Uncomplicated malaria as a risk factor for COVID-19 duration and severity in western Kenya and Burkina Faso (MALCOV): a prospective cohort study

BACKGROUND: The relationship between malaria and COVID-19 varies across different clinical scenarios; historical malaria exposure might protect against severe COVID-19, whereas co-infection in hospitalised patients with severe disease might increase mortality. Interactions between non-severe malaria and COVID-19 remain poorly understood. We conducted a cohort study among COVID-19 patients of all ages in western Kenya and Burkina Faso to assess the effects of acute, uncomplicated Plasmodium falciparum malaria co-infection on COVID-19 outcomes in ambulatory patients. METHODS: Participants with laboratory-confirmed SARS-CoV-2 infection (positive rapid antigen test or reverse transcription quantitative real-time PCR [RT-qPCR]) were tested for malaria by rapid antigen tests with confirmatory microscopy. Patients with COVID-19 and malaria co-infection received artemether-lumefantrine or pyronaridine-artesunate. COVID-19 symptom course was assessed daily using FLU-PRO Plus (a validated patient-reported outcome instrument) until day 14. Viral load was measured by RT-qPCR on days 0, 3, 7, 14, and 28. The primary endpoint was time to symptom resolution on the FLU-PRO Plus. Analyses were adjusted for country, age, disease severity, and viral load. FINDINGS: =0·042). SARS-CoV-2 clearance was slower in the malaria group by day 7 (aHR 0·69 [95% CI 0·51-0·94]; p=0·017) but was similar between groups by day 28 (adjusted risk ratio 0·99 [95% CI 0·79-1·24]; p=0·95). INTERPRETATION: This study shows that acute uncomplicated malaria co-infection does not adversely affect COVID-19 progression when appropriately treated. Moreover, serological evidence confirms that previous lifelong malaria exposure might provide some protection, with exposed individuals having faster symptom resolution. FUNDING: Gates Foundation. TRANSLATION: For the French translation of the abstract see Supplementary Materials section.

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Journal
The Lancet Global Health
Published
2026-04-15
DOI
https://doi.org/10.1016/s2214-109x(25)00541-8
Primary Topic
Malaria Research and Control
Type
article
Field-Weighted Citation Impact
0.00

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article

Uncomplicated malaria as a risk factor for COVID-19 duration and severity in western Kenya and Burkina Faso (MALCOV): a prospective cohort study

Alphonse Ouédraogo, Julian Matthewman, Everlyne Delylah Ondieki, Tegwen Marlais et al.
The Lancet Global Health
Malaria Research and Control
article

Uncomplicated malaria as a risk factor for COVID-19 duration and severity in western Kenya and Burkina Faso (MALCOV): a prospective cohort study

Alphonse Ouédraogo, Julian Matthewman, Everlyne Delylah Ondieki, Tegwen Marlais, Maia Lesosky, Issiaka Soulama, Aïssata Barry, Emilie S. Badoum, Jennifer Canizales, David J. Allen, Hellen C. Barsosio, Ben Idriss Soulama, Brian Tangara, Morine Achieng, Helena Brazal-Monzó, Anna Drabko, Luke Hannan, Telesphorus Odawo, Miriam Wanjiku, Henry Aura, Sodiomon B. Sirima, Jean Moïse T Kaboré, Chris Drakeley, Alfred B Tiono, Samuel S Serme, Kevin K A Tetteh, William Wu, Kephas Otieno, Eric D Onyango, Simon Kariuki, Feiko O ter Kuile
article en

Abstract

BACKGROUND: The relationship between malaria and COVID-19 varies across different clinical scenarios; historical malaria exposure might protect against severe COVID-19, whereas co-infection in hospitalised patients with severe disease might increase mortality. Interactions between non-severe malaria and COVID-19 remain poorly understood. We conducted a cohort study among COVID-19 patients of all ages in western Kenya and Burkina Faso to assess the effects of acute, uncomplicated Plasmodium falciparum malaria co-infection on COVID-19 outcomes in ambulatory patients. METHODS: Participants with laboratory-confirmed SARS-CoV-2 infection (positive rapid antigen test or reverse transcription quantitative real-time PCR [RT-qPCR]) were tested for malaria by rapid antigen tests with confirmatory microscopy. Patients with COVID-19 and malaria co-infection received artemether-lumefantrine or pyronaridine-artesunate. COVID-19 symptom course was assessed daily using FLU-PRO Plus (a validated patient-reported outcome instrument) until day 14. Viral load was measured by RT-qPCR on days 0, 3, 7, 14, and 28. The primary endpoint was time to symptom resolution on the FLU-PRO Plus. Analyses were adjusted for country, age, disease severity, and viral load. FINDINGS: =0·042). SARS-CoV-2 clearance was slower in the malaria group by day 7 (aHR 0·69 [95% CI 0·51-0·94]; p=0·017) but was similar between groups by day 28 (adjusted risk ratio 0·99 [95% CI 0·79-1·24]; p=0·95). INTERPRETATION: This study shows that acute uncomplicated malaria co-infection does not adversely affect COVID-19 progression when appropriately treated. Moreover, serological evidence confirms that previous lifelong malaria exposure might provide some protection, with exposed individuals having faster symptom resolution. FUNDING: Gates Foundation. TRANSLATION: For the French translation of the abstract see Supplementary Materials section.

The Lancet Global HealthVol. 14(5)
University of London (GB), Liverpool School of Tropical Medicine (GB), Kenya Medical Research Institute (KE), London School of Hygiene & Tropical Medicine (GB), Quantitative BioSciences (US), Lung Institute (US), Groupe de Recherche et d’Action sur le Foncier (BF), Institut de Recherche en Sciences de la Santé (BF)
Bill and Melinda Gates Foundation
Good health and well-being
Openalex Percentile: Top 22%
Malaria Research and Control
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