Hepatitis B virus coinfection is associated with high early mortality in HIV-infected Tanzanians on antiretroviral therapy.


Journal

AIDS (London, England)
ISSN: 1473-5571
Titre abrégé: AIDS
Pays: England
ID NLM: 8710219

Informations de publication

Date de publication:
01 03 2019
Historique:
entrez: 1 2 2019
pubmed: 1 2 2019
medline: 4 3 2020
Statut: ppublish

Résumé

There is limited data on the effect of antiviral therapies on clinical outcomes in HIV and hepatitis B virus (HBV)-infected individuals in sub-Saharan Africa. Single center, prospective longitudinal cohort study at Management and Development for Health supported HIV Care and Treatment clinics in Dar es Salaam, Tanzania. Between April 2014 and December 2015, HIV-infected, HBV-infected and HIV/HBV-coinfected, treatment naïve, Tanzanian adults more than 18 years of age were eligible for enrollment and followed for 10-18 months after initiating antivirals. All HIV-infected and HIV/HBV-coinfected participants received tenofovir, lamivudine and efavirenz; HBV-infected participants received lamivudine. Multivariate regression models were constructed to identify factors associated with mortality in HIV-infected and HIV/HBV-coinfected participants. A total of 265 HIV-infected, 165 HBV-infected and 64 HIV/HBV-coinfected participants were analyzed. At baseline, HBV-infected participants were younger and had a higher BMI than HIV-infected and HIV/HBV-coinfected participants. After a median of 371 (interquartile range 50) days on treatment, there were 40 deaths. Mortality was significantly higher among HIV/HBV-coinfected participants compared with HIV and HBV-infected participants [HIV/HBV-coinfected 12 of 64 (19%) vs. HIV-infected 26 of 265 (10%) and HBV-infected two of 265 (1%), P < 0.01]. High baseline HIV RNA and low hemoglobin levels, but not HBV coinfection were independently associated with early mortality in multivariate analyses of HIV-infected participants. High rates of early mortality were observed after treatment initiation in HIV/HBV-coinfected individuals compared with participants with HIV or HBV alone, despite robust aspartate aminotransferase to platelet ratio index declines and high rates of virologic suppression. HIV rather than HBV-related factors are more important contributors to mortality in these individuals.

Identifiants

pubmed: 30702515
doi: 10.1097/QAD.0000000000002073
pii: 00002030-201903010-00014
doi:

Substances chimiques

Anti-Retroviral Agents 0

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

465-473

Subventions

Organisme : NIDDK NIH HHS
ID : K23 DK095707
Pays : United States

Commentaires et corrections

Type : CommentIn

Auteurs

Beatrice Christian (B)

Management and Development for Health, Dar es Salaam, Tanzania.

Emanuel Fabian (E)

Management and Development for Health, Dar es Salaam, Tanzania.

Irene Macha (I)

Management and Development for Health, Dar es Salaam, Tanzania.

Shida Mpangala (S)

Management and Development for Health, Dar es Salaam, Tanzania.

Chloe L Thio (CL)

Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.

Nzovu Ulenga (N)

Management and Development for Health, Dar es Salaam, Tanzania.

Ferdinand Mugusi (F)

Department of Medicine, Muhumbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.

Lauren R Ammerman (LR)

Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Wafaie Fawzi (W)

Departments of Nutrition, Epidemiology and Global Health and Population, Harvard T. H Chan School of Public Health, Boston, Massachusetts.

Richard Green (R)

Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.

Robert Murphy (R)

Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.

Claudia Hawkins (C)

Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.

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Classifications MeSH