Mapping genetic markers of artemisinin resistance in Plasmodium falciparum malaria in Asia: a systematic review and spatiotemporal analysis

dc.contributor.authorKagoro F.M.
dc.contributor.authorBarnes K.I.
dc.contributor.authorMarsh K.
dc.contributor.authorEkapirat N.
dc.contributor.authorMercado C.E.G.
dc.contributor.authorSinha I.
dc.contributor.authorHumphreys G.
dc.contributor.authorDhorda M.
dc.contributor.authorGuerin P.J.
dc.contributor.authorMaude R.J.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-18T17:24:17Z
dc.date.available2023-06-18T17:24:17Z
dc.date.issued2022-03-01
dc.description.abstractBackground: The increase in artemisinin resistance threatens malaria elimination in Asia by the target date of 2030 and could derail control efforts in other endemic regions. This study aimed to develop up-to-date spatial distribution visualisations of the kelch13 (K13) gene markers of artemisinin resistance in Plasmodium falciparum for policy makers. Methods: In this systematic review and spatiotemporal analysis we used the WorldWide Antimalarial Resistance Network (WWARN) surveyor molecular markers of artemisinin resistance database. We updated the database by searching PubMed and SCOPUS for studies published between Jan 1, 1990, and March 31, 2021. Articles were included if they contained data on K13 markers of artemisinin resistance from patients' samples in Asia and articles already included in the WWARN database were excluded. Data were extracted from the published articles and authors were contacted when information was missing. We used the lowest administrative unit levels for the sampling locations of all the K13 data to describe the spatiotemporal distribution. The numbers of samples tested and those with each molecular marker in each administrative unit level were aggregated by year to calculate the marker prevalence over time. Findings: Data were collated from 72 studies comprising K13 markers from 16 613 blood samples collected from 1991 to 2020 from 18 countries. Most samples were from Myanmar (3842 [23·1%]), Cambodia (3804 [22·9%]), and Vietnam (2663 [16·0%]). The median time between data collection and publication was 3·6 years (range 0·9–25·0, IQR 2·7 [2·5–5·2]). There was a steady increase in the prevalence of WHO-validated K13 markers, with the lowest of 4·3% in 2005 (n=47) and the highest of 62·9% in 2018 (n=264). Overall, the prevalence of Cys580Tyr mutation increased from 48·9% in 2002 to 84·9% in 2018. Interpretation: From 2002 to 2018, there has been a steady increase in geographical locations and the proportion of infected people with validated artemisinin resistance markers. More consistent data collection, over more extended periods in the same areas with the rapid sharing of data are needed to map the spread and evolution of resistance to better inform policy decisions. Data in the literature are reported in a heterogeneous way leading to difficulties in pooling and interpretation. We propose here a tool with a set of minimum criteria for reporting future studies. Funding: This research was funded in part by the Wellcome Trust.
dc.identifier.citationThe Lancet Microbe Vol.3 No.3 (2022) , e184-e192
dc.identifier.doi10.1016/S2666-5247(21)00249-4
dc.identifier.eissn26665247
dc.identifier.scopus2-s2.0-85125488703
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/85015
dc.rights.holderSCOPUS
dc.subjectImmunology and Microbiology
dc.titleMapping genetic markers of artemisinin resistance in Plasmodium falciparum malaria in Asia: a systematic review and spatiotemporal analysis
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85125488703&origin=inward
oaire.citation.endPagee192
oaire.citation.issue3
oaire.citation.startPagee184
oaire.citation.titleThe Lancet Microbe
oaire.citation.volume3
oairecerif.author.affiliationInfectious Diseases Data Observatory
oairecerif.author.affiliationWorldWide Antimalarial Resistance Network
oairecerif.author.affiliationFaculty of Tropical Medicine, Mahidol University
oairecerif.author.affiliationHarvard T.H. Chan School of Public Health
oairecerif.author.affiliationThe Open University
oairecerif.author.affiliationNuffield Department of Medicine
oairecerif.author.affiliationUniversity of Cape Town

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