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HIV infection does not increase the risk of liver complications in hepatitis C virus-infected patient with advanced fibrosis, after sustained virological response with direct-acting antivirals

Authors :
Francisco Téllez
Luis Morano
Ris-Hep
Francisco Jesús Vera-Méndez
María J. Ríos-Villegas
Rosario Palacios Muñoz
Antonio Rivero-Juárez
Gehep study groups
Juan Carlos Alados
Anaïs Corma-Gómez
Juan A. Pineda
Juan Macías
Paloma Geijo
Luis Miguel Real
Source :
Digital.CSIC. Repositorio Institucional del CSIC, instname
Publication Year :
2019
Publisher :
Lippincott Williams & Wilkins, 2019.

Abstract

On behalf of RIS-HEP13 and GEHEP 011 study groups.<br />[Objective]: To assess the impact of HIV coinfection on the risk of developing liver-related complications in HCV-infected patients with advanced fibrosis treated with direct-acting antivirals (DAA) after sustained virological response (SVR).<br />[Design]: Prospective cohort study.<br />[Setting]: Multicenter.<br />[Subjects]: Patients from the GEHEP and HEPAVIR cohorts were selected if they fulfilled the following criteria: treatment against HCV with all oral DAA combination; SVR achievement, defined as undetectable plasma HCV RNA 12 weeks after the end of therapy; pretreatment liver stiffness equal to or higher than 9.5 kPa; liver stiffness measurement at the time of SVR.<br />[Main outcome measure(s)]: The primary variable was the time until the development of a liver complication or requiring liver transplant.<br />[Results]: Seven hundred and seventeen patients were included and 507 (71%) were coinfected with HIV. After a median follow-up time of 21 (14–25) months, 15 (2.1%) patients developed a liver complication and/or underwent a liver transplant and 15 (2.0%) died. The probability of remaining free of hepatic complications or transplant at 1 and 2 was, respectively, 99 and 96% in HCV-monoinfected patients and 99 and 98% in coinfected patients (P = 0.648). In a multivariate analysis, in which nonliver-related death was considered as a competing event, HIV coinfection was not associated with the appearance of hepatic complications or requiring liver transplant [hazard ratio = 0.24; 95% CI (0.03–1.93), P = 0.181]. Having presented hepatic decompensation prior to SVR [hazard ratio = 29.06; 95% CI (3.91–216.16), P < 0.001] and the value of liver stiffness at the SVR time-point (hazard ratio = 1.12; 95% CI (1.07–1.18), P < 0.001] were associated with a higher probability of development of liver events.<br />[Conclusion]: HIV coinfection is not associated with a higher probability of developing liver complications in HCV-infected patients with advanced fibrosis, who achieved SVR with interferon-free regimens.

Details

Language :
English
Database :
OpenAIRE
Journal :
Digital.CSIC. Repositorio Institucional del CSIC, instname
Accession number :
edsair.doi.dedup.....0cb102b4580d2d59a50a49ad2fec3781