<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>19</volume><submitter>Nallamshetty S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Our understanding of the factors associated with improvement of LVEF and a heart failure with improved EF (HFimpEF) phenotype remains incomplete.&lt;h4>Methods&lt;/h4>We conducted a retrospective study using a national database of patients followed in the Veterans Affairs (VA) health system with serial assessment of left ventricular ejection fraction (LVEF) by echocardiography. We identified US veterans with a new diagnosis of heart failure with: (i) LVEF of &lt;40 % in the 12 months prior to diagnosis, and (ii) follow-up LVEF assessment at least 6 months after their diagnosis. We defined HFimpEF as a final LVEF of ≥40 %.&lt;h4>Results&lt;/h4>Among the 106,414 US veterans with an initial LVEF of &lt;40 % in this analysis, 39,994 (37.6 %) had a final EF of >40 % after a median follow up of 5 years. Multivariate regression analysis identified several factors that were independently associated with LVEF improvement including female sex, younger age, higher BMI, and a history of specific comorbid conditions such as hypertension, valve disease, atrial fibrillation, connective tissue disease, liver disease, and malignancy (p &lt; 0.001). Conversely, a history of ischemic heart disease and peripheral arterial disease, as well as specific racial backgrounds (Black and Hispanic) were associated with lower rates of LVEF improvement. The model c-statistic for predicting LVEF improvement was 0.70.&lt;h4>Conclusions&lt;/h4>This large, detailed dataset facilitated an analysis of a large number of variables that significantly associated with HFimpEF; however, their combined discriminatory value for LVEF improvement remained modest, underscoring the complexity of the gene-environment-treatment interactions that govern LV function.</pubmed_abstract><journal>American heart journal plus : cardiology research and practice</journal><pagination>100183</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10978352</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinical predictors of improvement in left ventricular ejection fraction in U.S. veterans with heart failure.</pubmed_title><pmcid>PMC10978352</pmcid><pubmed_authors>Nallamshetty S</pubmed_authors><pubmed_authors>Castillo A</pubmed_authors><pubmed_authors>Haddad F</pubmed_authors><pubmed_authors>Nguyen A</pubmed_authors><pubmed_authors>Heidenreich P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical predictors of improvement in left ventricular ejection fraction in U.S. veterans with heart failure.</name><description>&lt;h4>Background&lt;/h4>Our understanding of the factors associated with improvement of LVEF and a heart failure with improved EF (HFimpEF) phenotype remains incomplete.&lt;h4>Methods&lt;/h4>We conducted a retrospective study using a national database of patients followed in the Veterans Affairs (VA) health system with serial assessment of left ventricular ejection fraction (LVEF) by echocardiography. We identified US veterans with a new diagnosis of heart failure with: (i) LVEF of &lt;40 % in the 12 months prior to diagnosis, and (ii) follow-up LVEF assessment at least 6 months after their diagnosis. We defined HFimpEF as a final LVEF of ≥40 %.&lt;h4>Results&lt;/h4>Among the 106,414 US veterans with an initial LVEF of &lt;40 % in this analysis, 39,994 (37.6 %) had a final EF of >40 % after a median follow up of 5 years. Multivariate regression analysis identified several factors that were independently associated with LVEF improvement including female sex, younger age, higher BMI, and a history of specific comorbid conditions such as hypertension, valve disease, atrial fibrillation, connective tissue disease, liver disease, and malignancy (p &lt; 0.001). Conversely, a history of ischemic heart disease and peripheral arterial disease, as well as specific racial backgrounds (Black and Hispanic) were associated with lower rates of LVEF improvement. The model c-statistic for predicting LVEF improvement was 0.70.&lt;h4>Conclusions&lt;/h4>This large, detailed dataset facilitated an analysis of a large number of variables that significantly associated with HFimpEF; however, their combined discriminatory value for LVEF improvement remained modest, underscoring the complexity of the gene-environment-treatment interactions that govern LV function.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2025-04-22T08:23:49.611Z</modification><creation>2025-04-05T22:31:14.314Z</creation></dates><accession>S-EPMC10978352</accession><cross_references><pubmed>38558863</pubmed><doi>10.1016/j.ahjo.2022.100183</doi></cross_references></HashMap>