<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rao VS</submitter><funding>NHLBI NIH HHS</funding><funding>National Institutes of Health</funding><funding>AstraZeneca</funding><pagination>340-346</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10947725</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(2)</volume><pubmed_abstract>&lt;h4>Background and objectives&lt;/h4>Approaches to distinguishing pathological cardiorenal dysfunction in heart failure (HF) from functional/hemodynamically mediated changes in serum creatinine are needed. We investigated urine galectin-3 as a candidate biomarker of renal fibrosis and a prognostic indicator of cardiorenal dysfunction phenotypes.&lt;h4>Methods&lt;/h4>We measured urine galectin-3 in 2 contemporary HF cohorts: the Yale Transitional Care Clinic (YTCC) cohort (n = 132) and the Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist (TOPCAT) trial (n = 434). We assessed the association of urine galectin-3 with all-cause mortality in both cohorts and the association with an established marker of renal tissue fibrosis, urinary amino-terminal propeptide of type </pubmed_abstract><journal>Journal of cardiac failure</journal><pubmed_title>Association of Urine Galectin-3 With Cardiorenal Outcomes in Patients With Heart Failure.</pubmed_title><pmcid>PMC10947725</pmcid><funding_grant_id>R21 HL143092</funding_grant_id><funding_grant_id>K23 HL114868</funding_grant_id><funding_grant_id>L30 HL115790</funding_grant_id><funding_grant_id>R01HL128973</funding_grant_id><funding_grant_id>R01 HL128973</funding_grant_id><funding_grant_id>L30HL115790</funding_grant_id><funding_grant_id>R01HL148354</funding_grant_id><funding_grant_id>K23HL114868</funding_grant_id><funding_grant_id>R01HL139629</funding_grant_id><funding_grant_id>R01 HL148354</funding_grant_id><funding_grant_id>R21HL143092</funding_grant_id><funding_grant_id>R01 HL139629</funding_grant_id><pubmed_authors>Cox ZL</pubmed_authors><pubmed_authors>Ivey-Miranda JB</pubmed_authors><pubmed_authors>Moreno-Villagomez J</pubmed_authors><pubmed_authors>Rao VS</pubmed_authors><pubmed_authors>Testani JM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association of Urine Galectin-3 With Cardiorenal Outcomes in Patients With Heart Failure.</name><description>&lt;h4>Background and objectives&lt;/h4>Approaches to distinguishing pathological cardiorenal dysfunction in heart failure (HF) from functional/hemodynamically mediated changes in serum creatinine are needed. We investigated urine galectin-3 as a candidate biomarker of renal fibrosis and a prognostic indicator of cardiorenal dysfunction phenotypes.&lt;h4>Methods&lt;/h4>We measured urine galectin-3 in 2 contemporary HF cohorts: the Yale Transitional Care Clinic (YTCC) cohort (n = 132) and the Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist (TOPCAT) trial (n = 434). We assessed the association of urine galectin-3 with all-cause mortality in both cohorts and the association with an established marker of renal tissue fibrosis, urinary amino-terminal propeptide of type </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2025-04-05T10:19:40.313Z</modification><creation>2025-04-05T10:19:40.313Z</creation></dates><accession>S-EPMC10947725</accession><cross_references><pubmed>37301248</pubmed><doi>10.1016/j.cardfail.2023.05.018</doi></cross_references></HashMap>