<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hays AG</submitter><funding>NCATS NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIH HHS</funding><pagination>1041-1050</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8916096</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>35(7)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>People living with HIV (PWH) experience an increased burden of coronary artery disease (CAD) believed to be related, in part, to an interplay of chronically increased inflammation and traditional risk factors. Recent trials suggest cardiovascular benefits of the anti-inflammatory, colchicine, in HIV-seronegative CAD patients. However, the impact of colchicine on impaired vascular health, as measured by coronary endothelial function (CEF), an independent contributor to CAD, has not been studied in PWH. We tested the hypothesis that colchicine improves vascular health in PWH.&lt;h4>Design&lt;/h4>This was a randomized, placebo-controlled, double-blinded trial in 81 PWH to test whether low-dose colchicine (0.6 mg daily) improves CEF over 8-24 weeks.&lt;h4>Methods&lt;/h4>Coronary and sys</pubmed_abstract><journal>AIDS (London, England)</journal><pubmed_title>A randomized, placebo-controlled, double-blinded clinical trial of colchicine to improve vascular health in people living with HIV.</pubmed_title><pmcid>PMC8916096</pmcid><funding_grant_id>P30 CA006973</funding_grant_id><funding_grant_id>R56 HL125059</funding_grant_id><funding_grant_id>UL1 TR003098</funding_grant_id><funding_grant_id>U01 HL146201</funding_grant_id><funding_grant_id>K23 HL133358</funding_grant_id><funding_grant_id>R01 HL147660</funding_grant_id><funding_grant_id>S10 OD020091</funding_grant_id><funding_grant_id>R01 HL125059</funding_grant_id><funding_grant_id>P30 AI094189</funding_grant_id><pubmed_authors>Kelly S</pubmed_authors><pubmed_authors>Afework Y</pubmed_authors><pubmed_authors>Stradley S</pubmed_authors><pubmed_authors>Margolick JB</pubmed_authors><pubmed_authors>Barditch-Crovo P</pubmed_authors><pubmed_authors>Meyer J</pubmed_authors><pubmed_authors>Schar M</pubmed_authors><pubmed_authors>Bonanno G</pubmed_authors><pubmed_authors>Weiss RG</pubmed_authors><pubmed_authors>Anders NM</pubmed_authors><pubmed_authors>Hays AG</pubmed_authors><pubmed_authors>Lai S</pubmed_authors><pubmed_authors>Streeb V</pubmed_authors><pubmed_authors>Gerstenblith G</pubmed_authors><pubmed_authors>Bagchi S</pubmed_authors></additional><is_claimable>false</is_claimable><name>A randomized, placebo-controlled, double-blinded clinical trial of colchicine to improve vascular health in people living with HIV.</name><description>&lt;h4>Objectives&lt;/h4>People living with HIV (PWH) experience an increased burden of coronary artery disease (CAD) believed to be related, in part, to an interplay of chronically increased inflammation and traditional risk factors. Recent trials suggest cardiovascular benefits of the anti-inflammatory, colchicine, in HIV-seronegative CAD patients. However, the impact of colchicine on impaired vascular health, as measured by coronary endothelial function (CEF), an independent contributor to CAD, has not been studied in PWH. We tested the hypothesis that colchicine improves vascular health in PWH.&lt;h4>Design&lt;/h4>This was a randomized, placebo-controlled, double-blinded trial in 81 PWH to test whether low-dose colchicine (0.6 mg daily) improves CEF over 8-24 weeks.&lt;h4>Methods&lt;/h4>Coronary and sys</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jun</publication><modification>2026-05-09T20:14:03.152Z</modification><creation>2025-04-04T22:01:52.403Z</creation></dates><accession>S-EPMC8916096</accession><cross_references><pubmed>33587443</pubmed><doi>10.1097/QAD.0000000000002845</doi><doi>10.1097/qad.0000000000002845</doi></cross_references></HashMap>