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High rates of parasite recrudescence following intermittent preventive treatment with sulphadoxine-pyrimethamine during pregnancy in Benin
Despite widespread parasite resistance to sulphadoxine-pyrimethamine (SP) its use for intermittent preventative treatment during pregnancy remains the policy in Benin and throughout most of sub-Saharan Africa. In a prospective study, 982 pregnant women were recruited in Benin and followed until deli...
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Published in: | Malaria journal 2013-06, Vol.12 (1), p.195-195, Article 195 |
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creator | Moussiliou, Azizath De Tove, Yolande Sissinto-Savi Doritchamou, Justin Luty, Adrian J F Massougbodji, Achille Alifrangis, Michael Deloron, Philippe Ndam, Nicaise Tuikue |
description | Despite widespread parasite resistance to sulphadoxine-pyrimethamine (SP) its use for intermittent preventative treatment during pregnancy remains the policy in Benin and throughout most of sub-Saharan Africa.
In a prospective study, 982 pregnant women were recruited in Benin and followed until delivery. The prevalence of point mutations in the pfdhfr and pfdhps genes associated with Plasmodium falciparum resistance to SP during consecutive antenatal visits was determined. Parasites clearance among women infected at SP intake was assessed by microscopy and PCR. Association between the persistence of parasites and malaria consequences, were investigated. Recurrent parasites were genotyped to identify recrudescences from re-infections.
The prevalence of pfdhfr/pfdhps quadruple mutants (triple pfdhfr + single pfdhps) was consistently above 80% while quintuple and sextuple mutants remained low. Importantly the higly mutated parasites apparently never included the two key mutations, pfdhfr 164 L or pfdhps 540E. Based on PCR results, SP failed to clear existing parasitaemia in half (48%) of the women who were infected at IPTp schedule. The frequency of recrudescence reached 76% after the second dose. Women with persistent parasitaemia had an increased prevalence of anaemia (P = 0.03).
The data presented here, highlight the inability of SP to ensure optimal antiplasmodial protection in late pregnancy, and invite urgent consideration of an alternative drug or strategy. |
doi_str_mv | 10.1186/1475-2875-12-195 |
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In a prospective study, 982 pregnant women were recruited in Benin and followed until delivery. The prevalence of point mutations in the pfdhfr and pfdhps genes associated with Plasmodium falciparum resistance to SP during consecutive antenatal visits was determined. Parasites clearance among women infected at SP intake was assessed by microscopy and PCR. Association between the persistence of parasites and malaria consequences, were investigated. Recurrent parasites were genotyped to identify recrudescences from re-infections.
The prevalence of pfdhfr/pfdhps quadruple mutants (triple pfdhfr + single pfdhps) was consistently above 80% while quintuple and sextuple mutants remained low. Importantly the higly mutated parasites apparently never included the two key mutations, pfdhfr 164 L or pfdhps 540E. Based on PCR results, SP failed to clear existing parasitaemia in half (48%) of the women who were infected at IPTp schedule. The frequency of recrudescence reached 76% after the second dose. Women with persistent parasitaemia had an increased prevalence of anaemia (P = 0.03).
The data presented here, highlight the inability of SP to ensure optimal antiplasmodial protection in late pregnancy, and invite urgent consideration of an alternative drug or strategy.</description><identifier>ISSN: 1475-2875</identifier><identifier>EISSN: 1475-2875</identifier><identifier>DOI: 10.1186/1475-2875-12-195</identifier><identifier>PMID: 23758883</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adolescent ; Adult ; Antimalarials - adverse effects ; Antimalarials - pharmacology ; Antimalarials - therapeutic use ; Benin - epidemiology ; Dihydropteroate Synthase - genetics ; Drug Combinations ; Drug therapy ; Female ; Gene mutations ; Genetic aspects ; Genomics ; Haplotypes ; Health aspects ; Humans ; Malaria ; Malaria, Falciparum - drug therapy ; Malaria, Falciparum - epidemiology ; Malaria, Falciparum - parasitology ; Malaria, Falciparum - prevention & control ; Mutation ; Parasitemia ; Parasites ; Plasmodium