<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Manubolu VS</submitter><funding>National Center for Advancing Translational Sciences</funding><funding>NCATS NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>National Heart, Lung, and Blood Institute</funding><funding>National Institutes of Health</funding><funding>NIAMS NIH HHS</funding><pagination>532-540</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9974807</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(3)</volume><pubmed_abstract>&lt;h4>Background and aims&lt;/h4>Previously, osteoporosis and coronary artery disease were considered unrelated. However, beyond age, these two conditions appear to share common etiologies that are not yet fully understood. We examined the relationship between thoracic spine bone mineral density (BMD) and severity of coronary artery calcium (CAC) score.&lt;h4>Methods and results&lt;/h4>MESA is a prospective cohort study of 6814 men and women between the ages of 45 and 84 years, without clinical cardiovascular disease. This study included participants who underwent non-contrast chest CT scans to determine CAC score and thoracic spine BMD. The thoracic spine BMD was categorized into osteoporosis (defined as T score: ≤ -2.5), osteopenia (T-score between: -2.5 and -1) and normal BMD (T-score ≥ -1). There</pubmed_abstract><journal>Nutrition, metabolism, and cardiovascular diseases : NMCD</journal><pubmed_title>Association between coronary artery calcium and thoracic spine bone mineral density: Multiethnic Study of Atherosclerosis (MESA).</pubmed_title><pmcid>PMC9974807</pmcid><funding_grant_id>R42 AR070713</funding_grant_id><funding_grant_id>UL1-TR-001079</funding_grant_id><funding_grant_id>UL1-TR-000040</funding_grant_id><funding_grant_id>UL1 TR001420</funding_grant_id><funding_grant_id>N01-HC-95161</funding_grant_id><funding_grant_id>N01 HC095166</funding_grant_id><funding_grant_id>N01 HC095165</funding_grant_id><funding_grant_id>N01-HC-95162</funding_grant_id><funding_grant_id>N01-HC-95163</funding_grant_id><funding_grant_id>N01 HC095168</funding_grant_id><funding_grant_id>N01-HC-95164</funding_grant_id><funding_grant_id>N01 HC095167</funding_grant_id><funding_grant_id>N01 HC095169</funding_grant_id><funding_grant_id>N01-HC-95160</funding_grant_id><funding_grant_id>N01-HC-95159</funding_grant_id><funding_grant_id>2R42AR070713</funding_grant_id><funding_grant_id>75N92020D00007</funding_grant_id><funding_grant_id>N01 HC095160</funding_grant_id><funding_grant_id>N01 HC095162</funding_grant_id><funding_grant_id>N01 HC095161</funding_grant_id><funding_grant_id>N01 HC095164</funding_grant_id><funding_grant_id>N01 HC095163</funding_grant_id><funding_grant_id>75N92020D00001</funding_grant_id><funding_grant_id>75N92020D00002</funding_grant_id><funding_grant_id>75N92020D00005</funding_grant_id><funding_grant_id>R01 HL071739</funding_grant_id><funding_grant_id>75N92020D00006</funding_grant_id><funding_grant_id>75N92020D00003</funding_grant_id><funding_grant_id>75N92020D00004</funding_grant_id><funding_grant_id>UL1 TR000040</funding_grant_id><funding_grant_id>UL1-TR-001420</funding_grant_id><funding_grant_id>HHSN268201500003C</funding_grant_id><funding_grant_id>UL1 TR001079</funding_grant_id><funding_grant_id>N01 HC095159</funding_grant_id><funding_grant_id>N01-HC-95169</funding_grant_id><funding_grant_id>R01 HL146666</funding_grant_id><funding_grant_id>N01-HC-95165</funding_grant_id><funding_grant_id>N01-HC-95166</funding_grant_id><funding_grant_id>N01-HC-95167</funding_grant_id><funding_grant_id>N01-HC-95168</funding_grant_id><funding_grant_id>HHSN268201500003I</funding_grant_id><pubmed_authors>Carr JJ</pubmed_authors><pubmed_authors>Dailing C</pubmed_authors><pubmed_authors>Mao S</pubmed_authors><pubmed_authors>Havistin R</pubmed_authors><pubmed_authors>Kinninger A</pubmed_authors><pubmed_authors>Gao Y</pubmed_authors><pubmed_authors>Dahal S</pubmed_authors><pubmed_authors>Budoff MJ</pubmed_authors><pubmed_authors>Roy SK</pubmed_authors><pubmed_authors>Ahmad K</pubmed_authors><pubmed_authors>Manubolu VS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association between coronary artery calcium and thoracic spine bone mineral density: Multiethnic Study of Atherosclerosis (MESA).</name><description>&lt;h4>Background and aims&lt;/h4>Previously, osteoporosis and coronary artery disease were considered unrelated. However, beyond age, these two conditions appear to share common etiologies that are not yet fully understood. We examined the relationship between thoracic spine bone mineral density (BMD) and severity of coronary artery calcium (CAC) score.&lt;h4>Methods and results&lt;/h4>MESA is a prospective cohort study of 6814 men and women between the ages of 45 and 84 years, without clinical cardiovascular disease. This study included participants who underwent non-contrast chest CT scans to determine CAC score and thoracic spine BMD. The thoracic spine BMD was categorized into osteoporosis (defined as T score: ≤ -2.5), osteopenia (T-score between: -2.5 and -1) and normal BMD (T-score ≥ -1). There</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2026-06-04T05:53:39.903Z</modification><creation>2025-04-06T11:04:02.724Z</creation></dates><accession>S-EPMC9974807</accession><cross_references><pubmed>36642601</pubmed><doi>10.1016/j.numecd.2022.12.006</doi></cross_references></HashMap>