Evidence map›Paper›PMID 41998533›Full record

ArticleBMC infectious diseases2026

Characterisation of malaria and glucose-6-phosphate dehydrogenase deficiency in conflict-affected zones of southern and eastern Sudan.

Waleed M A Jebreel, Muzamil M Abdel Hamid, Sayed A Mustafa, Fahad Awad, Martin Chamai, Kenny Malpartida-Cardenas, Elaine Asiwome Boadu, Linda Eva Amoah, Jesus Rodriguez-Manzano, Aubrey J Cunnington and 2 more

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Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Waleed M A JebreelInstitute of Endemic Diseases, University of Khartoum, Khartoum, Sudan. waleedalhaj@iend.org.ORCID http://orcid.org/0000-0002-8107-4153
Muzamil M Abdel HamidDepartment of Parasitology and Medical Entomology, Institute of Endemic Diseases, University of Khartoum, Khartoum, Sudan. mahdi@iend.org.ORCID http://orcid.org/0000-0002-6157-4388
Sayed A MustafaMalaria Control Program, Federal Ministry of Health, Khartoum, Sudan.
Fahad AwadMalaria Control Program, Federal Ministry of Health, Khartoum, Sudan.
Martin ChamaiWest African Center for Cell Biology of Infectious Pathogens, University of Ghana, Accra, Ghana.
Kenny Malpartida-CardenasDepartment of Infectious Diseases, Faculty of Medicine, Imperial College London, London, UK.
Elaine Asiwome BoaduNoguchi Memorial Institute for Medical Research, University of Ghana, Legon, Ghana.
Linda Eva AmoahNoguchi Memorial Institute for Medical Research, University of Ghana, Legon, Ghana.
Jesus Rodriguez-ManzanoDepartment of Infectious Diseases, Faculty of Medicine, Imperial College London, London, UK.
Aubrey J CunningtonThe Fleming Initiative, Imperial College London, London, UK.
Abdelrahim O MohamedInstitute of Endemic Diseases, University of Khartoum, Khartoum, Sudan. Abdelrahim_osman@yahoo.com.
NIHR Global Health Research Group on Digital Diagnostics for African Health Systems

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMalaria causes high morbidity and mortality in Sudan. Malaria control efforts have been disrupted by conflict and displacement, which affected the whole health system. This study aimed to characterize malaria and glucose-6-phosphate dehydrogenase deficiency in conflict-affected zones of southern and eastern Sudan.

methodsThis cross-sectional study was conducted between 2023 and 2024, enrolling 717 patients with clinical symptoms suggestive of malaria in Kosti (southern Sudan, n = 252) and Kassala (Eastern Sudan, n = 465). Malaria infection was confirmed by light microscopy as a standard test, and qPCR was used as a reference method. Haematological indices were analysed on automated analysers, and PCR-RFLP was used to determine G6PD genotypes.

resultsMalaria prevalence was 62.6% (291/465; 95% CI 58.2–67.0%) in Kassala and 52% (133/252; 95% CI 46.6–59.0%) in Kosti using PCR. In Kassala, 157 cases (54%; 95% CI: 48.2–59.7%) were Plasmodium vivax (P.v), 99 (34%; 95% CI: 28.6–39.8%) were Plasmodium falciparum (P. f), and 35 (12%; 95% CI: 8.6–16.2%) were P. f/P. v infections. In Kosti, P. f was detected in 130 (97.7%) subjects, and P. v was detected in 3 (2.7%; all were negative by microscopy). There were 37 (8.7%) subjects not detected by microscopy but positive by PCR (submicroscopic), 20 (15%) in Kosti and 17 (5.8%) in Kassala. The G6PD B variant predominated in Kassala (438/94.2%) and Kosti (200/79.4%). The African A− variant was detected in 9 (3.5%) individuals in Kosti (7 males, 2 females). In Kosti females, BA, BA−, AA, and AA− were observed in 11 (7%), 4 (2.5%), 4 (2.5%), and 9 (5.7%), respectively, compared to 10 (4.1%), 4 (1.6%), and 7 (3%) BA, BA−, and AA cases in Kassala females. No significant association was observed between G6PD genotype and parasite density. Malaria prevalence did not differ significantly between Internally Displaced Persons (IDPs) and residents.

conclusionsRegional variation was observed in malaria parasite species, including submicroscopic infections, as well as in G6PD genotypes. The study identified the G6PD A− variant in Sudan. Ongoing conflict in Sudan has similarly impacted the health of both resident and displaced populations. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Glucosephosphate Dehydrogenase DeficiencyMalariaMalaria, FalciparumMalaria, VivaxAdolescentAdultChildChild, PreschoolCross-Sectional StudiesFemaleGenotypeGlucosephosphate DehydrogenaseHumansInfantMaleMiddle AgedGlucosephosphate DehydrogenaseConflict settingG6PD deficiencyInternally displaced persons (IDPs)MalariaPlasmodium falciparumPlasmodium vivaxSub-microscopic infectionSudan

Identifiers

PMID41998533
PMCPMC13224569

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.