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    <titleInfo>
      <title>Influence of CYP2B6 polymorphisms on the persistence of plasma nevirapine concentrations following a single intra-partum dose for the prevention of mother to child transmission in HIV-infected Thai women</title>
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      <namePart type="family">Chantarangsu</namePart>
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      <namePart type="family">Ngo Giang Huong</namePart>
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    <abstract>To investigate the association of single nucleotide polymorphisms (SNPs) with nevirapine concentrations following intra-partum single-dose nevirapine. Plasma and DNA samples were obtained from 330 HIV-infected Thai women who received intra-partum single-dose nevirapine in the PHPT-2 clinical trial to prevent perinatal HIV transmission. Nine SNPs within CYP2B6, CYP3A4 and ABCB1 were genotyped by real-time PCR. Nevirapine plasma concentrations were determined by HPLC and used in a population pharmacokinetic analysis. Higher nevirapine exposure was observed in women carrying the CYP2B6 516G &gt; T polymorphism, but this did not reach statistical significance (P = 0.054). The TGATC CYP2B6 haplotype (g.3003T, 516G, 785A, g.18492T and g.21563C) was associated with increased nevirapine clearance and lower exposure (P = 0.0029). The median time for nevirapine concentrations to reach 10 ng/mL post-partum (nevirapine IC50 for HIV-1) was 14 days [interquartile range (IQR, 14-18)] for TGATC homozygotes, 16 days (14-20) for TGATC heterozygotes and 18 days (14-20) for non-TGATC homozygotes (P = 0.020). The CYP2B6 516G &gt; T impact on nevirapine concentrations was less pronounced after intra-partum single-dose nevirapine than reported under steady-state conditions, perhaps due to lack of enzyme auto-induction at the time of dosing. Although the TGATC CYP2B6 haplotype may shorten the persistence of nevirapine post-partum, its practical implications for the prevention of HIV transmission or selection of resistance mutations are likely limited.</abstract>
    <targetAudience authority="marctarget">specialized</targetAudience>
    <subject>
      <topic>pharmacogenetics</topic>
      <topic>single nucleotide polymorphisms</topic>
      <topic>SNPs</topic>
    </subject>
    <classification authority="local">052</classification>
    <relatedItem type="host">
      <titleInfo>
        <title>Journal of Antimicrobial Chemotherapy</title>
      </titleInfo>
      <part>
        <detail type="volume">
          <number>64</number>
        </detail>
        <detail type="volume">
          <number>6</number>
        </detail>
        <extent unit="pages">
          <list> 1265-1273</list>
        </extent>
      </part>
      <originInfo>
        <dateIssued>2009</dateIssued>
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      <identifier type="issn">0305-7453</identifier>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010052478</identifier>
    <identifier type="doi">10.1093/jac/dkp351</identifier>
    <identifier type="issn">0305-7453</identifier>
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      <url usage="primary display" access="object in context">https://www.documentation.ird.fr/hor/fdi:010052478</url>
      <url access="row object">https://www.documentation.ird.fr/intranet/publi/depot/2011-09-08/010052478.pdf</url>
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      <recordCreationDate encoding="w3cdtf">2009-12-21</recordCreationDate>
      <recordChangeDate encoding="w3cdtf">2017-08-23</recordChangeDate>
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