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      <title>Evolution of renal function in African patients initiating second-line antiretroviral treatment : findings from the ANRS 12169 2LADY trial</title>
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    <abstract>Background: To investigate change in renal function in African patients initiating second-line antiretroviral therapy (ART) including ritonavir-boosted protease inhibitor (PI/r) with or without tenofovir disoproxil fumarate (TDF). Methods: HIV-1-positive adults, failing standard first-line ART were randomized to either TDF/emtricitabine (FTC)+LPV/r, abacavir + didanosine +LPV/r or TDF/FTC+darunavir (DRV)/r and followed for 18 months. Patients with an estimated glomerular filtration rate (eGFR) &gt;= 60 ml/min/1.73 m(2) at baseline were included in this analysis. Results: Data from 438 out of 454 randomized patients were analysed. Median age was 38 years and 72% were women. Initiation of PI/r-based second-line regimen induced a marked eGFR decline of -10.5 ml/min/1.73 m2 at week 4 in all treatment groups with a greater decrease in TDF/FTC+LPV/r arm (-15.1 ml/min/1.73 m(2)). At month 18, mean eGFR in the non-TDF containing regimen recovered its baseline level and was significantly greater than eGFR 18-month levels in the TDF-containing regimens that experienced only partial recovery (difference: -10.7; CI -16.8, -4.6; P=0.001 in TDF/FTC+LPV/r and -6.4; CI -12.5, -0.3; P=0.04 in TDF/FTC+DRV/r). At 18 months, prevalence of stage 3 chronic kidney disease was low (&lt;3%) and not associated with treatment. One treatment discontinuation and five TDF dosage reductions for renal toxicities were reported in TDF-containing arms. Conclusions: Overall, these results suggest a reasonable renal tolerance of a regimen associating TDF/FTC+ PI/r in African patients with eGFR&gt;60 ml/ml/1.73 m(2) at baseline. They also support the recommendation of reassessing renal function 1 month after initiation of treatment including ritonavir to account for the ritonavir-related artefactual decrease of eGFR and determine the new reference baseline value.</abstract>
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      <geographic>CAMEROUN</geographic>
      <geographic>BURKINA FASO</geographic>
      <geographic>SENEGAL</geographic>
      <geographic>YAOUNDE</geographic>
      <geographic>BOBO DIOULASSO</geographic>
      <geographic>DAKAR</geographic>
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    <classification authority="local">050</classification>
    <classification authority="local">052</classification>
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      <titleInfo>
        <title>Antiviral Therapy</title>
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      <part>
        <detail type="volume">
          <number>22</number>
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        <detail type="volume">
          <number>3</number>
        </detail>
        <extent unit="pages">
          <list> 195-203</list>
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      <originInfo>
        <dateIssued>2017</dateIssued>
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      <identifier type="issn">1359-6535</identifier>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010072038</identifier>
    <identifier type="doi">10.3851/imp3097</identifier>
    <identifier type="issn">1359-6535</identifier>
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      <recordCreationDate encoding="w3cdtf">2018-03-05</recordCreationDate>
      <recordChangeDate encoding="w3cdtf">2023-07-11</recordChangeDate>
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