Longitudinal evaluation of viral interactions in treated HIV-hepatitis B co-infected patients with additional hepatitis C and D virus

被引:34
作者
Boyd, A. [2 ,3 ]
Lacombe, K. [1 ,2 ,3 ]
Miailhes, P. [4 ]
Gozlan, J. [5 ,6 ]
Bonnard, P. [7 ]
Molina, J. -M. [8 ]
Lascoux-Combe, C. [9 ]
Serfaty, L. [10 ]
Gault, E. [11 ,12 ]
Desvarieux, M. [2 ,3 ,13 ]
Girard, P. -M. [1 ,2 ,3 ]
机构
[1] Hop St Antoine, Serv Malad Infect & Trop, AP HP, F-75012 Paris, France
[2] Univ Paris 06, UMR S707, Paris, France
[3] INSERM, Paris, France
[4] Hosp Civils Lyon, Hotel Dieu, Serv Hepatol & Gastroenterol, Lyon, France
[5] Hop St Antoine, Serv Virol, AP HP, F-75012 Paris, France
[6] Ctr Rech Cordeliers, UMRS 872, Paris, France
[7] Hop Tenon, Serv Malad Infect & Trop, AP HP, F-75970 Paris, France
[8] Hop St Louis, Serv Malad Infect & Trop, AP HP, Paris, France
[9] Hop St Louis, Serv Med Interne, AP HP, Paris, France
[10] Hop St Antoine, Serv Hepatol, AP HP, F-75012 Paris, France
[11] Hop Avicenne, Serv Bacteriol Virol Hyg, AP HP, F-93009 Bobigny, France
[12] Univ Paris 13, EA 3604, Bobigny, France
[13] Columbia Univ, Mailman Sch Publ Hlth, Dept Epidemiol, New York, NY USA
关键词
hepatitis B virus; hepatitis C virus; hepatitis D virus; human immunodeficiency virus; viral replication; ACTIVE ANTIRETROVIRAL THERAPY; ALPHA-2A PLUS RIBAVIRIN; DELTA-VIRUS; COINFECTED PATIENTS; INTERFERON THERAPY; LIVER FIBROSIS; RNA; HBV; QUANTIFICATION; REPLICATION;
D O I
10.1111/j.1365-2893.2009.01153.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Virological interactions of hepatitis B (HBV), hepatitis C (HCV) and hepatitis D (HDV) viruses in HIV-infected patients have been poorly characterized especially under treatment influences. Undetection rates of hepatitis viruses were longitudinally analyzed in a 3-year cohort of 308 HIV-HBV co-infected patients and compared using Generalized Estimating Equation models adjusted for age, HIV-RNA, CD4 cell-count and antiviral treatment. Chronic hepatitis co-infection in HIV-infected patients (age years, SD) was: 265 HBV (40.7, 8.2); 19 HBV-HCV (39.7, 4.1); 12 HBV-HDV (35.2, 9.9); 12 HBV-HCV-HDV (39.2, 5.2). At inclusion, treatment with lamivudine/tenofovir was not significantly different between co-infection groups. HBV suppression was significantly associated with HDV (aOR = 3.85, 95% CI 1.13-13.10, P = 0.03) and HCV tri-infection (aOR = 2.65, 95% CI 1.03-6.81, P = 0.04), but marginally associated with HIV-HBV-HCV-HDV (aOR = 2.32, 95% CI 0.94-5.74, P = 0.07). In quad-infection, lower HDV-undetectability (vs HIV-HBV-HDV, P = 0.2) and higher HCV-undetectability (vs HIV-HBV-HCV, P = 0.1) were demonstrated. The degree of HBV suppression varied between visits and co-infection groups [range of aOR during follow-up (vs HIV-HBV co-infection): HIV-HBV-HCV = 2.23-5.67, HIV-HBV-HDV = 1.53-15.17]. In treated co-infected patients, HDV expressed continuous suppression over HCV- and HBV-replications. Peaks and rebounds from undetectable hepatitis B, C and/or D viremia warrant closer follow-up in this patient population. HDV-replication was uncontrolled even with antiviral treatment.
引用
收藏
页码:65 / 76
页数:12
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