<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kamimura D</submitter><funding>Jackson State University</funding><funding>NIDDK NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>NHLBI NIH HHS</funding><funding>NIMHD NIH HHS</funding><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><pagination>901-911</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8026689</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>96(4)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To examine associations between physical activity (PA), inflammation, coronary artery calcification (CAC), and incident coronary heart disease (CHD) in African Americans.&lt;h4>Methods&lt;/h4>Among Jackson Heart Study participants without prevalent CHD at baseline (n=4295), we examined the relationships between PA and high-sensitivity C-reactive protein, the presence of CAC (Agatston score ≥100), and incident CHD. Based on the American Heart Association's Life's Simple 7 metrics, participants were classified as having poor, intermediate, or ideal PA.&lt;h4>Results&lt;/h4>After adjustment for possible confounding factors, ideal PA was associated with lower high-sensitivity C-reactive protein levels (β, -0.15; 95% CI, -0.15 to -0.002) and a lower prevalence of CAC (odds ratio, 0.70; 95</pubmed_abstract><journal>Mayo Clinic proceedings</journal><pubmed_title>Physical Activity, Inflammation, Coronary Artery Calcification, and Incident Coronary Heart Disease in African Americans: Insights From the Jackson Heart Study.</pubmed_title><pmcid>PMC8026689</pmcid><funding_grant_id>HHSN268201800015I</funding_grant_id><funding_grant_id>HHSN268201800012C</funding_grant_id><funding_grant_id>HHSN268201800011C</funding_grant_id><funding_grant_id>P20 GM104357</funding_grant_id><funding_grant_id>HHSN268201800013I</funding_grant_id><funding_grant_id>U54 GM104940</funding_grant_id><funding_grant_id>K08 DK099415</funding_grant_id><funding_grant_id>HHSN268201800014C</funding_grant_id><funding_grant_id>U54 GM115428</funding_grant_id><pubmed_authors>Suzuki T</pubmed_authors><pubmed_authors>Guild CS</pubmed_authors><pubmed_authors>Loprinzi PD</pubmed_authors><pubmed_authors>Oshunbade AA</pubmed_authors><pubmed_authors>Hall JE</pubmed_authors><pubmed_authors>Correa A</pubmed_authors><pubmed_authors>Kamimura D</pubmed_authors><pubmed_authors>Clark D</pubmed_authors><pubmed_authors>Cain-Shields LR</pubmed_authors><pubmed_authors>Ashley KE</pubmed_authors><pubmed_authors>Hall ME</pubmed_authors><pubmed_authors>Blaha MJ</pubmed_authors><pubmed_authors>Butler J</pubmed_authors><pubmed_authors>Newton R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Physical Activity, Inflammation, Coronary Artery Calcification, and Incident Coronary Heart Disease in African Americans: Insights From the Jackson Heart Study.</name><description>&lt;h4>Objective&lt;/h4>To examine associations between physical activity (PA), inflammation, coronary artery calcification (CAC), and incident coronary heart disease (CHD) in African Americans.&lt;h4>Methods&lt;/h4>Among Jackson Heart Study participants without prevalent CHD at baseline (n=4295), we examined the relationships between PA and high-sensitivity C-reactive protein, the presence of CAC (Agatston score ≥100), and incident CHD. Based on the American Heart Association's Life's Simple 7 metrics, participants were classified as having poor, intermediate, or ideal PA.&lt;h4>Results&lt;/h4>After adjustment for possible confounding factors, ideal PA was associated with lower high-sensitivity C-reactive protein levels (β, -0.15; 95% CI, -0.15 to -0.002) and a lower prevalence of CAC (odds ratio, 0.70; 95</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2025-04-29T11:30:41.939Z</modification><creation>2025-04-06T19:55:11.496Z</creation></dates><accession>S-EPMC8026689</accession><cross_references><pubmed>33714604</pubmed><doi>10.1016/j.mayocp.2020.09.042</doi></cross_references></HashMap>