Long-term Hepatitis B and Liver Outcomes Among Adults Taking Tenofovir-Containing Antiretroviral Therapy for HBV/HIV Coinfection in Zambia

被引:3
作者
Vinikoor, Michael J. [1 ,2 ,3 ,12 ]
Hamusonde, Kalongo [1 ,4 ,5 ]
Muula, Guy [1 ]
Asombang, Mah [1 ]
Riebensahm, Carlotta [4 ,5 ]
Chitundu, Helen [6 ]
Sunkuntu-Sichizya, Veronica [6 ]
Bhattacharya, Debika [7 ]
Sinkala, Edford [3 ,8 ]
Lauer, Georg [9 ]
Chung, Raymond [9 ]
Mbewe, Wilson [10 ]
Egger, Matthias [4 ]
Bosomprah, Samuel [1 ,11 ]
Wandeler, Gilles [4 ,5 ]
机构
[1] Ctr Infect Dis Res Zambia, Res Dept, Lusaka, Zambia
[2] Univ Alabama Birmingham, Dept Med, Birmingham, AL USA
[3] Univ Zambia, Sch Med, Lusaka, Zambia
[4] Univ Bern, Inst Social & Prevent Med, Bern, Switzerland
[5] Bern Univ Hosp, Univ Bern, Dept Infect Dis, Bern, Switzerland
[6] Univ Teaching Hosp, Dept Radiol, Lusaka, Zambia
[7] Univ Calif Los Angeles, Dept Med, Los Angeles, CA USA
[8] Univ Teaching Hosp, Dept Med, Lusaka, Zambia
[9] Massachusetts Gen Hosp, Liver Ctr, Dept Med, Boston, MA USA
[10] Kanyama Level 1 Hosp, Kanyama Level Hosp 1, Lusaka, Zambia
[11] Univ Ghana, Sch Publ Hlth, Dept Biostat, Accra, Ghana
[12] Ctr Infect Dis Res Zambia, Plot 34620,Corner Lukasu & Danny Pule Rd, Lusaka, Zambia
基金
美国国家卫生研究院; 瑞士国家科学基金会;
关键词
hepatitis B; HIV/AIDS; liver fibrosis; hepatocellular carcinoma; antiviral therapy; HUMAN-IMMUNODEFICIENCY-VIRUS; TRANSIENT ELASTOGRAPHY; INFECTED ADULTS; HBV COINFECTION; HIV; MORTALITY; STIFFNESS; FIBROSIS; COHORT; IMPACT;
D O I
10.1093/cid/ciad654
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Long-term outcomes of tenofovir-containing antiretroviral therapy (ART) for hepatitis B virus (HBV)/human immunodeficiency virus (HIV) coinfection were evaluated in Zambia.Methods A prospective cohort of adults with HIV and hepatitis B surface antigen (HBsAg)-positivity was enrolled at ART initiation. On tenofovir-containing ART, we ascertained HBV viral load (VL) non-suppression, alanine aminotransferase (ALT) elevation, serologic end-points, progression of liver fibrosis based on elastography, and hepatocellular carcinoma (HCC) incidence. We also described a subgroup (low HBV VL and no/minimal fibrosis at baseline) that, under current international guidelines, would not have been treated in the absence of their HIV infection.Results Among 289 participants at ART start, median age was 34 years, 40.1% were women, median CD4 count was 191 cells/mm3, 44.2% were hepatitis B e antigen-positive, and 28.4% had liver fibrosis/cirrhosis. Over median 5.91 years of ART, 13.6% developed HBV viral non-suppression, which was associated with advanced HIV disease. ALT elevation on ART was linked with HBV VL non-suppression. Regression of fibrosis and cirrhosis were common, progression to cirrhosis was absent, and no cases of HCC were ascertained. HBsAg seroclearance was 9.4% at 2 and 15.4% at 5 years, with higher rates among patients with low baseline HBV replication markers.Conclusions Reassuring long-term liver outcomes were ascertained during tenofovir-based ART for HBV/HIV coinfection in Zambia. Higher than expected HBsAg seroclearance during ART underscores the need to include people with HIV in HBV cure research. 6-year hepatitis B viral and liver outcomes of ART-treated HBVHIV coinfection were reassuring in Zambia. HBV DNA non-suppression and alanine aminotransferase ALT elevation persisted in some patients. High hepatitis B surface antigen clearance rates should motivate additional research in this population.
引用
收藏
页码:1583 / 1590
页数:8
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