Image from Google Jackets

Factors influencing efavirenz and nevirapine plasma concentration: effect of ethnicity, weight and co-medication.

By: Contributor(s): Publication details: 2008ISSN:
  • 13596535
Uniform titles:
  • Antiviral therapy.
Online resources: Summary: <div><h4>BACKGROUND: </h4><p>The aim of this study was to examine <span class="highlight" style="background-color:">factors</span> <span class="highlight" style="background-color:">influencing</span> <span class="highlight" style="background-color:">plasma</span> <span class="highlight" style="background-color:">concentration</span> of <span class="highlight" style="background-color:">efavirenz</span> and <span class="highlight" style="background-color:">nevirapine</span>.</p><h4>METHODS: </h4><p>Data from the Liverpool Therapeutic Drug Monitoring (TDM) registry were linked with the UK Collaborative HIV Cohort (CHIC) Study. For each patient, the first measurement of <span class="highlight" style="background-color:">efavirenz</span> (600 or 800 mg/day) or <span class="highlight" style="background-color:">nevirapine</span> (400 mg/day) <span class="highlight" style="background-color:">plasma</span> <span class="highlight" style="background-color:">concentration</span> was included. Linear regression was used to evaluate the association of dose, gender, age, <span class="highlight" style="background-color:">weight</span>, <span class="highlight" style="background-color:">ethnicity</span> and concomitant antiretroviral drugs or rifampicin with log-transformed drug <span class="highlight" style="background-color:">concentration</span>, adjusted for time since last intake.</p><h4>RESULTS: </h4><p>Data from 339 patients on <span class="highlight" style="background-color:">efavirenz</span> (34% black, 17% rifampicin) and 179 on <span class="highlight" style="background-color:">nevirapine</span> (27% black, 6% rifampicin) were included. Multivariable models revealed the following predictors for <span class="highlight" style="background-color:">efavirenz</span> <span class="highlight" style="background-color:">concentration</span>: black <span class="highlight" style="background-color:">ethnicity</span> (59% higher; P<0.001), <span class="highlight" style="background-color:">weight</span> (10% lower per additional 10 kg; P=0.002), 800 mg/day (52% higher; P=0.027), rifampicin (35% lower; P=0.039), and zidovudine (25% lower; P=0.010). Notably, without adjustment for other <span class="highlight" style="background-color:">factors</span>, patients on rifampicin had 48% higher <span class="highlight" style="background-color:">efavirenz</span> <span class="highlight" style="background-color:">concentration</span>, as these patients were mostly black and on 800 mg/day. For <span class="highlight" style="background-color:">nevirapine</span> the predictors were black <span class="highlight" style="background-color:">ethnicity</span> (39% higher; P=0.002), rifampicin (40% lower; P=0.002), protease inhibitor (28% higher; P=0.008) and tenofovir (22% higher; P=0.024).</p><h4>CONCLUSIONS: </h4><p>We observed clear associations between <span class="highlight" style="background-color:">ethnicity</span> and concentrations of <span class="highlight" style="background-color:">nevirapine</span> and <span class="highlight" style="background-color:">efavirenz</span>. Our analyses confirm that concomitant rifampicin substantially decreases <span class="highlight" style="background-color:">concentration</span> of both <span class="highlight" style="background-color:">efavirenz</span> and <span class="highlight" style="background-color:">nevirapine</span>; however, for <span class="highlight" style="background-color:">efavirenz</span> this <span class="highlight" style="background-color:">effect</span> was more than counterbalanced by the <span class="highlight" style="background-color:">effect</span> of <span class="highlight" style="background-color:">ethnicity</span> and increased <span class="highlight" style="background-color:">efavirenz</span> dose. There was also an additional impact of <span class="highlight" style="background-color:">weight</span>, which should be considered when determining optimal dosage. Other associations from our analysis (between tenofovir or protease inhibitor and <span class="highlight" style="background-color:">nevirapine</span>, and zidovudine and <span class="highlight" style="background-color:">efavirenz</span>), require confirmation in formal pharmacokinetic studies.</p></div>
Star ratings
    Average rating: 0.0 (0 votes)
Holdings
Item type Home library Collection Class number Status Date due Barcode
Book Ferriman information and Library Service (North Middlesex) Shelves Staff publications for NMDX Available

