzed individuals.MethodsThe study included 83 HD individuals who spontaneously resolved HCV infection (all had known IFNL4 rs368234815 variant) and 104 individuals with persistently positive blood tests for HCV RNA (102 were IFNL4 rs368234815 variant successfully genotyped). We genotyped PON1 by high-resolution melt analysis (rs662) or predesigned TaqMan SNV Genotyping Assay (rs854560, rs705379). We used a logistic regression model to assess the association between genetic data and HCV outcome while adjusting for clinical confounding variables. Epistatic interactions between tested PON1 SNVs and IFNL4 rs368234815 were analyzed by the multifactor dimensionality reduction method.ResultsIn the recessive inheritance model, PON1 rs662 GG (OR 9.94, 95% CI 1.20–82.7, P = 0.022) and rs854560 TT (OR 4.31, 95% CI 1.62–11.5, P = 0.003) genotypes were associated with a higher probability for HCV clearance. The haplotype composed of rs662A_rs854560A_rs705379 was not associated with spontaneous HCV clearance. The IFNL4 rs368234815 TT/TT variant was equally distributed among individuals bearing different PON1 SNVs. The epistatic gene–gene analysis did not reveal the interaction between tested PON1 SNVs and IFNL4 rs368234815 (P = 0.094). Regression model, including the PON1 rs662 GG genotype, the PON1 rs854560 genotype, the IFNL4 rs368234815 TT/TT genotype, age at RRT onset, RRT duration, and chronic glomerulonephritis as possible explanatory variables for spontaneous HCV clearance, showed that significant predictors of spontaneous HCV clearance were the IFNL4 rs368234815 TT/TT genotype (OR 2.607, 95% CI 1.298—5.235, P = 0.007), PON1 rs854560 TT (OR 6.208, 1.962–19.644, P = 0.002), PON1 rs662 GG (OR 10.762, 1.222–94.796, P = 0.032), and RRT duration (OR 0.930, 95% CI 0.879–0.984, P = 0.011).ConclusionIn HD individuals, PON1 rs662 GG and rs854560 TT are associated with a higher frequency of spontaneous HCV clearance.

Highlights

  • To explore associations between PON1 rs854560, rs662, 705,379, Hepatitis C virus (HCV) clearance, and interactions between tested PON1 single nucleotide variants (SNVs) and interferon-λ4 gene (IFNL4) rs368234815 variant in hemodialyzed individuals

  • The IFNL4 rs368234815 TT/TT variant was distributed among individuals bearing different PON1 SNVs (Additional file 1: Tables S2–S4)

  • The epistatic gene–gene analysis did not reveal the interaction between tested PON1 SNVs and IFNL4 rs368234815 (P = 0.094, Table 4)

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Summary

Introduction

To explore associations between PON1 rs854560, rs662 705379, HCV clearance, and interactions between tested PON1 single nucleotide variants (SNVs) and interferon-λ4 gene (IFNL4) rs368234815 variant in hemodialyzed individuals. Outcomes of HCV infection were associated with single nucleotide variants (SNVs) of interferon-λ genes (IFNLs), located on chromosome 19q13 (persistent HCV infection—the TT genotype of IFNL4 rs12979860, the ∆G/∆G genotype of IFNL4 rs368234815 [3], pegylated interferon plus ribavirin treatment-induced clearance— the TT/TT genotype of IFNL4 rs368234815 [4], spontaneous HCV clearance—the CC genotype of IFNL4 rs12979860, the TT/TT genotype of IFNL4 rs368234815 [3, 5, 6], direct-acting antiviral medication-induced HCV clearance—the TT/TT genotype of IFNL4 rs368234815, the TT genotype of IFNL4 rs12979860 [7, 8]). Many other genetic influences were identified or suggested, including PON1 SNVs placed on chromosome 7q21.3 [9,10,11]

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