Prognostic model for nephrotoxicity among HIV-positive Zambian adults receiving tenofovir disoproxil fumarate-based antiretroviral therapy.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 23 03 2021
accepted: 22 05 2021
entrez: 12 7 2021
pubmed: 13 7 2021
medline: 29 10 2021
Statut: epublish

Résumé

Persons living with HIV (PLWH) receiving tenofovir disoproxil fumarate (TDF)-based antiretroviral therapy (ART) risk suffering TDF-associated nephrotoxicity (TDFAN). TDFAN can result in short- and long-term morbidity, including permanent loss of kidney function, chronic kidney disease (CKD), and end-stage kidney disease (ESKD) requiring dialysis. Currently, there is no model to predict this risk or discern which patients to initiate TDF-based therapy. Consequently, some patients suffer TDFAN within the first few months of initiating therapy before switching to another suitable antiretroviral or a lower dose of TDF. In a prospective observational cohort study of adult Zambian PLWH, we modelled the risk for TDFAN before initiating therapy to identify individuals at high risk for experiencing AKI after initiating TDF-based therapy. We enrolled 205 HIV-positive, ART-naïve adults initiating TDF-based therapy followed for a median of 3.4 months for TDFAN at the Adult Infectious Disease Research Centre (AIDC) in Lusaka, Zambia. We defined TDFAN as meeting any of these acute kidney disease (AKD) criteria: 1) An episode of estimated glomerular filtration rate (eGFR)< 60ml/ min/1.73m2 within 3 months, 2) reduced eGFR by> 35% within 3 months or 3) increased serum creatinine by> 50% within 3 months. A total of 45 participants (22%) developed acute kidney disease (AKD) after TDF-based therapy. The development of AKD within the first 3 months of commencing TDF-based therapy was associated with an increase in baseline serum creatinine, age, baseline eGFR and female sex. We concluded that baseline characteristics and baseline renal function biomarkers predicted the risk for AKD within the first 3-months of TDF-based therapy.

Identifiants

pubmed: 34252117
doi: 10.1371/journal.pone.0252768
pii: PONE-D-21-09516
pmc: PMC8274919
doi:

Substances chimiques

Tenofovir 99YXE507IL

Banques de données

Dryad
['10.5061/dryad.51c59zw88']

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0252768

Subventions

Organisme : FIC NIH HHS
ID : D43 TW009744
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK114809
Pays : United States

Déclaration de conflit d'intérêts

NO authors have competing interests. EDS reports consulting for Akebia, Inc. 4/19, honorarium for an invited educational talk at the Annual Da Vita Physician Leadership Conference 2/19, royalties as an author for UpToDate, and serving on the editorial board for the Clinical Journal of the American Society of Nephrology. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Freeman W Chabala (FW)

Levy Mwanawasa Medical University, Institute of Basic and Biomedical Sciences, Lusaka, Zambia.
The University of Zambia, School of Medicine, Lusaka, Zambia.

Edward D Siew (ED)

Vanderbilt University Medical Center, Division of Nephrology and Hypertension, Vanderbilt O'Brien Center for Kidney Disease, Nashville, Tennessee, United States of America.
Tennessee Valley Health Systems (TVHS), Veterans Affairs, Nashville, TN, United States of America.

Wilbroad Mutale (W)

The University of Zambia, School of Public Health, Lusaka, Zambia.
Vanderbilt Institute for Global Health, Vanderbilt University Medical Center, Nashville, TN, United States of America.

Lloyd Mulenga (L)

The University of Zambia, School of Medicine, Lusaka, Zambia.
Vanderbilt University Medical Center, Division of Nephrology and Hypertension, Vanderbilt O'Brien Center for Kidney Disease, Nashville, Tennessee, United States of America.
Vanderbilt Institute for Global Health, Vanderbilt University Medical Center, Nashville, TN, United States of America.

Aggrey Mweemba (A)

The University of Zambia, School of Medicine, Lusaka, Zambia.
The University Teaching Hospital, Lusaka, Zambia.

Fastone Goma (F)

The University of Zambia, School of Medicine, Lusaka, Zambia.

Njeleka Banda (N)

The University Teaching Hospital, Lusaka, Zambia.

Patrick Kaonga (P)

Vanderbilt University Medical Center, Division of Nephrology and Hypertension, Vanderbilt O'Brien Center for Kidney Disease, Nashville, Tennessee, United States of America.

William C Wester (WC)

Vanderbilt University Medical Center, Division of Nephrology and Hypertension, Vanderbilt O'Brien Center for Kidney Disease, Nashville, Tennessee, United States of America.
The University Teaching Hospital, Lusaka, Zambia.

Douglas C Heimburger (DC)

The University of Zambia, School of Medicine, Lusaka, Zambia.
Vanderbilt University Medical Center, Division of Nephrology and Hypertension, Vanderbilt O'Brien Center for Kidney Disease, Nashville, Tennessee, United States of America.
Vanderbilt Institute for Global Health, Vanderbilt University Medical Center, Nashville, TN, United States of America.

Muktar H Aliyu (MH)

Vanderbilt University Medical Center, Division of Nephrology and Hypertension, Vanderbilt O'Brien Center for Kidney Disease, Nashville, Tennessee, United States of America.
Vanderbilt Institute for Global Health, Vanderbilt University Medical Center, Nashville, TN, United States of America.
Meharry Medical College School of Medicine, Nashville, TN, United States of America.

Derick Munkombwe (D)

The University of Zambia, School of Health Sciences, Lusaka, Zambia.

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