<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Miley KM</submitter><funding>NIMH NIH HHS</funding><funding>National Institute of Mental Health</funding><pagination>139-147</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10936711</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>85</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To estimate 30-year CVD risk and modifiable risk factors in young adults with serious mental illness (SMI) versus those without, and assess variations in CVD risk by race, ethnicity, and sex.&lt;h4>Method&lt;/h4>In this cross-sectional study, we estimated and compared the Framingham 30-year CVD risk score and individual modifiable CVD risk factors in young adult (20-39 years) primary care patients with and without SMI at two US healthcare systems (January 2016-Septemeber 2018). Interaction terms assessed whether the SMI-risk association differed across demographic groups.&lt;h4>Results&lt;/h4>Covariate-adjusted 30-year CVD risk was significantly higher for those with (n=4228) versus those without (n=155,363) SMI (RR 1.28, 95% CI [1.26, 1.30]). Patients with SMI had higher rates of hypertension (OR 2.02 [1.7, 2.39]), diabetes (OR 3.14 [2.59, 3.82]), obesity (OR 1.93 [1.8, 2.07]), and smoking (OR 4.94 [4.6, 5.36]). The increased 30-year CVD risk associated with SMI varied significantly by race and sex: there was an 8% higher risk in Black compared to White patients (RR 1.08, [1.04, 1.12]) and a 9% lower risk in men compared to women (RR 0.91 [0.88, 0.94]).&lt;h4>Conclusions&lt;/h4>Young adults with SMI are at increased 30-year risk of CVD, and further disparities exist for Black individuals and women.</pubmed_abstract><journal>General hospital psychiatry</journal><pubmed_title>30-year Cardiovascular Disease Risk for Young Adults with Serious Mental Illness.</pubmed_title><pmcid>PMC10936711</pmcid><funding_grant_id>U19 MH092201</funding_grant_id><funding_grant_id>U19MH092201</funding_grant_id><pubmed_authors>Rossom RC</pubmed_authors><pubmed_authors>Hooker SA</pubmed_authors><pubmed_authors>Crain AL</pubmed_authors><pubmed_authors>O'Connor PJ</pubmed_authors><pubmed_authors>Haapala JL</pubmed_authors><pubmed_authors>Bond DJ</pubmed_authors><pubmed_authors>Miley KM</pubmed_authors></additional><is_claimable>false</is_claimable><name>30-year Cardiovascular Disease Risk for Young Adults with Serious Mental Illness.</name><description>&lt;h4>Objective&lt;/h4>To estimate 30-year CVD risk and modifiable risk factors in young adults with serious mental illness (SMI) versus those without, and assess variations in CVD risk by race, ethnicity, and sex.&lt;h4>Method&lt;/h4>In this cross-sectional study, we estimated and compared the Framingham 30-year CVD risk score and individual modifiable CVD risk factors in young adult (20-39 years) primary care patients with and without SMI at two US healthcare systems (January 2016-Septemeber 2018). Interaction terms assessed whether the SMI-risk association differed across demographic groups.&lt;h4>Results&lt;/h4>Covariate-adjusted 30-year CVD risk was significantly higher for those with (n=4228) versus those without (n=155,363) SMI (RR 1.28, 95% CI [1.26, 1.30]). Patients with SMI had higher rates of hypertension (OR 2.02 [1.7, 2.39]), diabetes (OR 3.14 [2.59, 3.82]), obesity (OR 1.93 [1.8, 2.07]), and smoking (OR 4.94 [4.6, 5.36]). The increased 30-year CVD risk associated with SMI varied significantly by race and sex: there was an 8% higher risk in Black compared to White patients (RR 1.08, [1.04, 1.12]) and a 9% lower risk in men compared to women (RR 0.91 [0.88, 0.94]).&lt;h4>Conclusions&lt;/h4>Young adults with SMI are at increased 30-year risk of CVD, and further disparities exist for Black individuals and women.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov-Dec</publication><modification>2025-04-19T18:12:05.799Z</modification><creation>2025-04-19T18:12:05.799Z</creation></dates><accession>S-EPMC10936711</accession><cross_references><pubmed>38487652</pubmed><doi>10.1016/j.genhosppsych.2023.10.015</doi></cross_references></HashMap>