Tenofovir diphosphate in dried blood spots predicts future viremia in persons with HIV taking antiretroviral therapy in South Africa.


Journal

AIDS (London, England)
ISSN: 1473-5571
Titre abrégé: AIDS
Pays: England
ID NLM: 8710219

Informations de publication

Date de publication:
01 06 2022
Historique:
pubmed: 9 2 2022
medline: 7 6 2022
entrez: 8 2 2022
Statut: ppublish

Résumé

Tenofovir diphosphate (TFV-DP) in dried blood spots (DBS) is used as a biomarker of antiretroviral therapy (ART) adherence. Recent treatment studies have shown that TFV-DP predicts future viremia in persons with HIV (PWH) but there are few data from high-burden settings. We investigated whether TFV-DP in DBS predicts future viral breakthrough in South African PWH. Prospective observational cohort. We enrolled 250 adults receiving tenofovir-containing regimens, currently virally suppressed (<50 copies/ml) but at risk of future viral breakthrough, from four primary health clinics in Cape Town. Paired viral load and DBS for TFV-DP were collected monthly for 12 months. Viral breakthrough was the first confirmed viral load greater than 400 copies/ml. Logistic regression estimated the odds ratio (OR) and 95% confidence intervals for future viral breakthrough at the next visit. Participants provided 2944 paired DBS and viral load samples. Median (IQR) age was 34 (27-42) years; median duration on ART at study entry was 11 (4-12) months;78% were women. Twenty-one (8%) participants developed viral breakthrough. Participants with TFV-DP 400 fmol/punch or less had an adjusted OR of 16.1 (95% CI: 3.9-67.4; P < 0.001) for developing viral breakthrough 1 month later compared with participants with TFV-DP greater 800 fmol/punch. TFV-DP in DBS strongly predicted future viral breakthrough in a clinical cohort of South African PWH. A biomarker able to identify PWH at risk for future viral breakthrough has the potential to improve health outcomes through timely intervention. Future studies exploring the clinical use of TFV-DP in DBS in conjunction with viral load in ART monitoring are warranted.

Identifiants

pubmed: 35131960
doi: 10.1097/QAD.0000000000003185
pii: 00002030-202206010-00003
pmc: PMC9167214
mid: NIHMS1777883
doi:

Substances chimiques

Anti-HIV Agents 0
Biomarkers 0
Organophosphates 0
tenofovir diphosphate 0
Adenine JAC85A2161

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

933-940

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI122300
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc.

Références

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Auteurs

Lauren Jennings (L)

Desmond Tutu Health Foundation, Cape Town, South Africa.

Reuben N Robbins (RN)

New York State Psychiatric Institute.

Nadia Nguyen (N)

Columbia University.

Christopher Ferraris (C)

New York State Psychiatric Institute.

Cheng-Shiun Leu (CS)

Columbia University Medical Center, New York, New York, USA.

Curtis Dolezal (C)

New York State Psychiatric Institute.

Nei-Yuan Hsiao (NY)

National Health Laboratory Service.
University of Cape Town, Cape Town, South Africa.

Ofole Mgbako (O)

Columbia University Medical Center, New York, New York, USA.

John Joska (J)

University of Cape Town, Cape Town, South Africa.

Jose R Castillo-Mancilla (JR)

University of Colorado, Aurora, Colorado, USA.

Landon Myer (L)

Division of Epidemiology & Biostatistics, School of Public Health & Family Medicine, University of Cape Town, Cape Town, South Africa.

Peter L Anderson (PL)

University of Colorado, Aurora, Colorado, USA.

Robert H Remien (RH)

New York State Psychiatric Institute.

Catherine Orrell (C)

Desmond Tutu Health Foundation, Cape Town, South Africa.

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