<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Coelho LE</submitter><funding>French National Agency</funding><funding>ANRS MIE</funding><funding>NIAID NIH HHS</funding><funding>Brazilian Ministry of Health</funding><funding>Merck Sharp Dohme-Chibret</funding><pagination>ofae035</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10939434</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>After antiretroviral therapy (ART) initiation, people with HIV (PWH) treated for tuberculosis (TB) may develop TB-associated immune reconstitution inflammatory syndrome (TB-IRIS). Integrase inhibitors, by providing a faster HIV-RNA decline than efavirenz, might increase the risk for this complication. We sought to assess incidence and determinants of TB-IRIS in PWH with TB on raltegravir- or efavirenz-based ART.&lt;h4>Methods&lt;/h4>We conducted a secondary analysis of the Reflate TB 2 trial, which randomized ART-naive PWH on standard TB treatment, to receive raltegravir- or efavirenz-based ART. The primary objective was to evaluate the incidence of TB-IRIS. Incidence rate ratio comparing TB-IRIS incidence in each arm was calculated. Kaplan-Meier curves were used to compare TB</pubmed_abstract><journal>Open forum infectious diseases</journal><pubmed_title>Incidence and Predictors of Tuberculosis-associated IRIS in People With HIV Treated for Tuberculosis: Findings From Reflate TB2 Randomized Trial.</pubmed_title><pmcid>PMC10939434</pmcid><funding_grant_id>ANRS 12300</funding_grant_id><funding_grant_id>UM1 AI069476</funding_grant_id><pubmed_authors>Laureillard D</pubmed_authors><pubmed_authors>Chau GD</pubmed_authors><pubmed_authors>Cardoso SW</pubmed_authors><pubmed_authors>Veloso VG</pubmed_authors><pubmed_authors>Coelho LE</pubmed_authors><pubmed_authors>Escada R</pubmed_authors><pubmed_authors>Eholie S</pubmed_authors><pubmed_authors>De Castro N</pubmed_authors><pubmed_authors>Molina JM</pubmed_authors><pubmed_authors>Messou E</pubmed_authors><pubmed_authors>Grinsztejn B</pubmed_authors><pubmed_authors>Marcy O</pubmed_authors><pubmed_authors>Chazallon C</pubmed_authors><pubmed_authors>Timana I</pubmed_authors><pubmed_authors>Khosa C</pubmed_authors><pubmed_authors>N'takpe JB</pubmed_authors><pubmed_authors>Delaugerre C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Incidence and Predictors of Tuberculosis-associated IRIS in People With HIV Treated for Tuberculosis: Findings From Reflate TB2 Randomized Trial.</name><description>&lt;h4>Background&lt;/h4>After antiretroviral therapy (ART) initiation, people with HIV (PWH) treated for tuberculosis (TB) may develop TB-associated immune reconstitution inflammatory syndrome (TB-IRIS). Integrase inhibitors, by providing a faster HIV-RNA decline than efavirenz, might increase the risk for this complication. We sought to assess incidence and determinants of TB-IRIS in PWH with TB on raltegravir- or efavirenz-based ART.&lt;h4>Methods&lt;/h4>We conducted a secondary analysis of the Reflate TB 2 trial, which randomized ART-naive PWH on standard TB treatment, to receive raltegravir- or efavirenz-based ART. The primary objective was to evaluate the incidence of TB-IRIS. Incidence rate ratio comparing TB-IRIS incidence in each arm was calculated. Kaplan-Meier curves were used to compare TB</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-07-16T04:16:18.653Z</modification><creation>2026-07-09T10:38:26.885Z</creation></dates><accession>S-EPMC10939434</accession><cross_references><pubmed>38486816</pubmed><doi>10.1093/ofid/ofae035</doi></cross_references></HashMap>