NMUH Staff Publications

13

&lt;div&gt;&lt;h4&gt;BACKGROUND: &lt;/h4&gt;&lt;p&gt;The aim of this study was to examine &lt;span class="highlight" style="background-color:"&gt;factors&lt;/span&gt; &lt;span class="highlight" style="background-color:"&gt;influencing&lt;/span&gt; &lt;span class="highlight" style="background-color:"&gt;plasma&lt;/span&gt; &lt;span class="highlight" style="background-color:"&gt;concentration&lt;/span&gt; of &lt;span class="highlight" style="background-color:"&gt;efavirenz&lt;/span&gt; and &lt;span class="highlight" style="background-color:"&gt;nevirapine&lt;/span&gt;.&lt;/p&gt;&lt;h4&gt;METHODS: &lt;/h4&gt;&lt;p&gt;Data from the Liverpool Therapeutic Drug Monitoring (TDM) registry were linked with the UK Collaborative HIV Cohort (CHIC) Study. For each patient, the first measurement of &lt;span class="highlight" style="background-color:"&gt;efavirenz&lt;/span&gt; (600 or 800 mg/day) or &lt;span class="highlight" style="background-color:"&gt;nevirapine&lt;/span&gt; (400 mg/day) &lt;span class="highlight" style="background-color:"&gt;plasma&lt;/span&gt; &lt;span class="highlight" style="background-color:"&gt;concentration&lt;/span&gt; was included. Linear regression was used to evaluate the association of dose, gender, age, &lt;span class="highlight" style="background-color:"&gt;weight&lt;/span&gt;, &lt;span class="highlight" style="background-color:"&gt;ethnicity&lt;/span&gt; and concomitant antiretroviral drugs or rifampicin with log-transformed drug &lt;span class="highlight" style="background-color:"&gt;concentration&lt;/span&gt;, adjusted for time since last intake.&lt;/p&gt;&lt;h4&gt;RESULTS: &lt;/h4&gt;&lt;p&gt;Data from 339 patients on &lt;span class="highlight" style="background-color:"&gt;efavirenz&lt;/span&gt; (34% black, 17% rifampicin) and 179 on &lt;span class="highlight" style="background-color:"&gt;nevirapine&lt;/span&gt; (27% black, 6% rifampicin) were included. Multivariable models revealed the following predictors for &lt;span class="highlight" style="background-color:"&gt;efavirenz&lt;/span&gt; &lt;span class="highlight" style="background-color:"&gt;concentration&lt;/span&gt;: black &lt;span class="highlight" style="background-color:"&gt;ethnicity&lt;/span&gt; (59% higher; P&amp;lt;0.001), &lt;span class="highlight" style="background-color:"&gt;weight&lt;/span&gt; (10% lower per additional 10 kg; P=0.002), 800 mg/day (52% higher; P=0.027), rifampicin (35% lower; P=0.039), and zidovudine (25% lower; P=0.010). Notably, without adjustment for other &lt;span class="highlight" style="background-color:"&gt;factors&lt;/span&gt;, patients on rifampicin had 48% higher &lt;span class="highlight" style="background-color:"&gt;efavirenz&lt;/span&gt; &lt;span class="highlight" style="background-color:"&gt;concentration&lt;/span&gt;, as these patients were mostly black and on 800 mg/day. For &lt;span class="highlight" style="background-color:"&gt;nevirapine&lt;/span&gt; the predictors were black &lt;span class="highlight" style="background-color:"&gt;ethnicity&lt;/span&gt; (39% higher; P=0.002), rifampicin (40% lower; P=0.002), protease inhibitor (28% higher; P=0.008) and tenofovir (22% higher; P=0.024).&lt;/p&gt;&lt;h4&gt;CONCLUSIONS: &lt;/h4&gt;&lt;p&gt;We observed clear associations between &lt;span class="highlight" style="background-color:"&gt;ethnicity&lt;/span&gt; and concentrations of &lt;span class="highlight" style="background-color:"&gt;nevirapine&lt;/span&gt; and &lt;span class="highlight" style="background-color:"&gt;efavirenz&lt;/span&gt;. Our analyses confirm that concomitant rifampicin substantially decreases &lt;span class="highlight" style="background-color:"&gt;concentration&lt;/span&gt; of both &lt;span class="highlight" style="background-color:"&gt;efavirenz&lt;/span&gt; and &lt;span class="highlight" style="background-color:"&gt;nevirapine&lt;/span&gt;; however, for &lt;span class="highlight" style="background-color:"&gt;efavirenz&lt;/span&gt; this &lt;span class="highlight" style="background-color:"&gt;effect&lt;/span&gt; was more than counterbalanced by the &lt;span class="highlight" style="background-color:"&gt;effect&lt;/span&gt; of &lt;span class="highlight" style="background-color:"&gt;ethnicity&lt;/span&gt; and increased &lt;span class="highlight" style="background-color:"&gt;efavirenz&lt;/span&gt; dose. There was also an additional impact of &lt;span class="highlight" style="background-color:"&gt;weight&lt;/span&gt;, which should be considered when determining optimal dosage. Other associations from our analysis (between tenofovir or protease inhibitor and &lt;span class="highlight" style="background-color:"&gt;nevirapine&lt;/span&gt;, and zidovudine and &lt;span class="highlight" style="background-color:"&gt;efavirenz&lt;/span&gt;), require confirmation in formal pharmacokinetic studies.&lt;/p&gt;&lt;/div&gt;

There are no comments on this title.

to post a comment.
London Health Libraries Koha Consortium privacy notice