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How has mass drug administration with dihydroartemisinin-piperaquine impacted molecular markers of drug resistance? A systematic review.

Moss, S; Mańko, E; Krishna, S; Campino, S; Clark, TG; Last, A (2022) How has mass drug administration with dihydroartemisinin-piperaquine impacted molecular markers of drug resistance? A systematic review. Malar J, 21 (1). p. 186. ISSN 1475-2875 https://doi.org/10.1186/s12936-022-04181-y
SGUL Authors: Krishna, Sanjeev

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Abstract

The World Health Organization (WHO) recommends surveillance of molecular markers of resistance to anti-malarial drugs. This is particularly important in the case of mass drug administration (MDA), which is endorsed by the WHO in some settings to combat malaria. Dihydroartemisinin-piperaquine (DHA-PPQ) is an artemisinin-based combination therapy which has been used in MDA. This review analyses the impact of MDA with DHA-PPQ on the evolution of molecular markers of drug resistance. The review is split into two parts. Section I reviews the current evidence for different molecular markers of resistance to DHA-PPQ. This includes an overview of the prevalence of these molecular markers in Plasmodium falciparum Whole Genome Sequence data from the MalariaGEN Pf3k project. Section II is a systematic literature review of the impact that MDA with DHA-PPQ has had on the evolution of molecular markers of resistance. This systematic review followed PRISMA guidelines. This review found that despite being a recognd surveillance tool by the WHO, the surveillance of molecular markers of resistance following MDA with DHA-PPQ was not commonly performed. Of the total 96 papers screened for eligibility in this review, only 20 analysed molecular markers of drug resistance. The molecular markers published were also not standardized. Overall, this warrants greater reporting of molecular marker prevalence following MDA implementation. This should include putative pfcrt mutations which have been found to convey resistance to DHA-PPQ in vitro.

Item Type: Article
Additional Information: © The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Keywords: Antimalarial resistance, Dihydroartemisinin-piperaquine, Mass drug administration, Molecular markers, Antimalarials, Artemisinins, Biomarkers, Drug Resistance, Humans, Malaria, Falciparum, Mass Drug Administration, Piperazines, Plasmodium falciparum, Quinolines, Humans, Plasmodium falciparum, Malaria, Falciparum, Artemisinins, Piperazines, Quinolines, Antimalarials, Drug Resistance, Biomarkers, Mass Drug Administration, 0605 Microbiology, 1108 Medical Microbiology, 1117 Public Health and Health Services, Tropical Medicine
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Malar J
ISSN: 1475-2875
Language: eng
Dates:
DateEvent
11 June 2022Published
10 May 2022Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
MR/N013638/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/N010469/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/M01360X/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/R025576/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/R020973/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/S005013/1Joint Global Health Trials SchemeUNSPECIFIED
PubMed ID: 35690758
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/114490
Publisher's version: https://doi.org/10.1186/s12936-022-04181-y

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