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Renal function in Ethiopian HIV-positive adults on antiretroviral treatment with and without tenofovir
BACKGROUND: Limited data are available on the effect of antiretroviral treatment (ART) or Tenofovir disoproxil fumarate (TDF) on renal function in Ethiopians. We aimed to assess factors associated with renal function changes during the first year of ART with special focus on TDF. METHODS: HIV positi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409649/ https://www.ncbi.nlm.nih.gov/pubmed/32762646 http://dx.doi.org/10.1186/s12879-020-05308-9 |
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author | Yilma, Daniel Abdissa, Alemseged Kæstel, Pernille Tesfaye, Markos Olsen, Mette F. Girma, Tsinuel Ritz, Christian Friis, Henrik Andersen, Åse B. Kirk, Ole |
author_facet | Yilma, Daniel Abdissa, Alemseged Kæstel, Pernille Tesfaye, Markos Olsen, Mette F. Girma, Tsinuel Ritz, Christian Friis, Henrik Andersen, Åse B. Kirk, Ole |
author_sort | Yilma, Daniel |
collection | PubMed |
description | BACKGROUND: Limited data are available on the effect of antiretroviral treatment (ART) or Tenofovir disoproxil fumarate (TDF) on renal function in Ethiopians. We aimed to assess factors associated with renal function changes during the first year of ART with special focus on TDF. METHODS: HIV positive persons who were ≥ 18 years of age and eligible for ART initiation were recruited. Creatinine measurement to estimate glomerular filtration rate (eGFR) and spot urine analyses were performed at baseline and after 3, 6 and 12 months of ART. Univariate and multivariate linear regression and univariate logistic regression were used to determine factors associated with eGFR as continuous and categorical variable respectively. A linear mixed model was used to assess 12 month eGFR difference in TDF and non-TDF based regimen. RESULT: Of 340 ART-naïve HIV patients with baseline renal function tests, 82.3% (279/339) were initiated on a TDF based ART regimen. All patients were on non-nucleoside reverse transcriptase inhibitors (NNRTI) based ART regimen. The median (IQR) change in eGFR with 12 months of ART was 0.8 (− 11.1; 10.0) ml/min/1.73m(2). About 41 and 26.9% of HIV patients had a drop of greater than 3 and 10 mL/min/1.73 m(2) in eGFR at 12 month, respectively. However, none of the HIV patients declined to < 60 ml/min/1.73m(2) within 12 months. Moreover, none of the HIV patients had persistent proteinuria or glycosuria. Older HIV patients especially age > 45 years and those with unsuppressed viral load at 6 month of ART had a significantly lower eGFR at 12 months of ART initiation. However, there was no difference in 12 month eGFR between HIV patients initiated on TDF based regimen and non-TDF based regimen. CONCLUSION: Renal function remained stable with no difference between HIV patients treated with TDF or non-TDF NNRTI based ART regimen over 12 months. However, older HIV patients and those with unsuppressed viral load deserve special focus on renal monitoring. Data on long-term safety of TDF (> 1 year) is still warranted in this population. |
format | Online Article Text |
id | pubmed-7409649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74096492020-08-10 Renal function in Ethiopian HIV-positive adults on antiretroviral treatment with and without tenofovir Yilma, Daniel Abdissa, Alemseged Kæstel, Pernille Tesfaye, Markos Olsen, Mette F. Girma, Tsinuel Ritz, Christian Friis, Henrik Andersen, Åse B. Kirk, Ole BMC Infect Dis Research Article BACKGROUND: Limited data are available on the effect of antiretroviral treatment (ART) or Tenofovir disoproxil fumarate (TDF) on renal function in Ethiopians. We aimed to assess factors associated with renal function changes during the first year of ART with special focus on TDF. METHODS: HIV positive persons who were ≥ 18 years of age and eligible for ART initiation were recruited. Creatinine measurement to estimate glomerular filtration rate (eGFR) and spot urine analyses were performed at baseline and after 3, 6 and 12 months of ART. Univariate and multivariate linear regression and univariate logistic regression were used to determine factors associated with eGFR as continuous and categorical variable respectively. A linear mixed model was used to assess 12 month eGFR difference in TDF and non-TDF based regimen. RESULT: Of 340 ART-naïve HIV patients with baseline renal function tests, 82.3% (279/339) were initiated on a TDF based ART regimen. All patients were on non-nucleoside reverse transcriptase inhibitors (NNRTI) based ART regimen. The median (IQR) change in eGFR with 12 months of ART was 0.8 (− 11.1; 10.0) ml/min/1.73m(2). About 41 and 26.9% of HIV patients had a drop of greater than 3 and 10 mL/min/1.73 m(2) in eGFR at 12 month, respectively. However, none of the HIV patients declined to < 60 ml/min/1.73m(2) within 12 months. Moreover, none of the HIV patients had persistent proteinuria or glycosuria. Older HIV patients especially age > 45 years and those with unsuppressed viral load at 6 month of ART had a significantly lower eGFR at 12 months of ART initiation. However, there was no difference in 12 month eGFR between HIV patients initiated on TDF based regimen and non-TDF based regimen. CONCLUSION: Renal function remained stable with no difference between HIV patients treated with TDF or non-TDF NNRTI based ART regimen over 12 months. However, older HIV patients and those with unsuppressed viral load deserve special focus on renal monitoring. Data on long-term safety of TDF (> 1 year) is still warranted in this population. BioMed Central 2020-08-06 /pmc/articles/PMC7409649/ /pubmed/32762646 http://dx.doi.org/10.1186/s12879-020-05308-9 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article Yilma, Daniel Abdissa, Alemseged Kæstel, Pernille Tesfaye, Markos Olsen, Mette F. Girma, Tsinuel Ritz, Christian Friis, Henrik Andersen, Åse B. Kirk, Ole Renal function in Ethiopian HIV-positive adults on antiretroviral treatment with and without tenofovir |
title | Renal function in Ethiopian HIV-positive adults on antiretroviral treatment with and without tenofovir |
title_full | Renal function in Ethiopian HIV-positive adults on antiretroviral treatment with and without tenofovir |
title_fullStr | Renal function in Ethiopian HIV-positive adults on antiretroviral treatment with and without tenofovir |
title_full_unstemmed | Renal function in Ethiopian HIV-positive adults on antiretroviral treatment with and without tenofovir |
title_short | Renal function in Ethiopian HIV-positive adults on antiretroviral treatment with and without tenofovir |
title_sort | renal function in ethiopian hiv-positive adults on antiretroviral treatment with and without tenofovir |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409649/ https://www.ncbi.nlm.nih.gov/pubmed/32762646 http://dx.doi.org/10.1186/s12879-020-05308-9 |
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