Evidence map›Paper›PMID 36207750›Full record

ArticleMalaria journal2022

High prevalence of Pfcrt 76T and Pfmdr1 N86 genotypes in malaria infected patients attending health facilities in East Shewa zone, Oromia Regional State, Ethiopia.

Jifar Hassen, Gezahegn Solomon Alemayehu, Hunduma Dinka, Lemu Golassa

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In one paragraph

Article in Malaria journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.0field-weighted citation impact, top 4% of its field
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 26 citations in OpenAlex.

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  16. Pathogens (Basel, Switzerland) · 2023
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4 · The record

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5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Jifar HassenDepartment of Applied Biology, School of Applied Natural Science, Adama Science and Technology University, P. O. Box 1888, Adama, Ethiopia. jifarhassen18@gmail.com.
Gezahegn Solomon AlemayehuResearch and Community Service Center, College of Health Science, Defense University, P. O. Box 1419, Bishoftu, Ethiopia.
Hunduma DinkaDepartment of Applied Biology, School of Applied Natural Science, Adama Science and Technology University, P. O. Box 1888, Adama, Ethiopia.
Lemu GolassaAklilu Lemma Institute of Pathobiology, Addis Ababa University, P. O. Box 1176, Addis Ababa, Ethiopia.
Adama Science and Technology University · ETAddis Ababa University · ETDefence University College · ET

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundPlasmodium falciparum resistance to series of anti-malarial drugs is a major challenge in efforts to control and/or eliminate malaria globally. In 1998, following the widespread of chloroquine (CQ) resistant P. falciparum, Ethiopia switched from CQ to sulfadoxine-pyrimethamine (SP) and subsequently in 2004 from SP to artemether-lumefantrine (AL) for the treatment of uncomplicated falciparum malaria. Data on the prevalence of CQ resistance markers after more than two decades of its removal is important to map the selection pressure behind the targets codons of interest. The present study was conducted to determine the prevalence of mutations in Pfcrt K76T and Pfmdr1 N86Y codons among malaria-infected patients from Adama, Olenchiti and Metehara sites of East Shewa zone, Oromia Regional State, Ethiopia.

methodsFinger-prick whole blood samples were collected on 3MM Whatman ® filter papers from a total of 121 microscopically confirmed P. falciparum infected patients. Extraction of parasite DNA was done by Chelex-100 method from dried blood spot (DBS). Genomic DNA template was used to amplify Pfcrt K76T and Pfmdr1 N86Y codons by nested PCR. Nested PCR products were subjected to Artherobacter protophormiae-I (APoI) restriction enzyme digestion to determine mutations at codons 76 and 86 of Pfcrt and Pfmdr1 genes, respectively.

resultsOf 83 P. falciparum isolates successfully genotyped for Pfcrt K76T, 91.6% carried the mutant genotypes (76T). The prevalence of Pfcrt 76T was 95.7%, 92.5% and 84.5% in Adama, Metehara and Olenchiti, respectively. The prevalence of Pfcrt 76T mutations in three of the study sites showed no statistical significance difference (χ

conclusionAlthough CQ officially has been ceased for the treatment of falciparum malaria for more than two decades in Ethiopia, greater proportions of P. falciparum clinical isolates circulating in the study areas carry the mutant 76T genotypes indicating the presence of indirect CQ pressure in the country. However, the return of Pfmdr1 N86 wild-type allele may be favoured by the use of AL for the treatment of uncomplicated falciparum malaria.

Indexed as

AntimalarialsMalariaMalaria, FalciparumArtemetherArtemether, Lumefantrine Drug CombinationATP-Binding Cassette, Sub-Family C ProteinsChloroquineDrug ResistanceEthiopiaGenotypeHealth FacilitiesHumansPlasmodium falciparumPrevalenceProtozoan ProteinsAntimalarialsArtemetherArtemether, Lumefantrine Drug CombinationATP-Binding Cassette, Sub-Family C ProteinsChloroquineProtozoan ProteinsAnti-malarial drug resistanceEthiopiaPfcrtPfmdr1Plasmodium falciparum

Identifiers

PMID36207750
PMCPMC9547420
OpenAlexW4303446471

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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 OpenQuestion graph.