<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(8)</volume><submitter>Liu H</submitter><funding>Merck &amp;amp; Co Inc</funding><funding>Pfizer Canada Inc</funding><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Sodium-glucose cotransporter-2 (SGLT2) inhibitors improve cardiovascular and kidney outcomes through mechanisms that are incompletely understood. In this exploratory post-hoc analysis of the VERTIS RENAL trial, we report the association between the SGLT2 inhibitor, ertugliflozin, and markers of kidney injury, inflammation, and fibrosis in participants with type 2 diabetes (T2D) and stage 3 chronic kidney disease (CKD).&lt;h4>Methods&lt;/h4>Participants were randomized to ertugliflozin (5 or 15 mg/d) or placebo, and plasma samples for biomarker analysis were collected at baseline, 26 weeks, and 52 weeks.&lt;h4>Results&lt;/h4>Ertugliflozin-treated participants had lower plasma levels of kidney injury molecule-1 (KIM-1) at 26 weeks (&lt;i>P&lt;/i> = 0.044) and 52 weeks (&lt;i>P&lt;/i> = 0.007) a</pubmed_abstract><journal>Kidney international reports</journal><pagination>2095-2104</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8343791</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Markers of Kidney Injury, Inflammation, and Fibrosis Associated With Ertugliflozin in Patients With CKD and Diabetes.</pubmed_title><pmcid>PMC8343791</pmcid><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Burger D</pubmed_authors><pubmed_authors>Burns K</pubmed_authors><pubmed_authors>Cherney DZI</pubmed_authors><pubmed_authors>Sridhar VS</pubmed_authors><pubmed_authors>Lytvyn Y</pubmed_authors><pubmed_authors>Brinc D</pubmed_authors><pubmed_authors>Lawler PR</pubmed_authors><pubmed_authors>Lovblom LE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Markers of Kidney Injury, Inflammation, and Fibrosis Associated With Ertugliflozin in Patients With CKD and Diabetes.</name><description>&lt;h4>Introduction&lt;/h4>Sodium-glucose cotransporter-2 (SGLT2) inhibitors improve cardiovascular and kidney outcomes through mechanisms that are incompletely understood. In this exploratory post-hoc analysis of the VERTIS RENAL trial, we report the association between the SGLT2 inhibitor, ertugliflozin, and markers of kidney injury, inflammation, and fibrosis in participants with type 2 diabetes (T2D) and stage 3 chronic kidney disease (CKD).&lt;h4>Methods&lt;/h4>Participants were randomized to ertugliflozin (5 or 15 mg/d) or placebo, and plasma samples for biomarker analysis were collected at baseline, 26 weeks, and 52 weeks.&lt;h4>Results&lt;/h4>Ertugliflozin-treated participants had lower plasma levels of kidney injury molecule-1 (KIM-1) at 26 weeks (&lt;i>P&lt;/i> = 0.044) and 52 weeks (&lt;i>P&lt;/i> = 0.007) a</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Aug</publication><modification>2026-05-08T20:56:10.935Z</modification><creation>2022-02-11T07:26:43.128Z</creation></dates><accession>S-EPMC8343791</accession><cross_references><pubmed>34386658</pubmed><doi>10.1016/j.ekir.2021.05.022</doi></cross_references></HashMap>