<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mayne KJ</submitter><funding>Clinical Trial Service Unit and Epidemiological Studies Unit</funding><funding>Medical Research Council</funding><pagination>720-730</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7616479</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>40(4)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Hyperuricaemia and gout are common in chronic kidney disease (CKD). We aimed to assess the effects of sodium-glucose co-transporter-2 (SGLT2) inhibition on uric acid (urate) and gout in patients with CKD.&lt;h4>Methods&lt;/h4>The EMPA-KIDNEY trial randomised 6609 patients with CKD to receive either empagliflozin 10 mg daily or matching placebo over a median of 2 years of follow-up. Serum uric acid was measured at randomisation then at 2 and 18 months of follow-up and the effects of empagliflozin were analysed using a pre-specified mixed model repeated measures approach. Participant-reported gout events were analysed in Cox regression models (first events) with the Andersen-Gill extension (total events). A post hoc composite outcome included new initiation of uric acid-lowering</pubmed_abstract><journal>Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association</journal><pubmed_title>Empagliflozin lowers serum uric acid in chronic kidney disease: exploratory analyses from the EMPA-KIDNEY trial.</pubmed_title><pmcid>PMC7616479</pmcid><funding_grant_id>MC_UU_00017/4</funding_grant_id><funding_grant_id>MC_UU_00017/3</funding_grant_id><pubmed_authors>Green JB</pubmed_authors><pubmed_authors>George J</pubmed_authors><pubmed_authors>Hooi L</pubmed_authors><pubmed_authors>Pontremoli R</pubmed_authors><pubmed_authors>Cheung AK</pubmed_authors><pubmed_authors>Ng SYA</pubmed_authors><pubmed_authors>Judge P</pubmed_authors><pubmed_authors>Haynes R</pubmed_authors><pubmed_authors>Kadowaki T</pubmed_authors><pubmed_authors>Nangaku M</pubmed_authors><pubmed_authors>Judge PK</pubmed_authors><pubmed_authors>Goto S</pubmed_authors><pubmed_authors>Deo R</pubmed_authors><pubmed_authors>Wanner C</pubmed_authors><pubmed_authors>Liu W</pubmed_authors><pubmed_authors>Sammons E</pubmed_authors><pubmed_authors>Herrington WG</pubmed_authors><pubmed_authors>Whelton P</pubmed_authors><pubmed_authors>Baigent C</pubmed_authors><pubmed_authors>EMPA-KIDNEY Collaborative Group</pubmed_authors><pubmed_authors>Rossello X</pubmed_authors><pubmed_authors>Sardell RJ</pubmed_authors><pubmed_authors>Landray MJ</pubmed_authors><pubmed_authors>Emberson J</pubmed_authors><pubmed_authors>Hauske SJ</pubmed_authors><pubmed_authors>Levin A</pubmed_authors><pubmed_authors>Bilous R</pubmed_authors><pubmed_authors>Hantel S</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Bennett D</pubmed_authors><pubmed_authors>Brueckmann M</pubmed_authors><pubmed_authors>Cherney D</pubmed_authors><pubmed_authors>Hopley M</pubmed_authors><pubmed_authors>von-Eynatten M</pubmed_authors><pubmed_authors>Mayne KJ</pubmed_authors><pubmed_authors>Zhu D</pubmed_authors><pubmed_authors>Tuttle KR</pubmed_authors><pubmed_authors>Maggioni AP</pubmed_authors><pubmed_authors>Preiss D</pubmed_authors><pubmed_authors>Wittes J</pubmed_authors><pubmed_authors>Sandercock P</pubmed_authors><pubmed_authors>Cherney DZI</pubmed_authors><pubmed_authors>Staplin N</pubmed_authors><pubmed_authors>Liu ZH</pubmed_authors><pubmed_authors>Herzog C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Empagliflozin lowers serum uric acid in chronic kidney disease: exploratory analyses from the EMPA-KIDNEY trial.</name><description>&lt;h4>Background&lt;/h4>Hyperuricaemia and gout are common in chronic kidney disease (CKD). We aimed to assess the effects of sodium-glucose co-transporter-2 (SGLT2) inhibition on uric acid (urate) and gout in patients with CKD.&lt;h4>Methods&lt;/h4>The EMPA-KIDNEY trial randomised 6609 patients with CKD to receive either empagliflozin 10 mg daily or matching placebo over a median of 2 years of follow-up. Serum uric acid was measured at randomisation then at 2 and 18 months of follow-up and the effects of empagliflozin were analysed using a pre-specified mixed model repeated measures approach. Participant-reported gout events were analysed in Cox regression models (first events) with the Andersen-Gill extension (total events). A post hoc composite outcome included new initiation of uric acid-lowering</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-06-03T05:18:10.106Z</modification><creation>2025-04-04T08:21:43.669Z</creation></dates><accession>S-EPMC7616479</accession><cross_references><pubmed>39277784</pubmed><doi>10.1093/ndt/gfae203</doi></cross_references></HashMap>