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Long-term effect of chronic hepatitis B on mortality in HIV-infected persons in a differential HBV transmission setting

BACKGROUND: There remain gaps in quantifying mortality risk among individuals co-infected with chronic hepatitis B (HBV) and human immunodeficiency virus (HIV) in sub-Saharan African contexts. Among a cohort of HIV-positive individuals in Rwanda, we estimate the difference in time-to mortality betwe...

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Autores principales: Umutesi, Justine, Nsanzimana, Sabin, Yingkai Liu, Carol, Vanella, Patrizio, Ott, Jördis J., Krause, Gérard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9137150/
https://www.ncbi.nlm.nih.gov/pubmed/35624437
http://dx.doi.org/10.1186/s12879-022-07477-1
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author Umutesi, Justine
Nsanzimana, Sabin
Yingkai Liu, Carol
Vanella, Patrizio
Ott, Jördis J.
Krause, Gérard
author_facet Umutesi, Justine
Nsanzimana, Sabin
Yingkai Liu, Carol
Vanella, Patrizio
Ott, Jördis J.
Krause, Gérard
author_sort Umutesi, Justine
collection PubMed
description BACKGROUND: There remain gaps in quantifying mortality risk among individuals co-infected with chronic hepatitis B (HBV) and human immunodeficiency virus (HIV) in sub-Saharan African contexts. Among a cohort of HIV-positive individuals in Rwanda, we estimate the difference in time-to mortality between HBV-positive (HIV/HBV co-infected) and HBV-negative (HIV mono-infected) individuals. METHODS: Using a dataset of HIV-infected adults screened for hepatitis B surface antigen (HBsAg) from January to June 2016 in Rwanda, we performed time-to-event analysis from the date of HBsAg results until death or end of study (31 December 2019). We used the Kaplan–Meier method to estimate probability of survival over time and Cox proportional hazard models to adjust for other factors associated with mortality. RESULTS: Of 21,105 available entries, 18,459 (87.5%) met the inclusion criteria. Mean age was 42.3 years (SD = 11.4) and 394 (2.1%) died during follow-up (mortality rate = 45.7 per 100,000 person-months, 95% confidence interval (CI) 41.4–50.4) Mortality rate ratio for co-infection was 1.7, 95% CI 1.1–2.6, however, Cox regression analysis did not show any association with mortality between compared groups. The adjusted analysis of covariates stratified by co-infection status showed that males, residing outside of the capital Kigali, drinking alcohol, WHO-HIV-clinical stage 3 and 4 were associated with increased mortality in this HIV cohort. CONCLUSIONS: HBV infection does not significantly influence mortality among HIV-infected individuals in Rwanda. The current cohort is likely to have survived a period of high-risk exposure to HBV and HIV mortality and limited health care until their diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-022-07477-1.
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spelling pubmed-91371502022-05-28 Long-term effect of chronic hepatitis B on mortality in HIV-infected persons in a differential HBV transmission setting Umutesi, Justine Nsanzimana, Sabin Yingkai Liu, Carol Vanella, Patrizio Ott, Jördis J. Krause, Gérard BMC Infect Dis Research BACKGROUND: There remain gaps in quantifying mortality risk among individuals co-infected with chronic hepatitis B (HBV) and human immunodeficiency virus (HIV) in sub-Saharan African contexts. Among a cohort of HIV-positive individuals in Rwanda, we estimate the difference in time-to mortality between HBV-positive (HIV/HBV co-infected) and HBV-negative (HIV mono-infected) individuals. METHODS: Using a dataset of HIV-infected adults screened for hepatitis B surface antigen (HBsAg) from January to June 2016 in Rwanda, we performed time-to-event analysis from the date of HBsAg results until death or end of study (31 December 2019). We used the Kaplan–Meier method to estimate probability of survival over time and Cox proportional hazard models to adjust for other factors associated with mortality. RESULTS: Of 21,105 available entries, 18,459 (87.5%) met the inclusion criteria. Mean age was 42.3 years (SD = 11.4) and 394 (2.1%) died during follow-up (mortality rate = 45.7 per 100,000 person-months, 95% confidence interval (CI) 41.4–50.4) Mortality rate ratio for co-infection was 1.7, 95% CI 1.1–2.6, however, Cox regression analysis did not show any association with mortality between compared groups. The adjusted analysis of covariates stratified by co-infection status showed that males, residing outside of the capital Kigali, drinking alcohol, WHO-HIV-clinical stage 3 and 4 were associated with increased mortality in this HIV cohort. CONCLUSIONS: HBV infection does not significantly influence mortality among HIV-infected individuals in Rwanda. The current cohort is likely to have survived a period of high-risk exposure to HBV and HIV mortality and limited health care until their diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-022-07477-1. BioMed Central 2022-05-27 /pmc/articles/PMC9137150/ /pubmed/35624437 http://dx.doi.org/10.1186/s12879-022-07477-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Umutesi, Justine
Nsanzimana, Sabin
Yingkai Liu, Carol
Vanella, Patrizio
Ott, Jördis J.
Krause, Gérard
Long-term effect of chronic hepatitis B on mortality in HIV-infected persons in a differential HBV transmission setting
title Long-term effect of chronic hepatitis B on mortality in HIV-infected persons in a differential HBV transmission setting
title_full Long-term effect of chronic hepatitis B on mortality in HIV-infected persons in a differential HBV transmission setting
title_fullStr Long-term effect of chronic hepatitis B on mortality in HIV-infected persons in a differential HBV transmission setting
title_full_unstemmed Long-term effect of chronic hepatitis B on mortality in HIV-infected persons in a differential HBV transmission setting
title_short Long-term effect of chronic hepatitis B on mortality in HIV-infected persons in a differential HBV transmission setting
title_sort long-term effect of chronic hepatitis b on mortality in hiv-infected persons in a differential hbv transmission setting
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9137150/
https://www.ncbi.nlm.nih.gov/pubmed/35624437
http://dx.doi.org/10.1186/s12879-022-07477-1
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