falciparum ; Plasmodium falciparum - drug effects ; Plasmodium falciparum - genetics ; Point Mutation - drug effects ; Polymorphism, Single Nucleotide ; Pregnancy ; Pregnancy Complications, Infectious - drug therapy ; Pregnancy Complications, Infectious - epidemiology ; Pregnancy Complications, Infectious - parasitology ; Pregnancy Complications, Infectious - prevention & control ; Pregnant women ; Prevalence ; Prospective Studies ; Protozoan Proteins - genetics ; Pyrimethamine - adverse effects ; Pyrimethamine - pharmacology ; Pyrimethamine - therapeutic use ; Recurrence ; Sulfadoxine - adverse effects ; Sulfadoxine - pharmacology ; Sulfadoxine - therapeutic use ; Tetrahydrofolate Dehydrogenase - genetics ; Womens health ; Young Adult</subject><ispartof>Malaria journal, 2013-06, Vol.12 (1), p.195-195, Article 195</ispartof><rights>COPYRIGHT 2013 BioMed Central Ltd.</rights><rights>2013 Moussiliou et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2013 Moussiliou et al.; licensee BioMed Central Ltd. 2013 Moussiliou et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b584t-538cacf7d53103d453bb655d9a5d63007b5e6d5517d6ef571c85f825055e84f43</citedby><cites>FETCH-LOGICAL-b584t-538cacf7d53103d453bb655d9a5d63007b5e6d5517d6ef571c85f825055e84f43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3686599/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1370781071?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23758883$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moussiliou, Azizath</creatorcontrib><creatorcontrib>De Tove, Yolande Sissinto-Savi</creatorcontrib><creatorcontrib>Doritchamou, Justin</creatorcontrib><creatorcontrib>Luty, Adrian J F</creatorcontrib><creatorcontrib>Massougbodji, Achille</creatorcontrib><creatorcontrib>Alifrangis, Michael</creatorcontrib><creatorcontrib>Deloron, Philippe</creatorcontrib><creatorcontrib>Ndam, Nicaise Tuikue</creatorcontrib><title>High rates of parasite recrudescence following intermittent preventive treatment with sulphadoxine-pyrimethamine during pregnancy in Benin</title><title>Malaria journal</title><addtitle>Malar J</addtitle><description>Despite widespread parasite resistance to sulphadoxine-pyrimethamine (SP) its use for intermittent preventative treatment during pregnancy remains the policy in Benin and throughout most of sub-Saharan Africa.
In a prospective study, 982 pregnant women were recruited in Benin and followed until delivery. The prevalence of point mutations in the pfdhfr and pfdhps genes associated with Plasmodium falciparum resistance to SP during consecutive antenatal visits was determined. Parasites clearance among women infected at SP intake was assessed by microscopy and PCR. Association between the persistence of parasites and malaria consequences, were investigated. Recurrent parasites were genotyped to identify recrudescences from re-infections.
The prevalence of pfdhfr/pfdhps quadruple mutants (triple pfdhfr + single pfdhps) was consistently above 80% while quintuple and sextuple mutants remained low. Importantly the higly mutated parasites apparently never included the two key mutations, pfdhfr 164 L or pfdhps 540E. Based on PCR results, SP failed to clear existing parasitaemia in half (48%) of the women who were infected at IPTp schedule. The frequency of recrudescence reached 76% after the second dose. Women with persistent parasitaemia had an increased prevalence of anaemia (P = 0.03).
The data presented here, highlight the inability of SP to ensure optimal antiplasmodial protection in late pregnancy, and invite urgent consideration of an alternative drug or strategy.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Antimalarials - adverse effects</subject><subject>Antimalarials - pharmacology</subject><subject>Antimalarials - therapeutic use</subject><subject>Benin - epidemiology</subject><subject>Dihydropteroate Synthase - genetics</subject><subject>Drug Combinations</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Gene mutations</subject><subject>Genetic aspects</subject><subject>Genomics</subject><subject>Haplotypes</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Malaria</subject><subject>Malaria, Falciparum - drug therapy</subject><subject>Malaria, Falciparum - epidemiology</subject><subject>Malaria, Falciparum - parasitology</subject><subject>Malaria, Falciparum - prevention & control</subject><subject>Mutation</subject><subject>Parasitemia</subject><subject>Parasites</subject><subject>Plasmodium