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Does HIV-infection influence the response of chronic hepatitis C to interferon treatment? A French multicenter prospective study

Authors :
H. Desmorat
F Bloch
Jacques Izopet
Daniel Fischer
B Mesnard
Pierre-Henri Bernard
François Bailly
J.-P. Lagasse
P. Couzigou
C Sayada
P Chossegros
G Force
Xavier Causse
Jean-Louis Payen
Marie-France Saint-Marc Girardin
J.C. Barbare
D Trois Vallets
Jean-Dominique Poveda
JC Schmit
Alexandre Pariente
P Sogni
Jean-Pierre Zarski
Albert Tran
Gérard Babany
L. Bettan
A Gauthier
Y Bacq
Eveline Boucher
Puig P Laurent
JM Lang
C Douvin
R Olivares
C Housset
Nathalie Boyer
W Rozenbaum
J.-J. Raabe
C Van Lemmens
O Danne
F. Montestruc
Source :
Journal of Hepatology. 32:1003-1010
Publication Year :
2000
Publisher :
Elsevier BV, 2000.

Abstract

Background/Aim: The aim of this prospective study was to compare the response to alfa-interferon treatment of chronic hepatitis C in two groups of patients: coinfected with human immunodeficiency virus (HIV) (G I) or not (G II). Methods: One hundred and fifty-three patients with chronic hepatitis C had been enrolled in 30 French liver units or infectious diseases units between May 1992 and January 1995 (G I: 76, G II: 77) to receive alfa-2a interferon: 3 MU thrice weekly for 6 months. Results: One hundred and twenty-seven patients (G I: 63, G II: 64) fulfilled all criteria for analysis. The two groups were comparable for all demographic data, while significantly more severe biological and histological ( p =0.001) parameters attested to more serious hepatitis among HIV-HCV coinfected patients. HCV viremia was higher among HIV-coinfected patients ( p =0.0169), while genotype repartition was identical among the two groups (more than 52% of genotype 1, more than 31% of genotype 3). ALT normalization was, respectively, (G I/G II) obtained in 17.46%/26.56% (not significant) of patients at the end of treatment and in 11.11%/12.5% (not significant) of patients after 6 months of follow-up. In a multivariate analysis, GGT level before therapy (relative risk 2.1, confidence interval 1.1–5.8) and body surface area (relative risk 1.9, confidence interval 1.1–3.7) were the variables independently associated with the response to alfa-interferon treatment (higher GGT and more elevated body surface area were associated with a risk of non-response). Conclusion: In our study HIV infection did not affect the alfa-interferon treatment response of chronic hepatitis C, and response could be achieved among HIV-coinfected patients. Present therapeutic anti-HCV schedules need to be proposed to HIV-HCV coinfected patients before severe immunosuppression occurs. On the other hand, more severe biological and histological parameters were observed among HIV-HCV coinfected patients, which suggests a need to study whether HIV infection is associated with a worsening course of chronic hepatitis C.

Details

ISSN :
01688278
Volume :
32
Database :
OpenAIRE
Journal :
Journal of Hepatology
Accession number :
edsair.doi...........1c6d7e0c404a457c037ec40b54ab7352
Full Text :
https://doi.org/10.1016/s0168-8278(00)80105-1