<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>30(7)</volume><submitter>Colhoun HM</submitter><funding>Novo Nordisk A/S</funding><pubmed_abstract>The SELECT trial previously reported a 20% reduction in major adverse cardiovascular events with semaglutide (n = 8,803) versus placebo (n = 8,801) in patients with overweight/obesity and established cardiovascular disease, without diabetes. In the present study, we examined the effect of once-weekly semaglutide 2.4 mg on kidney outcomes in the SELECT trial. The incidence of the pre-specified main composite kidney endpoint (death from kidney disease, initiation of chronic kidney replacement therapy, onset of persistent estimated glomerular filtration rate (eGFR) &lt; 15 ml min&lt;sup>-1&lt;/sup> 1.73 m&lt;sup>-&lt;/sup>&lt;sup>2&lt;/sup>, persistent ≥50% reduction in eGFR or onset of persistent macroalbuminuria) was lower with semaglutide (1.8%) versus placebo (2.2%): hazard ratio (HR) = 0.78; 95% confidence i</pubmed_abstract><journal>Nature medicine</journal><pagination>2058-2066</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11271413</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Long-term kidney outcomes of semaglutide in obesity and cardiovascular disease in the SELECT trial.</pubmed_title><pmcid>PMC11271413</pmcid><pubmed_authors>Plutzky J</pubmed_authors><pubmed_authors>Deanfield J</pubmed_authors><pubmed_authors>Lingvay I</pubmed_authors><pubmed_authors>Node K</pubmed_authors><pubmed_authors>Rathor N</pubmed_authors><pubmed_authors>Tuttle KR</pubmed_authors><pubmed_authors>Lincoff AM</pubmed_authors><pubmed_authors>Wilding JPH</pubmed_authors><pubmed_authors>Brown-Frandsen K</pubmed_authors><pubmed_authors>Kahn SE</pubmed_authors><pubmed_authors>Mann JFE</pubmed_authors><pubmed_authors>Parkhomenko A</pubmed_authors><pubmed_authors>Ryden L</pubmed_authors><pubmed_authors>Idorn T</pubmed_authors><pubmed_authors>Brown PM</pubmed_authors><pubmed_authors>Colhoun HM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Long-term kidney outcomes of semaglutide in obesity and cardiovascular disease in the SELECT trial.</name><description>The SELECT trial previously reported a 20% reduction in major adverse cardiovascular events with semaglutide (n = 8,803) versus placebo (n = 8,801) in patients with overweight/obesity and established cardiovascular disease, without diabetes. In the present study, we examined the effect of once-weekly semaglutide 2.4 mg on kidney outcomes in the SELECT trial. The incidence of the pre-specified main composite kidney endpoint (death from kidney disease, initiation of chronic kidney replacement therapy, onset of persistent estimated glomerular filtration rate (eGFR) &lt; 15 ml min&lt;sup>-1&lt;/sup> 1.73 m&lt;sup>-&lt;/sup>&lt;sup>2&lt;/sup>, persistent ≥50% reduction in eGFR or onset of persistent macroalbuminuria) was lower with semaglutide (1.8%) versus placebo (2.2%): hazard ratio (HR) = 0.78; 95% confidence i</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-06-01T06:55:37.2Z</modification><creation>2025-04-19T13:11:38.367Z</creation></dates><accession>S-EPMC11271413</accession><cross_references><pubmed>38796653</pubmed><doi>10.1038/s41591-024-03015-5</doi></cross_references></HashMap>