Loading…
Antimalarial Drug Resistance: A Threat to Malaria Elimination
Increasing antimalarial drug resistance once again threatens effective antimalarial drug treatment, malaria control, and elimination. Artemisinin combination therapies (ACTs) are first-line treatment for uncomplicated falciparum malaria in all endemic countries, yet partial resistance to artemisinin...
Saved in:
Published in: | Cold Spring Harbor perspectives in medicine 2017-07, Vol.7 (7), p.a025619 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c439t-799b5f9d2728c4e56b853cabc0f473f1019d15c24ed1a45698d5f4cbabb459ca3 |
---|---|
cites | cdi_FETCH-LOGICAL-c439t-799b5f9d2728c4e56b853cabc0f473f1019d15c24ed1a45698d5f4cbabb459ca3 |
container_end_page | |
container_issue | 7 |
container_start_page | a025619 |
container_title | Cold Spring Harbor perspectives in medicine |
container_volume | 7 |
creator | Menard, Didier Dondorp, Arjen |
description | Increasing antimalarial drug resistance once again threatens effective antimalarial drug treatment, malaria control, and elimination. Artemisinin combination therapies (ACTs) are first-line treatment for uncomplicated falciparum malaria in all endemic countries, yet partial resistance to artemisinins has emerged in the Greater Mekong Subregion. Concomitant emergence of partner drug resistance is now causing high ACT treatment failure rates in several areas. Genetic markers for artemisinin resistance and several of the partner drugs have been established, greatly facilitating surveillance. Single point mutations in the gene coding for the Kelch propeller domain of the K13 protein strongly correlate with artemisinin resistance. Novel regimens and strategies using existing antimalarial drugs will be needed until novel compounds can be deployed. Elimination of artemisinin resistance will imply elimination of all falciparum malaria from the same areas. In vivax malaria, chloroquine resistance is an increasing problem. |
doi_str_mv | 10.1101/cshperspect.a025619 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5495053</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1877526916</sourcerecordid><originalsourceid>FETCH-LOGICAL-c439t-799b5f9d2728c4e56b853cabc0f473f1019d15c24ed1a45698d5f4cbabb459ca3</originalsourceid><addsrcrecordid>eNpdUVFLwzAQDqK4MfcLBOmjPnQmadI0gkKZ0wkTQeZzSNN0i3TtTNKB_96MzTG9lxx33_fdXT4ALhEcIQTRrXLLtbZurZUfSYhpivgJ6GPCcEwJwqchR5TFiGDcA0PnPmEImqYZg-eghzOccUyyPrjPG29WspbWyDp6tN0ietfOOC8bpe-iPJovrZY-8m30ukNFk9qsTCO9aZsLcFbJ2unh_h2Aj6fJfDyNZ2_PL-N8FiuScB8zzgta8RIznCmiaVpkNFGyULAiLKnCPbxEVGGiSyQJTXlW0oqoQhYFoVzJZAAedrrrrljpUunGW1mLtQ2r22_RSiP-dhqzFIt2IyjhFNIkCNzsBJb_aNN8Jra18IWUJ5BvUMBe74fZ9qvTzouVcUrXtWx02zmBMsYoTjlKAzTZQZVtnbO6OmgjKLY-iSOfxN6nwLo6vubA-XUl-QEFypG0</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1877526916</pqid></control><display><type>article</type><title>Antimalarial Drug Resistance: A Threat to Malaria Elimination</title><source>PubMed Central</source><creator>Menard, Didier ; Dondorp, Arjen</creator><creatorcontrib>Menard, Didier ; Dondorp, Arjen</creatorcontrib><description>Increasing antimalarial drug resistance once again threatens effective antimalarial drug treatment, malaria control, and elimination. Artemisinin combination therapies (ACTs) are first-line treatment for uncomplicated falciparum malaria in all endemic countries, yet partial resistance to artemisinins has emerged in the Greater Mekong Subregion. Concomitant emergence of partner drug resistance is now causing high ACT treatment failure rates in several areas. Genetic markers for artemisinin resistance and several of the partner drugs have been established, greatly facilitating surveillance. Single point mutations in the gene coding for the Kelch propeller domain of the K13 protein strongly correlate with artemisinin resistance. Novel regimens and strategies using existing antimalarial drugs will be needed until novel compounds can be deployed. Elimination of artemisinin resistance will imply elimination of all falciparum malaria from the same areas. In vivax malaria, chloroquine resistance is an increasing problem.