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dc.contributor.authorAngwe, Martin Kamilo
dc.date.accessioned2024-01-17T08:58:20Z
dc.date.available2024-01-17T08:58:20Z
dc.date.issued2023
dc.identifier.citationAngwe, M. K. (2023). Artemether-Lumefantrine Plasmodium Falciparum clearance and associated factors among uncomplicated Malaria patients in Adjumani District, Uganda (Unpublished master's dissertation). Makerere University, Kampala, Ugandaen_US
dc.identifier.urihttp://hdl.handle.net/10570/13060
dc.descriptionA dissertation submitted to the Directorate of Research and Graduate Training in partial fulfilment of the requirements for the award of the Degree of Master of Science in Pharmacology of Makerere University.en_US
dc.description.abstractThe development of artemisinin resistance threatens the efforts to global malaria control. Artemisinin resistance has been reported in Northern Uganda and some African countries. Considering both host and parasite genetic factors to adequately understand and monitor the emerging threat and the spread of artemisinin resistance is vital. This longitudinal study recruited 100 symptomatic malaria patients aged five and above; who had P. falciparum infection and were prescribed artemether-lumefantrine. Microscopy and qPCR were used to determine day 0 and day 3 parasitemia. 80 Parasite DNA were sequenced for mutation in the K13-propeller gene using Sanger sequencing. The prevalence of human CYP2B6*6 allele was determined by Restricted Fragment Length Polymorphism using the patient's DNA (100). Sequence data was analysed by MEGA11 and processed in Excel and STATA15 with the rest, a Mann-Whitney U test was used to compare parasite clearance. 63% of patients had detectable parasites by qPCR and 24% by microscopy at day 3. Polymorphism in the P. falciparum K13-propeller gene was detected in 15 of the 80 samples sequenced. The K13 mutations found were C469Y (12.5%, 10/80), A675V (2.5%, 2/80), A569S (1.25%, 1/80), A578S (1.25%, 1/80), and F491S (1.25%, 1/80), C469Y demonstrated low parasite clearance (P=0.03). Genotype frequency for human CYP2B6*6 was 43% GG, 17% TT and 40% GT. GT patients showed reduced parasite clearance compared to GG and TT (P=0.02). Conclusion and Recommendation: There is an increase in the prevalence of Day 3 Plasmodium falciparum in AL-treated patients. Parasite K13 mutations, candidates of artemisinin resistance, were detected in parasites isolated from the patients. There is interindividual variability in the patient CYP2B6*6 gene. Parasite K13 mutation and patients' CYP2B6*6 variability affect parasite clearance. There is a need to re-evaluate the efficacy of artemisinin agents in malaria treatment in the country, considering both host and parasite factors, and alternative treatment approaches should be intensified.en_US
dc.description.sponsorshipThis study was supported by funding through the EDCTP2 programme supported by the European Union (TMA2019CDF-2662-Pfkelch13 emergence) and Fogarty International Center of the National Institute of Health under award number 1R25TW011213.en_US
dc.language.isoenen_US
dc.publisherMakerere Universityen_US
dc.subjectArtemisinin resistanceen_US
dc.subjectMalaria controlen_US
dc.subjectPlasmodium falciparumen_US
dc.subjectMutationen_US
dc.subjectGenotypesen_US
dc.subjectAllelesen_US
dc.subjectK13en_US
dc.subjectCYP2B6*6en_US
dc.titleArtemether-Lumefantrine Plasmodium Falciparum clearance and associated factors among uncomplicated Malaria patients in Adjumani District, Ugandaen_US
dc.typeThesisen_US


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