Background and objective: Hepatitis C virus (HCV) infection is frequent in HIV-positive subjects. We evaluated the potential impact of HCV coinfection and other determinants on HIV disease progression in a cohort of long-term non-progressors (LTNPs). Study design: We studied immunological and virological factors in a cohort of 49 LTNPs, 23 of whom progressed during the follow-up (late progressors; LPs). Results: HCV coinfection was detected in 19/26 LTNPs and 15/23 LPs. Univariate analysis showed that HIV viral load was associated with disease progression (P = 0.04), and time-to-event analysis indicated that HCV genotype 1 significantly correlated with LTNP status (P = 0.031). At multivariate analysis, HIV viremia at study entry remained independently associated with LTNP status (P = 0.049). When the most represented genotypes (1 and 3a) were considered in the model, genotype 3a infection (P = 0.034) and gender (P = 0.035) emerged as independent variables related to HIV disease progression, whereas HIV viral load disappeared. Conclusions: In addition to HIV viremia, coinfection with different HCV genotypes and gender may affect LTNP status. (C) 2007 Elsevier B.V. All rights reserved.

Hepatitis C virus (HCV) coinfection in a cohort of HIV positive long-term non-progressors: Possible protective effect of infecting HCV genotype on HIV disease progression

POLI , GUIDO
2007-01-01

Abstract

Background and objective: Hepatitis C virus (HCV) infection is frequent in HIV-positive subjects. We evaluated the potential impact of HCV coinfection and other determinants on HIV disease progression in a cohort of long-term non-progressors (LTNPs). Study design: We studied immunological and virological factors in a cohort of 49 LTNPs, 23 of whom progressed during the follow-up (late progressors; LPs). Results: HCV coinfection was detected in 19/26 LTNPs and 15/23 LPs. Univariate analysis showed that HIV viral load was associated with disease progression (P = 0.04), and time-to-event analysis indicated that HCV genotype 1 significantly correlated with LTNP status (P = 0.031). At multivariate analysis, HIV viremia at study entry remained independently associated with LTNP status (P = 0.049). When the most represented genotypes (1 and 3a) were considered in the model, genotype 3a infection (P = 0.034) and gender (P = 0.035) emerged as independent variables related to HIV disease progression, whereas HIV viral load disappeared. Conclusions: In addition to HIV viremia, coinfection with different HCV genotypes and gender may affect LTNP status. (C) 2007 Elsevier B.V. All rights reserved.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/11717
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