<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Forrester SN</submitter><funding>NCATS NIH HHS</funding><funding>NIA NIH HHS</funding><funding>National Heart, Lung, and Blood Institute</funding><funding>NHLBI NIH HHS</funding><funding>Center for Information Technology</funding><pagination>997-1009</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8137718</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(5)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Variability of Cardiovascular disease (CVD) risk, including racial difference, is not fully accounted for by the variability of traditional CVD risk factors. We used a multiple biomarker model as a framework to explore known racial differences in CVD burden.&lt;h4>Design&lt;/h4>We measured associations between accelerated aging (AccA) measured by a combination of biomarkers, and cardiovascular morbidity and all-cause mortality using data from the Coronary Artery Risk Development in Young Adults study (CARDIA). AccA was defined as the difference between biological age, calculated using biomarkers with the Klemera and Doubal method, and chronological age. Using logistic regression, we assessed overall and race-specific associations between AccA, CVD, and all-cause mortality.&lt;h4>R</pubmed_abstract><journal>Ethnicity &amp; health</journal><pubmed_title>Racial differences in the association of accelerated aging with future cardiovascular events and all-cause mortality: the coronary artery risk development in young adults study, 2007-2018.</pubmed_title><pmcid>PMC8137718</pmcid><funding_grant_id>HHSN268201800005I</funding_grant_id><funding_grant_id>HHSN268201800004I</funding_grant_id><funding_grant_id>K02AG059140,R01AG054363,U54MD00214</funding_grant_id><funding_grant_id>HHSN268201800007I</funding_grant_id><funding_grant_id>R01 AG054363</funding_grant_id><funding_grant_id>HHSN268201800006I</funding_grant_id><funding_grant_id>5T32HL120823-02</funding_grant_id><funding_grant_id>K02 AG059140</funding_grant_id><funding_grant_id>HHSN268201800003I</funding_grant_id><funding_grant_id>UL1 TR001453</funding_grant_id><funding_grant_id>T32 HL120823</funding_grant_id><funding_grant_id>KL2 TR001455</funding_grant_id><pubmed_authors>Forrester SN</pubmed_authors><pubmed_authors>Roger VL</pubmed_authors><pubmed_authors>Schreiner PJ</pubmed_authors><pubmed_authors>Kiefe CI</pubmed_authors><pubmed_authors>Jacobs DR</pubmed_authors><pubmed_authors>Zmora R</pubmed_authors><pubmed_authors>Thorpe RJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Racial differences in the association of accelerated aging with future cardiovascular events and all-cause mortality: the coronary artery risk development in young adults study, 2007-2018.</name><description>&lt;h4>Objective&lt;/h4>Variability of Cardiovascular disease (CVD) risk, including racial difference, is not fully accounted for by the variability of traditional CVD risk factors. We used a multiple biomarker model as a framework to explore known racial differences in CVD burden.&lt;h4>Design&lt;/h4>We measured associations between accelerated aging (AccA) measured by a combination of biomarkers, and cardiovascular morbidity and all-cause mortality using data from the Coronary Artery Risk Development in Young Adults study (CARDIA). AccA was defined as the difference between biological age, calculated using biomarkers with the Klemera and Doubal method, and chronological age. Using logistic regression, we assessed overall and race-specific associations between AccA, CVD, and all-cause mortality.&lt;h4>R</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2025-04-22T07:30:15.837Z</modification><creation>2022-07-07T22:42:06.515Z</creation></dates><accession>S-EPMC8137718</accession><cross_references><pubmed>33222499</pubmed><doi>10.1080/13557858.2020.1839021</doi></cross_references></HashMap>