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

  1. 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
    Kopp, Jeffrey B
    Kimmel, Paul L
    Wester, C William [ORCID]
  2. Author Address

    Vanderbilt Institute for Global Health (VIGH), Nashville, TN, USA., Department of Health Policy, Vanderbilt University Medical Center, Nashville, TN, USA., Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA., Department of Medicine, Aminu Kano Teaching Hospital, Kano, Nigeria., Department of Pathology, Bayero University, Aminu Kano Teaching Hospital, Kano, Nigeria., Department of Medicine, Division of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, USA., Department of Medicine, Division of Nephrology, Vanderbilt University Medical Center, Nashville, TN, USA., Basic Research Laboratory, Molecular Genetic Epidemiology Section, Frederick National Laboratory for Cancer Research sponsored by the National Cancer Institute, NIH, Frederick, MD, USA., National Institute of Diabetes and Digestive and Kidney Diseases, Division of Kidney, Urologic and Hematologic Diseases, NIH, Bethesda, MD, USA., Vanderbilt Institute for Global Health (VIGH), Nashville, TN, USA. william.wester@vumc.org., Department of Medicine, Division of Infectious Diseases, Vanderbilt University Medical Center, Nashville, TN, USA. william.wester@vumc.org.,
    1. Year: 2019
    2. Date: Jun 10
    3. Epub Date: 2019 06 10
  1. Journal: Trials
    1. 20
    2. 1
    3. Pages: 341
  2. Type of Article: Article
  3. Article Number: 341
  4. ISSN: 1745-6215
  1. Abstract:

    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.

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External Sources

  1. DOI: 10.1186/s13063-019-3436-y
  2. PMID: 31182139
  3. WOS: 000471348400009
  4. PII : 10.1186/s13063-019-3436-y

Library Notes

  1. Fiscal Year: FY2018-2019
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