falciparum</subject><subject>Plasmodium falciparum - drug effects</subject><subject>Plasmodium falciparum - genetics</subject><subject>Point Mutation - drug effects</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Infectious - drug therapy</subject><subject>Pregnancy Complications, Infectious - epidemiology</subject><subject>Pregnancy Complications, Infectious - parasitology</subject><subject>Pregnancy Complications, Infectious - prevention & control</subject><subject>Pregnant women</subject><subject>Prevalence</subject><subject>Prospective Studies</subject><subject>Protozoan Proteins - genetics</subject><subject>Pyrimethamine - adverse effects</subject><subject>Pyrimethamine - pharmacology</subject><subject>Pyrimethamine - therapeutic use</subject><subject>Recurrence</subject><subject>Sulfadoxine - adverse effects</subject><subject>Sulfadoxine - pharmacology</subject><subject>Sulfadoxine - therapeutic use</subject><subject>Tetrahydrofolate Dehydrogenase - genetics</subject><subject>Womens health</subject><subject>Young Adult</subject><issn>1475-2875</issn><issn>1475-2875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp1Ustu1DAUjRCIlsKeFbLEhk2KHcexs0FqRy1FqsQG1pZj38y4SuxgO1PmF_hqHE0ZOqjIkh_3nnN8X0XxluBzQkTzkdSclZXIG6lK0rJnxenB9PzR_aR4FeMdxoQLXr0sTirKmRCCnha_bux6g4JKEJHv0aSCijYBCqDDbCBqcBpQ74fB31u3RtYlCKNNCVxCU4BtPu0WUAqg0rgY723aoDgP00YZ_9M6KKddsCOkjRrzC5k5LEKZu3bK6V2WRJfgrHtdvOjVEOHNw3lWfL---ra6KW-_fv6yurgtOybqVDIqtNI9N4wSTE3NaNc1jJlWMdNQjHnHoDGMEW4a6BknWrBeVAwzBqLua3pWfNrrTnM3gskZpqAGOeUgVdhJr6w89ji7kWu_lbQRDWvbLLDaC3TW_0fg2KP9KJdeyKUXklQytyqrfHgII_gfM8QkR5vLPQzKgZ-jJLRtW8IwaTL0_T_QOz8Hl4uUURxzQTAnf1FrNYC0rvf5c72IygtG6yYXrl6CP38ClZeB0WrvoLfZfkTAe4IOPsYA_SFRguUyhU-l9u5xhQ-EP2NHfwO1jdsj</recordid><startdate>20130610</startdate><enddate>20130610</enddate><creator>Moussiliou, Azizath</creator><creator>De Tove, Yolande Sissinto-Savi</creator><creator>Doritchamou, Justin</creator><creator>Luty, Adrian J F</creator><creator>Massougbodji, Achille</creator><creator>Alifrangis, Michael</creator><creator>Deloron, Philippe</creator><creator>Ndam, Nicaise Tuikue</creator><general>BioMed Central Ltd</general><general>BioMed Central</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>3V.</scope><scope>7SS</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>K9.</scope><scope>L.G</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20130610</creationdate><title>High rates of parasite recrudescence following intermittent preventive treatment with sulphadoxine-pyrimethamine during pregnancy in Benin</title><author>Moussiliou, Azizath ; De Tove, Yolande Sissinto-Savi ; Doritchamou, Justin ; Luty, Adrian J F ; Massougbodji, Achille ; Alifrangis, Michael ; Deloron, Philippe ; Ndam, Nicaise Tuikue</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b584t-538cacf7d53103d453bb655d9a5d63007b5e6d5517d6ef571c85f825055e84f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Antimalarials - adverse effects</topic><topic>Antimalarials - pharmacology</topic><topic>Antimalarials - therapeutic use</topic><topic>Benin - epidemiology</topic><topic>Dihydropteroate Synthase - genetics</topic><topic>Drug Combinations</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Gene mutations</topic><topic>Genetic aspects</topic><topic>Genomics</topic><topic>Haplotypes</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Malaria</topic><topic>Malaria, Falciparum - drug therapy</topic><topic>Malaria, Falciparum - epidemiology</topic><topic>Malaria, Falciparum - parasitology</topic><topic>Malaria, Falciparum - prevention & control</topic><topic>Mutation</topic><topic>Parasitemia</topic><topic>Parasites</topic><topic>Plasmodium falciparum</topic><topic>Plasmodium falciparum - drug effects</topic><topic>Plasmodium falciparum - genetics</topic><topic>Point Mutation - drug effects</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Infectious - drug therapy</topic><topic>Pregnancy Complications, Infectious - epidemiology</topic><topic>Pregnancy Complications, Infectious - parasitology</topic><topic>Pregnancy Complications, Infectious - prevention & control</topic><topic>Pregnant women</topic><topic>Prevalence</topic><topic>Prospective Studies</topic><topic>Protozoan Proteins - genetics</topic><topic>Pyrimethamine - adverse effects</topic><topic>Pyrimethamine - pharmacology</topic><topic>Pyrimethamine - therapeutic use</topic><topic>Recurrence</topic><topic>Sulfadoxine - adverse effects</topic><topic>Sulfadoxine - pharmacology</topic><topic>Sulfadoxine - therapeutic use</topic><topic>Tetrahydrofolate Dehydrogenase - genetics</topic><topic>Womens health</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moussiliou, Azizath</creatorcontrib><creatorcontrib>De Tove, Yolande Sissinto-Savi</creatorcontrib><creatorcontrib>Doritchamou, Justin</creatorcontrib><creatorcontrib>Luty, Adrian J F</creatorcontrib><creatorcontrib>Massougbodji, Achille</creatorcontrib><creatorcontrib>Alifrangis, Michael</creatorcontrib><creatorcontrib>Deloron, Philippe</creatorcontrib><creatorcontrib>Ndam, Nicaise Tuikue</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database (Proquest)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Malaria journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moussiliou, Azizath</au><au>De Tove, Yolande Sissinto-Savi</au><au>Doritchamou, Justin</au><au>Luty, Adrian J F</au><au>Massougbodji, Achille</au><au>Alifrangis, Michael</au><au>Deloron, Philippe</au><au>Ndam, Nicaise Tuikue</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High rates of parasite recrudescence following intermittent preventive treatment with sulphadoxine-pyrimethamine during pregnancy in Benin</atitle><jtitle>Malaria journal</jtitle><addtitle>Malar J</addtitle><date>2013-06-10</date><risdate>2013</risdate><volume>12</volume><issue>1</issue><spage>195</spage><epage>195</epage><pages>195-195</pages><artnum>195</artnum><issn>1475-2875</issn><eissn>1475-2875</eissn><abstract>Despite widespread parasite resistance to sulphadoxine-pyrimethamine (SP) its use for intermittent preventative treatment during pregnancy remains the policy in Benin and throughout most of sub-Saharan Africa.
In a prospective study, 982 pregnant women were recruited in Benin and followed until delivery. The prevalence of point mutations in the pfdhfr and pfdhps genes associated with Plasmodium falciparum resistance to SP during consecutive antenatal visits was determined. Parasites clearance among women infected at SP intake was assessed by microscopy and PCR. Association between the persistence of parasites and malaria consequences, were investigated. Recurrent parasites were genotyped to identify recrudescences from re-infections.
The prevalence of pfdhfr/pfdhps quadruple mutants (triple pfdhfr + single pfdhps) was consistently above 80% while quintuple and sextuple mutants remained low. Importantly the higly mutated parasites apparently never included the two key mutations, pfdhfr 164 L or pfdhps 540E. Based on PCR results, SP failed to clear existing parasitaemia in half (48%) of the women who were infected at IPTp schedule. The frequency of recrudescence reached 76% after the second dose. Women with persistent parasitaemia had an increased prevalence of anaemia (P = 0.03).
The data presented here, highlight the inability of SP to ensure optimal antiplasmodial protection in late pregnancy, and invite urgent consideration of an alternative drug or strategy.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>23758883</pmid><doi>10.1186/1475-2875-12-195</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Antimalarials - adverse effects Antimalarials - pharmacology Antimalarials - therapeutic use Benin - epidemiology Dihydropteroate Synthase - genetics Drug Combinations Drug therapy Female Gene mutations Genetic aspects Genomics Haplotypes Health aspects Humans Malaria Malaria, Falciparum - drug therapy Malaria, Falciparum - epidemiology Malaria, Falciparum - parasitology Malaria, Falciparum - prevention & control Mutation Parasitemia Parasites Plasmodium falciparum Plasmodium falciparum - drug effects Plasmodium falciparum - genetics Point Mutation - drug effects Polymorphism, Single Nucleotide Pregnancy Pregnancy Complications, Infectious - drug therapy Pregnancy Complications, Infectious - epidemiology Pregnancy Complications, Infectious - parasitology Pregnancy Complications, Infectious - prevention & control Pregnant women Prevalence Prospective Studies Protozoan Proteins - genetics Pyrimethamine - adverse effects Pyrimethamine - pharmacology Pyrimethamine - therapeutic use Recurrence Sulfadoxine - adverse effects Sulfadoxine - pharmacology Sulfadoxine - therapeutic use Tetrahydrofolate Dehydrogenase - genetics Womens health Young Adult |
title | High rates of parasite recrudescence following intermittent preventive treatment with sulphadoxine-pyrimethamine during pregnancy in Benin |
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