Clinical, pharmacological, and qualitative characterization of drug-drug interactions in pregnant women initiating HIV therapy in Sub-Saharan Africa.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
13 Jul 2024
Historique:
received: 01 12 2023
accepted: 22 06 2024
medline: 13 7 2024
pubmed: 13 7 2024
entrez: 12 7 2024
Statut: aheadofprint

Résumé

We investigated the impact of Drug-Drug Interactions (DDIs) on virologic control among HIV-positive pregnant women initiating antiretroviral therapy while identifying drivers for Traditional Medicine (TM) use and exploring the nature and extent of TM-related DDIs. Employing a three-pronged approach, we examined DDIs arising from comedication, including TM, in ART. The DolPHIN-2 trial (NCT03249181) randomized 268 HIV-positive pregnant women in Uganda and South Africa to dolutegravir (DTG)-based (135) or efavirenz-based (133) regimens while systematically recording comedications and screening for DDIs. We used Cox regression models to compare time-to-virologic control between participants with and without DDIs. We conducted in-depth interviews and focus group discussions among 37 and 67 women with and without HIV, respectively, to explore reasons for TM use during pregnancy. Additionally, in-vitro and in-vivo studies evaluated the composition and impact of clay-based TM, mumbwa, on DTG plasma exposure. The baseline prevalence of DDIs was 67.2%, with TM use prevalent in 34% of participants, with mumbwa being the most frequent (76%, 69/91). There was no difference in virologic response between participants with and without DDIs. Fetal health and cultural norms were among the reasons cited for TM use. Analysis of mumbwa rods confirmed significant amounts of aluminium (8.4%-13.9%) and iron (4%-6%). In Balb-C mice, coadministration of mumbwa led to a reduction in DTG exposure observed in the AUC0-24 (-21%; P = 0.0271) and C24 (-53%; P = 0.0028). The widespread use of clay-based TM may compromise HIV treatment, necessitating medication screening and counselling to manage DDIs in pregnant women.

Sections du résumé

BACKGROUND BACKGROUND
We investigated the impact of Drug-Drug Interactions (DDIs) on virologic control among HIV-positive pregnant women initiating antiretroviral therapy while identifying drivers for Traditional Medicine (TM) use and exploring the nature and extent of TM-related DDIs.
METHODS METHODS
Employing a three-pronged approach, we examined DDIs arising from comedication, including TM, in ART. The DolPHIN-2 trial (NCT03249181) randomized 268 HIV-positive pregnant women in Uganda and South Africa to dolutegravir (DTG)-based (135) or efavirenz-based (133) regimens while systematically recording comedications and screening for DDIs. We used Cox regression models to compare time-to-virologic control between participants with and without DDIs. We conducted in-depth interviews and focus group discussions among 37 and 67 women with and without HIV, respectively, to explore reasons for TM use during pregnancy. Additionally, in-vitro and in-vivo studies evaluated the composition and impact of clay-based TM, mumbwa, on DTG plasma exposure.
RESULTS RESULTS
The baseline prevalence of DDIs was 67.2%, with TM use prevalent in 34% of participants, with mumbwa being the most frequent (76%, 69/91). There was no difference in virologic response between participants with and without DDIs. Fetal health and cultural norms were among the reasons cited for TM use. Analysis of mumbwa rods confirmed significant amounts of aluminium (8.4%-13.9%) and iron (4%-6%). In Balb-C mice, coadministration of mumbwa led to a reduction in DTG exposure observed in the AUC0-24 (-21%; P = 0.0271) and C24 (-53%; P = 0.0028).
CONCLUSIONS CONCLUSIONS
The widespread use of clay-based TM may compromise HIV treatment, necessitating medication screening and counselling to manage DDIs in pregnant women.

Identifiants

pubmed: 38997229
pii: 7713049
doi: 10.1093/jac/dkae232
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Unitaid
Organisme : ViiV Healthcare

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Daniel Kiiza (D)

Research Department, Infectious Diseases Institute, College of Health Sciences, Makerere University, Kampala, Uganda.

Danial Rostami-Hochaghan (D)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Yussif Alhassan (Y)

Department of International Public Health, Liverpool School of Tropical Medicine, Liverpool, UK.

Kay Seden (K)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Helen Reynolds (H)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Julian P Kaboggoza (JP)

Research Department, Infectious Diseases Institute, College of Health Sciences, Makerere University, Kampala, Uganda.

Miriam Taegtmeyer (M)

Department of International Public Health, Liverpool School of Tropical Medicine, Liverpool, UK.

Tao Chen (T)

Department of International Public Health, Liverpool School of Tropical Medicine, Liverpool, UK.

Elizabeth Challenger (E)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Thokozile Malaba (T)

Division of Epidemiology and Biostatistics, School of Public Health, University of Cape Town, Cape Town, South Africa.

Duolao Wang (D)

Department of International Public Health, Liverpool School of Tropical Medicine, Liverpool, UK.

Laura Else (L)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Faye Hern (F)

Department of Chemistry, University of Liverpool, Liverpool, UK.

Jo Sharp (J)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Megan Neary (M)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Sujan Dilly Penchala (S)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Catriona Waitt (C)

Research Department, Infectious Diseases Institute, College of Health Sciences, Makerere University, Kampala, Uganda.
Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Catherine Orrell (C)

Desmond Tutu HIV Centre, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South Africa.

Angela Colbers (A)

Department of Pharmacy, Radboud Institute for Medical Innovations (RIMI), Radboud University Medical Center, Nijmegen, Netherlands.

Landon Myer (L)

Department of International Public Health, Liverpool School of Tropical Medicine, Liverpool, UK.

Andrew Owen (A)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Steve Rannard (S)

Department of Chemistry, University of Liverpool, Liverpool, UK.

Saye Khoo (S)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
Royal Liverpool University Hospital, NHS Trust, UK.

Mohammed Lamorde (M)

Research Department, Infectious Diseases Institute, College of Health Sciences, Makerere University, Kampala, Uganda.

Classifications MeSH