<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Segar MW</submitter><funding>NCATS NIH HHS</funding><funding>NIA NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NIMHD NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>2370-2383</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9976274</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>143(24)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Heart failure (HF) risk and the underlying risk factors vary by race. Traditional models for HF risk prediction treat race as a covariate in risk prediction and do not account for significant parameters such as cardiac biomarkers. Machine learning (ML) may offer advantages over traditional modeling techniques to develop race-specific HF risk prediction models and to elucidate important contributors of HF development across races.&lt;h4>Methods&lt;/h4>We performed a retrospective analysis of 4 large, community cohort studies (ARIC [Atherosclerosis Risk in Communities], DHS [Dallas Heart Study], JHS [Jackson Heart Study], and MESA [Multi-Ethnic Study of Atherosclerosis]) with adjudicated HF events. The study included participants who were >40 years of age and free of HF at basel</pubmed_abstract><journal>Circulation</journal><pubmed_title>Development and Validation of Machine Learning-Based Race-Specific Models to Predict 10-Year Risk of Heart Failure: A Multicohort Analysis.</pubmed_title><pmcid>PMC9976274</pmcid><funding_grant_id>HHSN268201100011I</funding_grant_id><funding_grant_id>R01 HL134320</funding_grant_id><funding_grant_id>R03 AG067960</funding_grant_id><funding_grant_id>UL1 TR001105</funding_grant_id><funding_grant_id>HHSN261201800014I</funding_grant_id><funding_grant_id>HHSN268201800014C</funding_grant_id><funding_grant_id>N01HC95159</funding_grant_id><funding_grant_id>HHSN261201800010I</funding_grant_id><funding_grant_id>HHSN268201100009I</funding_grant_id><funding_grant_id>HHSN268201800012C</funding_grant_id><funding_grant_id>R01 HL117323</funding_grant_id><funding_grant_id>HHSN268201100005C</funding_grant_id><funding_grant_id>HHSN268201800012I</funding_grant_id><funding_grant_id>HHSN268201100007C</funding_grant_id><funding_grant_id>HHSN268201800014I</funding_grant_id><funding_grant_id>HHSN268201100009C</funding_grant_id><funding_grant_id>HHSN268201800010I</funding_grant_id><funding_grant_id>HHSN268201100011C</funding_grant_id><funding_grant_id>HHSN268201100005I</funding_grant_id><funding_grant_id>HHSN268201100005G</funding_grant_id><funding_grant_id>HHSN268201100007I</funding_grant_id><funding_grant_id>N01HC95160</funding_grant_id><funding_grant_id>N01HC95161</funding_grant_id><funding_grant_id>N01HC95162</funding_grant_id><funding_grant_id>N01HC95163</funding_grant_id><funding_grant_id>N01HC95164</funding_grant_id><funding_grant_id>N01HC95165</funding_grant_id><funding_grant_id>N01HC95169</funding_grant_id><funding_grant_id>HHSN268201800015I</funding_grant_id><funding_grant_id>HHSN268201100006C</funding_grant_id><funding_grant_id>HHSN268201800011C</funding_grant_id><funding_grant_id>HHSN268201100008C</funding_grant_id><funding_grant_id>HHSN268201800011I</funding_grant_id><funding_grant_id>T32 HL125247</funding_grant_id><funding_grant_id>HHSN268201800013I</funding_grant_id><funding_grant_id>KL2 TR002490</funding_grant_id><funding_grant_id>HHSN268201100010C</funding_grant_id><funding_grant_id>HHSN268201100008I</funding_grant_id><funding_grant_id>HHSN268201100012C</funding_grant_id><pubmed_authors>Segar MW</pubmed_authors><pubmed_authors>Rao S</pubmed_authors><pubmed_authors>Lewis AA</pubmed_authors><pubmed_authors>Rodriguez CJ</pubmed_authors><pubmed_authors>Mentz RJ</pubmed_authors><pubmed_authors>de Lemos JA</pubmed_authors><pubmed_authors>Ayers C</pubmed_authors><pubmed_authors>Ballantyne CM</pubmed_authors><pubmed_authors>Raffield LM</pubmed_authors><pubmed_authors>Correa A</pubmed_authors><pubmed_authors>Chandra A</pubmed_authors><pubmed_authors>Patel KV</pubmed_authors><pubmed_authors>Jaeger BC</pubmed_authors><pubmed_authors>Nambi V</pubmed_authors><pubmed_authors>Ndumele CE</pubmed_authors><pubmed_authors>Hall ME</pubmed_authors><pubmed_authors>Butler J</pubmed_authors><pubmed_authors>Michos ED</pubmed_authors><pubmed_authors>Pandey A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development and Validation of Machine Learning-Based Race-Specific Models to Predict 10-Year Risk of Heart Failure: A Multicohort Analysis.</name><description>&lt;h4>Background&lt;/h4>Heart failure (HF) risk and the underlying risk factors vary by race. Traditional models for HF risk prediction treat race as a covariate in risk prediction and do not account for significant parameters such as cardiac biomarkers. Machine learning (ML) may offer advantages over traditional modeling techniques to develop race-specific HF risk prediction models and to elucidate important contributors of HF development across races.&lt;h4>Methods&lt;/h4>We performed a retrospective analysis of 4 large, community cohort studies (ARIC [Atherosclerosis Risk in Communities], DHS [Dallas Heart Study], JHS [Jackson Heart Study], and MESA [Multi-Ethnic Study of Atherosclerosis]) with adjudicated HF events. The study included participants who were >40 years of age and free of HF at basel</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jun</publication><modification>2025-04-04T00:35:47.66Z</modification><creation>2025-04-04T00:35:47.66Z</creation></dates><accession>S-EPMC9976274</accession><cross_references><pubmed>33845593</pubmed><doi>10.1161/circulationaha.120.053134</doi><doi>10.1161/CIRCULATIONAHA.120.053134</doi></cross_references></HashMap>