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

Author:

Kiiza Daniel1ORCID,Rostami-Hochaghan Danial2,Alhassan Yussif3,Seden Kay2,Reynolds Helen2,Kaboggoza Julian P1,Taegtmeyer Miriam3,Chen Tao3,Challenger Elizabeth2,Malaba Thokozile4,Wang Duolao3,Else Laura2,Hern Faye5,Sharp Jo2,Neary Megan2ORCID,Dilly Penchala Sujan2,Waitt Catriona12,Orrell Catherine6,Colbers Angela7ORCID,Myer Landon3,Owen Andrew2ORCID,Rannard Steve5,Khoo Saye28ORCID,Lamorde Mohammed1

Affiliation:

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

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

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

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

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

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

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

8. Royal Liverpool University Hospital , NHS Trust , UK

Abstract

Abstract 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 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 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 The widespread use of clay-based TM may compromise HIV treatment, necessitating medication screening and counselling to manage DDIs in pregnant women.

Funder

Unitaid

ViiV Healthcare

Publisher

Oxford University Press (OUP)

Reference32 articles.

1. Achieving UNAIDS 90-90-90 targets for pregnant and postpartum women in sub-Saharan Africa: progress, gaps and research needs;Abuogi;J Virus Erad,2018

2. Early initiation of ARV during pregnancy to move towards virtual elimination of mother-to-child-transmission of HIV-1 in Yunnan, China;Meyers;PLoS One,2015

3. Prevalence and type of drug–drug interactions involving ART in patients attending a specialist HIV outpatient clinic in Kampala, Uganda;Seden;J Antimicrob Chemother,2015

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