Back to Search
Start Over
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
- 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.
- Subjects :
- 0301 basic medicine
Liver Cirrhosis
Male
Cirrhosis
Sustained Virologic Response
Hepatocellular carcinoma
medicine.medical_treatment
HIV Infections
Hepacivirus
Liver transplantation
medicine.disease_cause
Direct-acting antivirals
0302 clinical medicine
Immunology and Allergy
030212 general & internal medicine
Prospective Studies
Prospective cohort study
Coinfection
Hepatitis C virus
virus diseases
Middle Aged
Viral Load
Hepatitis C
Sustained virological response
Infectious Diseases
Drug Therapy, Combination
Female
Viral load
medicine.medical_specialty
Immunology
Antiviral Agents
03 medical and health sciences
Pharmacotherapy
Internal medicine
medicine
Humans
Proportional Hazards Models
business.industry
Proportional hazards model
HIV
medicine.disease
digestive system diseases
Transplant Recipients
Liver Transplantation
030104 developmental biology
business
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Digital.CSIC. Repositorio Institucional del CSIC, instname
- Accession number :
- edsair.doi.dedup.....0cb102b4580d2d59a50a49ad2fec3781