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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%">Cournil, Amandine</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Hema, A.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Eymard-Duvernay, Sabrina</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ciaffi, L.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Badiou, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Kabore, F. N.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Diouf, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ayangma, L.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Le Moing, V.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Reynes, J.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Koulla-Shiro, S.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Delaporte, Eric</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Lady Study Grp</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Evolution of renal function in African patients initiating second-line antiretroviral treatment : findings from the ANRS 12169 2LADY trial</title>
        <secondary-title>Antiviral Therapy</secondary-title>
      </titles>
      <pages>195-203</pages>
      <keywords>
        <keyword>CAMEROUN</keyword>
        <keyword>BURKINA FASO</keyword>
        <keyword>SENEGAL</keyword>
        <keyword>YAOUNDE</keyword>
        <keyword>BOBO DIOULASSO</keyword>
        <keyword>DAKAR</keyword>
      </keywords>
      <dates>
        <year>2017</year>
      </dates>
      <call-num>fdi:010072038</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Antiviral Therapy</full-title>
      </periodical>
      <isbn>1359-6535</isbn>
      <accession-num>ISI:000423269400002</accession-num>
      <number>3</number>
      <electronic-resource-num>10.3851/imp3097</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010072038</url>
        </related-urls>
        <pdf-urls>
          <url>https://www.documentation.ird.fr/intranet/publi/2018/02/010072038.pdf</url>
        </pdf-urls>
      </urls>
      <volume>22</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <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>
      <custom6>050 ; 052</custom6>
      <custom1>UR233</custom1>
      <custom7>Burkina Faso / Cameroun / Sénégal</custom7>
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