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

被引:17
作者
Corma-Gomez, Anais [1 ]
Morano, Luis [2 ]
Tellez, Francisco [3 ]
Rivero-Juarez, Antonio [4 ]
Real, Luis M. [1 ]
Carlos Alados, Juan [5 ]
Jose Rios-Villegas, Maria [6 ]
Jesus Vera-Mendez, Francisco [7 ]
Palacios Munoz, Rosario [8 ]
Geijo, Paloma [9 ]
Macias, Juan [1 ]
Pineda, Juan A. [1 ]
机构
[1] Hosp Univ Valme, Unit Infect Dis & Microbiol, Seville, Spain
[2] Hosp Univ Alvaro Cunqueiro, Unit Infect Pathol, Vigo, Spain
[3] Univ Cadiz, Hosp Univ Puerto Real, Fac Med, Unit Infect Dis, Cadiz, Spain
[4] Univ Cordoba UCO, Unit Infect Dis, Hosp Univ Reina Sofia, Inst Maimonides Invest Biomed Cordoba IMIBIC, Cordoba, Spain
[5] Univ Hosp Jerez, Unit Clin Microbiol, Cadiz, Spain
[6] Hosp Univ Virgen Macarena, Unit Infect Dis, Seville, Spain
[7] Hosp Gen Univ Santa Lucia, Sect Infect Med, Serv Internal Med, Cartagena, Spain
[8] Hosp Virgen de la Victoria, Unit Infect Dis Microbiol & Prevent Med, Malaga, Spain
[9] Hosp Virgen de la Luz, Unit Infect Dis, Cuenca, Spain
关键词
cirrhosis; direct-acting antivirals; hepatitis C virus; hepatocellular carcinoma; HIV; sustained virological response; INTERFERON PLUS RIBAVIRIN; ALL-CAUSE MORTALITY; COINFECTED PATIENTS; HEPATOCELLULAR-CARCINOMA; PROGRESSION; CIRRHOSIS; STIFFNESS; SURVIVAL; DECOMPENSATION; ERADICATION;
D O I
10.1097/QAD.0000000000002186
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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). Design: Prospective cohort study. Setting: Multicenter. 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. Main outcome measure(s): The primary variable was the time until the development of a liver complication or requiring liver transplant. 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. 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. Copyright (C) 2019 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:1167 / 1174
页数:8
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