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      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="bold" font="default" size="100%">Guemouri, Sayeh</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Dégbègni, R.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Courtois, L.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Accrombessi, M.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Massougbodji, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ding, X. C.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Tuikue Ndam, Nicaise</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Mama, A.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Fievet, Nadine</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Sarrasin-Hubert, V.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Cotrell, G.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Briand, Valérie</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Dynamics of persistent submicroscopic and microscopic Plasmodium falciparum in pregnant women under intermittent preventive treatment : a study cohort in Benin</title>
        <secondary-title>Open Forum Infectious Diseases</secondary-title>
      </titles>
      <pages>ofae762 [9 p.]</pages>
      <keywords>
        <keyword>intermittent preventive treatment</keyword>
        <keyword>msp-2 fragment analysis method</keyword>
        <keyword>plasmodium falciparum</keyword>
        <keyword>pregnancy</keyword>
        <keyword>submicroscopic</keyword>
        <keyword>BENIN</keyword>
        <keyword>AFRIQUE SUBSAHARIENNE</keyword>
      </keywords>
      <dates>
        <year>2025</year>
      </dates>
      <call-num>fdi:010092616</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Open Forum Infectious Diseases</full-title>
      </periodical>
      <isbn>2328-8957</isbn>
      <accession-num>ISI:001399230300001</accession-num>
      <number>1</number>
      <electronic-resource-num>10.1093/ofid/ofae762</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010092616</url>
        </related-urls>
        <pdf-urls>
          <url>https://horizon.documentation.ird.fr/exl-doc/pleins_textes/2025-02/010092616.pdf</url>
        </pdf-urls>
      </urls>
      <volume>12</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Background Malaria infections in pregnancy are a major cause of maternal morbidity and neonatal mortality in sub-Saharan Africa. A high proportion of these infections are submicroscopic, which are usually asymptomatic and therefore untreated during pregnancy. Intermittent preventive treatment with sulfadoxine-pyrimethamine (IPTp-SP) aims to prevent and treat all potential infections whether submicroscopic or not. However, the resistance of parasites to SP is steadily increasing. The dynamic of microscopic and submicroscopic infections in a cohort of Beninese women throughout their pregnancy and its relation to IPTp-SP has been assessed.Methods As a subsample of the RECIPAL project, 130 women with at least 2 infections detected by polymerase chain reaction during their pregnancy were included. Infections were categorized as new (isolated) or persistent based on msp-2 genotyping, where persistent infections had identical genotypes in all studied time points. Submicroscopic infections were defined as polymerase chain reaction-positive and thick blood smear-negative. The persistence of infections according to IPTp-SP uptake was assessed.Results A total of 73.1% of women (95 women of 130) had exclusively persistent infections throughout their pregnancy, whereas only 7.7% (10 of 130) had exclusively new infections. During pregnancy, the median time spent with 1 persistent infection was 7.2 weeks. A considerable proportion of these persistent infections 64.3% (72 of 113) was only submicroscopic. Approximately 20% of these persistent infections occurred despite the use of IPTp-SP.Conclusions Using new antimalarial combinations could contribute to limit the persistence of submicroscopic infections and their probable negative effects on the mother and the fetus. Intermittent preventive treatment with sulfadoxine-pyrimethamine prevents malaria in pregnant women in Africa. A sensitive genotyping method shows that a considerable number of women have persistent infections throughout pregnancy despite this treatment. Using new antimalarial combinations could contribute to limit this persistence.</abstract>
      <custom6>050 ; 052</custom6>
      <custom1>UR261</custom1>
      <custom7>Bénin</custom7>
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