</description><identifier>ISSN: 2157-1422</identifier><identifier>EISSN: 2472-5412</identifier><identifier>DOI: 10.1101/cshperspect.a025619</identifier><identifier>PMID: 28289248</identifier><language>eng</language><publisher>United States: Cold Spring Harbor Laboratory Press</publisher><subject>Antigens, Bacterial ; Antigens, Bacterial - genetics ; Antigens, Surface ; Antigens, Surface - genetics ; Antimalarials ; Antimalarials - pharmacology ; Artemisinins ; Artemisinins - pharmacology ; Drug Resistance ; Drug Resistance - genetics ; Drug Therapy, Combination ; Human health and pathology ; Humans ; Infectious diseases ; Life Sciences ; Malaria, Falciparum ; Malaria, Falciparum - drug therapy ; Malaria, Vivax ; Malaria, Vivax - drug therapy ; Plasmodium ; Plasmodium - drug effects ; Plasmodium - genetics</subject><ispartof>Cold Spring Harbor perspectives in medicine, 2017-07, Vol.7 (7), p.a025619</ispartof><rights>Copyright © 2017 Cold Spring Harbor Laboratory Press; all rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-799b5f9d2728c4e56b853cabc0f473f1019d15c24ed1a45698d5f4cbabb459ca3</citedby><cites>FETCH-LOGICAL-c439t-799b5f9d2728c4e56b853cabc0f473f1019d15c24ed1a45698d5f4cbabb459ca3</cites><orcidid>0000-0003-1357-4495</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5495053/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5495053/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28289248$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02559309$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Menard, Didier</creatorcontrib><creatorcontrib>Dondorp, Arjen</creatorcontrib><title>Antimalarial Drug Resistance: A Threat to Malaria Elimination</title><title>Cold Spring Harbor perspectives in medicine</title><addtitle>Cold Spring Harb Perspect Med</addtitle><description>Increasing antimalarial drug resistance once again threatens effective antimalarial drug treatment, malaria control, and elimination. Artemisinin combination therapies (ACTs) are first-line treatment for uncomplicated falciparum malaria in all endemic countries, yet partial resistance to artemisinins has emerged in the Greater Mekong Subregion. Concomitant emergence of partner drug resistance is now causing high ACT treatment failure rates in several areas. Genetic markers for artemisinin resistance and several of the partner drugs have been established, greatly facilitating surveillance. Single point mutations in the gene coding for the Kelch propeller domain of the K13 protein strongly correlate with artemisinin resistance. Novel regimens and strategies using existing antimalarial drugs will be needed until novel compounds can be deployed. Elimination of artemisinin resistance will imply elimination of all falciparum malaria from the same areas. In vivax malaria, chloroquine resistance is an increasing problem.</description><subject>Antigens, Bacterial</subject><subject>Antigens, Bacterial - genetics</subject><subject>Antigens, Surface</subject><subject>Antigens, Surface - genetics</subject><subject>Antimalarials</subject><subject>Antimalarials - pharmacology</subject><subject>Artemisinins</subject><subject>Artemisinins - pharmacology</subject><subject>Drug Resistance</subject><subject>Drug Resistance - genetics</subject><subject>Drug Therapy, Combination</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Life Sciences</subject><subject>Malaria, Falciparum</subject><subject>Malaria, Falciparum - drug therapy</subject><subject>Malaria, Vivax</subject><subject>Malaria, Vivax - drug therapy</subject><subject>Plasmodium</subject><subject>Plasmodium - drug effects</subject><subject>Plasmodium - genetics</subject><issn>2157-1422</issn><issn>2472-5412</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpdUVFLwzAQDqK4MfcLBOmjPnQmadI0gkKZ0wkTQeZzSNN0i3TtTNKB_96MzTG9lxx33_fdXT4ALhEcIQTRrXLLtbZurZUfSYhpivgJ6GPCcEwJwqchR5TFiGDcA0PnPmEImqYZg-eghzOccUyyPrjPG29WspbWyDp6tN0ietfOOC8bpe-iPJovrZY-8m30ukNFk9qsTCO9aZsLcFbJ2unh_h2Aj6fJfDyNZ2_PL-N8FiuScB8zzgta8RIznCmiaVpkNFGyULAiLKnCPbxEVGGiSyQJTXlW0oqoQhYFoVzJZAAedrrrrljpUunGW1mLtQ2r22_RSiP-dhqzFIt2IyjhFNIkCNzsBJb_aNN8Jra18IWUJ5BvUMBe74fZ9qvTzouVcUrXtWx02zmBMsYoTjlKAzTZQZVtnbO6OmgjKLY-iSOfxN6nwLo6vubA-XUl-QEFypG0</recordid><startdate>20170701</startdate><enddate>20170701</enddate><creator>Menard, Didier</creator><creator>Dondorp, Arjen</creator><general>Cold Spring Harbor Laboratory Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1357-4495</orcidid></search><sort><creationdate>20170701</creationdate><title>Antimalarial Drug Resistance: A Threat to Malaria Elimination</title><author>Menard, Didier ; Dondorp, Arjen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-799b5f9d2728c4e56b853cabc0f473f1019d15c24ed1a45698d5f4cbabb459ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antigens, Bacterial</topic><topic>Antigens, Bacterial - genetics</topic><topic>Antigens, Surface</topic><topic>Antigens, Surface - genetics</topic><topic>Antimalarials</topic><topic>Antimalarials - pharmacology</topic><topic>Artemisinins</topic><topic>Artemisinins - pharmacology</topic><topic>Drug Resistance</topic><topic>Drug Resistance - genetics</topic><topic>Drug Therapy, Combination</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Life Sciences</topic><topic>Malaria, Falciparum</topic><topic>Malaria, Falciparum - drug therapy</topic><topic>Malaria, Vivax</topic><topic>Malaria, Vivax - drug therapy</topic><topic>Plasmodium</topic><topic>Plasmodium - drug effects</topic><topic>Plasmodium - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Menard, Didier</creatorcontrib><creatorcontrib>Dondorp, Arjen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cold Spring Harbor perspectives in medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Menard, Didier</au><au>Dondorp, Arjen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antimalarial Drug Resistance: A Threat to Malaria Elimination</atitle><jtitle>Cold Spring Harbor perspectives in medicine</jtitle><addtitle>Cold Spring Harb Perspect Med</addtitle><date>2017-07-01</date><risdate>2017</risdate><volume>7</volume><issue>7</issue><spage>a025619</spage><pages>a025619-</pages><issn>2157-1422</issn><eissn>2472-5412</eissn><abstract>Increasing antimalarial drug resistance once again threatens effective antimalarial drug treatment, malaria control, and elimination. Artemisinin combination therapies (ACTs) are first-line treatment for uncomplicated falciparum malaria in all endemic countries, yet partial resistance to artemisinins has emerged in the Greater Mekong Subregion. Concomitant emergence of partner drug resistance is now causing high ACT treatment failure rates in several areas. Genetic markers for artemisinin resistance and several of the partner drugs have been established, greatly facilitating surveillance. Single point mutations in the gene coding for the Kelch propeller domain of the K13 protein strongly correlate with artemisinin resistance. Novel regimens and strategies using existing antimalarial drugs will be needed until novel compounds can be deployed. Elimination of artemisinin resistance will imply elimination of all falciparum malaria from the same areas. In vivax malaria, chloroquine resistance is an increasing problem.</abstract><cop>United States</cop><pub>Cold Spring Harbor Laboratory Press</pub><pmid>28289248</pmid><doi>10.1101/cshperspect.a025619</doi><orcidid>https://orcid.org/0000-0003-1357-4495</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2157-1422 |
ispartof | Cold Spring Harbor perspectives in medicine, 2017-07, Vol.7 (7), p.a025619 |
issn | 2157-1422 2472-5412 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5495053 |
source | PubMed Central |
subjects | Antigens, Bacterial Antigens, Bacterial - genetics Antigens, Surface Antigens, Surface - genetics Antimalarials Antimalarials - pharmacology Artemisinins Artemisinins - pharmacology Drug Resistance Drug Resistance - genetics Drug Therapy, Combination Human health and pathology Humans Infectious diseases Life Sciences Malaria, Falciparum Malaria, Falciparum - drug therapy Malaria, Vivax Malaria, Vivax - drug therapy Plasmodium Plasmodium - drug effects Plasmodium - genetics |
title | Antimalarial Drug Resistance: A Threat to Malaria Elimination |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T02%3A42%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Antimalarial%20Drug%20Resistance:%20A%20Threat%20to%20Malaria%20Elimination&rft.jtitle=Cold%20Spring%20Harbor%20perspectives%20in%20medicine&rft.au=Menard,%20Didier&rft.date=2017-07-01&rft.volume=7&rft.issue=7&rft.spage=a025619&rft.pages=a025619-&rft.issn=2157-1422&rft.eissn=2472-5412&rft_id=info:doi/10.1101/cshperspect.a025619&rft_dat=%3Cproquest_pubme%3E1877526916%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c439t-799b5f9d2728c4e56b853cabc0f473f1019d15c24ed1a45698d5f4cbabb459ca3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1877526916&rft_id=info:pmid/28289248&rfr_iscdi=true |