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Optimal management of HIV- positive adults at risk for kidney disease in Nigeria (Renal Risk Reduction “R3” Trial): protocol and study design

BACKGROUND: Individuals with two copies of the apolipoprotein-1 (APOL1) gene risk variants are at high risk (HR) for non-diabetic kidney disease. The presence of these risk variants is highest in West Africa, specifically in Nigeria. However, there is limited availability of dialysis and kidney tran...

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Autores principales: Aliyu, Muktar H., Wudil, Usman J., Ingles, Donna J., Shepherd, Bryan E., Gong, Wu, Musa, Baba M., Muhammad, Hamza, Sani, Mahmoud U., Abdu, Aliyu, Nalado, Aisha M., Atanda, Akinfenwa, Ahonkhai, Aima A., Ikizler, Talat A., Winkler, Cheryl A., Kopp, Jeffrey B., Kimmel, Paul L., Wester, C. William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558910/
https://www.ncbi.nlm.nih.gov/pubmed/31182139
http://dx.doi.org/10.1186/s13063-019-3436-y
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author Aliyu, Muktar H.
Wudil, Usman J.
Ingles, Donna J.
Shepherd, Bryan E.
Gong, Wu
Musa, Baba M.
Muhammad, Hamza
Sani, Mahmoud U.
Abdu, Aliyu
Nalado, Aisha M.
Atanda, Akinfenwa
Ahonkhai, Aima A.
Ikizler, Talat A.
Winkler, Cheryl A.
Kopp, Jeffrey B.
Kimmel, Paul L.
Wester, C. William
author_facet Aliyu, Muktar H.
Wudil, Usman J.
Ingles, Donna J.
Shepherd, Bryan E.
Gong, Wu
Musa, Baba M.
Muhammad, Hamza
Sani, Mahmoud U.
Abdu, Aliyu
Nalado, Aisha M.
Atanda, Akinfenwa
Ahonkhai, Aima A.
Ikizler, Talat A.
Winkler, Cheryl A.
Kopp, Jeffrey B.
Kimmel, Paul L.
Wester, C. William
author_sort Aliyu, Muktar H.
collection PubMed
description BACKGROUND: Individuals with two copies of the apolipoprotein-1 (APOL1) gene risk variants are at high risk (HR) for non-diabetic kidney disease. The presence of these risk variants is highest in West Africa, specifically in Nigeria. However, there is limited availability of dialysis and kidney transplantation in Nigeria, and most individuals will die soon after developing end-stage renal disease. Blocking the renin angiotensin aldosterone system with angiotensin-converting enzyme inhibitors (ACEi) is a well-recognized strategy to slow renal disease progression in patients with diabetes mellitus with chronic kidney disease (CKD) and in patients with HIV-associated nephropathy. We propose to determine whether presence of the APOL1 HR genotype alters or predicts responsiveness to conventional therapy to treat or prevent CKD and if addition of an ACEi to standard combination antiretroviral therapy (ART) reduces the risk of kidney complications among non-diabetic Nigerian adults. METHODS/DESIGN: We will screen 2600 HIV-positive adults who have received ART to (1) determine the prevalence of APOL1 risk variants and assess whether APOL1 HR status correlates with prevalent albuminuria, estimated glomerular filtration rate (eGFR), and/or prevalent CKD; (2) assess, via a randomized, placebo-controlled trial (RCT) in a subset of these participants with microalbuminura (n = 280) whether addition of the ACEi, lisinopril, compared to standard of care, significantly reduces the incidence or progression of albuminuria; and (3) determine whether the APOL1 HR genotype is associated with worse kidney outcomes (i.e. eGFR slope or regression of albuminuria) among participants in the RCT. CONCLUSIONS: This study will examine the increasing prevalence of kidney diseases in HIV-positive adults in a West African population, and the relationship between these diseases and the APOL1 high-risk genotype. By evaluating the addition of an ACEi to the care of individuals with HIV infection who have albuminuria, our trial will provide definitive evidence to guide strategies for management and clinical care in this population, with the goal of reducing HIV-related kidney complications. TRIAL REGISTRATION: ClinicalTrials.gov, NCT03201939. Registered on 26 August 2016. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-019-3436-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-65589102019-06-13 Optimal management of HIV- positive adults at risk for kidney disease in Nigeria (Renal Risk Reduction “R3” Trial): protocol and study design Aliyu, Muktar H. Wudil, Usman J. Ingles, Donna J. Shepherd, Bryan E. Gong, Wu Musa, Baba M. Muhammad, Hamza Sani, Mahmoud U. Abdu, Aliyu Nalado, Aisha M. Atanda, Akinfenwa Ahonkhai, Aima A. Ikizler, Talat A. Winkler, Cheryl A. Kopp, Jeffrey B. Kimmel, Paul L. Wester, C. William Trials Study Protocol BACKGROUND: Individuals with two copies of the apolipoprotein-1 (APOL1) gene risk variants are at high risk (HR) for non-diabetic kidney disease. The presence of these risk variants is highest in West Africa, specifically in Nigeria. However, there is limited availability of dialysis and kidney transplantation in Nigeria, and most individuals will die soon after developing end-stage renal disease. Blocking the renin angiotensin aldosterone system with angiotensin-converting enzyme inhibitors (ACEi) is a well-recognized strategy to slow renal disease progression in patients with diabetes mellitus with chronic kidney disease (CKD) and in patients with HIV-associated nephropathy. We propose to determine whether presence of the APOL1 HR genotype alters or predicts responsiveness to conventional therapy to treat or prevent CKD and if addition of an ACEi to standard combination antiretroviral therapy (ART) reduces the risk of kidney complications among non-diabetic Nigerian adults. METHODS/DESIGN: We will screen 2600 HIV-positive adults who have received ART to (1) determine the prevalence of APOL1 risk variants and assess whether APOL1 HR status correlates with prevalent albuminuria, estimated glomerular filtration rate (eGFR), and/or prevalent CKD; (2) assess, via a randomized, placebo-controlled trial (RCT) in a subset of these participants with microalbuminura (n = 280) whether addition of the ACEi, lisinopril, compared to standard of care, significantly reduces the incidence or progression of albuminuria; and (3) determine whether the APOL1 HR genotype is associated with worse kidney outcomes (i.e. eGFR slope or regression of albuminuria) among participants in the RCT. CONCLUSIONS: This study will examine the increasing prevalence of kidney diseases in HIV-positive adults in a West African population, and the relationship between these diseases and the APOL1 high-risk genotype. By evaluating the addition of an ACEi to the care of individuals with HIV infection who have albuminuria, our trial will provide definitive evidence to guide strategies for management and clinical care in this population, with the goal of reducing HIV-related kidney complications. TRIAL REGISTRATION: ClinicalTrials.gov, NCT03201939. Registered on 26 August 2016. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-019-3436-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-10 /pmc/articles/PMC6558910/ /pubmed/31182139 http://dx.doi.org/10.1186/s13063-019-3436-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Study Protocol
Aliyu, Muktar H.
Wudil, Usman J.
Ingles, Donna J.
Shepherd, Bryan E.
Gong, Wu
Musa, Baba M.
Muhammad, Hamza
Sani, Mahmoud U.
Abdu, Aliyu
Nalado, Aisha M.
Atanda, Akinfenwa
Ahonkhai, Aima A.
Ikizler, Talat A.
Winkler, Cheryl A.
Kopp, Jeffrey B.
Kimmel, Paul L.
Wester, C. William
Optimal management of HIV- positive adults at risk for kidney disease in Nigeria (Renal Risk Reduction “R3” Trial): protocol and study design
title Optimal management of HIV- positive adults at risk for kidney disease in Nigeria (Renal Risk Reduction “R3” Trial): protocol and study design
title_full Optimal management of HIV- positive adults at risk for kidney disease in Nigeria (Renal Risk Reduction “R3” Trial): protocol and study design
title_fullStr Optimal management of HIV- positive adults at risk for kidney disease in Nigeria (Renal Risk Reduction “R3” Trial): protocol and study design
title_full_unstemmed Optimal management of HIV- positive adults at risk for kidney disease in Nigeria (Renal Risk Reduction “R3” Trial): protocol and study design
title_short Optimal management of HIV- positive adults at risk for kidney disease in Nigeria (Renal Risk Reduction “R3” Trial): protocol and study design
title_sort optimal management of hiv- positive adults at risk for kidney disease in nigeria (renal risk reduction “r3” trial): protocol and study design
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558910/
https://www.ncbi.nlm.nih.gov/pubmed/31182139
http://dx.doi.org/10.1186/s13063-019-3436-y
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