TY - JOUR
T1 - Hepatitis C virus (HCV) coinfection in a cohort of HIV positive long-term non-progressors
T2 - Possible protective effect of infecting HCV genotype on HIV disease progression
AU - Morsica, Giulia
AU - Bagaglio, Sabrina
AU - Ghezzi, Silvia
AU - Lodrini, Chiara
AU - Vicenzi, Elisa
AU - Santagostino, Elena
AU - Gringeri, Alessandro
AU - Cusini, Marco
AU - Carminati, Guido
AU - Bianchi, Giampaolo
AU - Galli, Laura
AU - Lazzarin, Adriano
AU - Poli, Guido
PY - 2007/6
Y1 - 2007/6
N2 - 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.
AB - 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.
KW - HCV genotype
KW - HIV disease progression
KW - HIV load
KW - LTNPs
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U2 - 10.1016/j.jcv.2007.03.007
DO - 10.1016/j.jcv.2007.03.007
M3 - Article
C2 - 17434339
AN - SCOPUS:34249084372
SN - 1386-6532
VL - 39
SP - 82
EP - 86
JO - Journal of Clinical Virology
JF - Journal of Clinical Virology
IS - 2
ER -