<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang L</submitter><funding>NIMH</funding><funding>American College of Clinical Pharmacy</funding><funding>NCATS NIH HHS</funding><funding>NIMH NIH HHS</funding><pagination>110464</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8932335</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>113</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Cognitive impairment is a core deficit across psychotic disorders, the causes and therapeutics of which remain unclear. Epidemiological observations have suggested associations between cognitive dysfunction in psychotic disorders and cardiovascular risk factors, but an underlying etiology has not been established.&lt;h4>Methods&lt;/h4>Neuropsychological performance using the Brief Assessment of Cognition in Schizophrenia (BACS) was assessed in 616 individuals of European ancestry (403 psychosis, 213 controls). Polygenic risk scores for coronary artery disease (PRS&lt;sub>CAD&lt;/sub>) were quantified for each participant across 13 p-value thresholds (P&lt;sub>T&lt;/sub> 0.5-5e&lt;sup>-8&lt;/sup>). Cardiovascular and psychotropic medications were categorized for association analyses. Each PRS&lt;su</pubmed_abstract><journal>Progress in neuro-psychopharmacology &amp; biological psychiatry</journal><pubmed_title>Impact of polygenic risk for coronary artery disease and cardiovascular medication burden on cognitive impairment in psychotic disorders.</pubmed_title><pmcid>PMC8932335</pmcid><funding_grant_id>R01 MH078113</funding_grant_id><funding_grant_id>MH-083126</funding_grant_id><funding_grant_id>R01 MH077852</funding_grant_id><funding_grant_id>R01 MH077851</funding_grant_id><funding_grant_id>R01 MH077862</funding_grant_id><funding_grant_id>MH-083888</funding_grant_id><funding_grant_id>K08 MH083888</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><funding_grant_id>K23 MH083126</funding_grant_id><funding_grant_id>R01 MH103368</funding_grant_id><funding_grant_id>K23 MH072767</funding_grant_id><funding_grant_id>MH-072767</funding_grant_id><funding_grant_id>MH-077945</funding_grant_id><funding_grant_id>MH-078113</funding_grant_id><funding_grant_id>R01 MH124813</funding_grant_id><funding_grant_id>R01 MH077945</funding_grant_id><funding_grant_id>MH-077852</funding_grant_id><funding_grant_id>MH-077862</funding_grant_id><funding_grant_id>MH-077851</funding_grant_id><funding_grant_id>R01 MH103366</funding_grant_id><pubmed_authors>Pearlson GD</pubmed_authors><pubmed_authors>Clementz BA</pubmed_authors><pubmed_authors>Hill SK</pubmed_authors><pubmed_authors>Keshavan MS</pubmed_authors><pubmed_authors>Ivleva EI</pubmed_authors><pubmed_authors>Keedy SK</pubmed_authors><pubmed_authors>Wu B</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Keefe RSE</pubmed_authors><pubmed_authors>Alliey-Rodriguez N</pubmed_authors><pubmed_authors>Tamminga CA</pubmed_authors><pubmed_authors>Gershon ES</pubmed_authors><pubmed_authors>Eum S</pubmed_authors><pubmed_authors>Lizano P</pubmed_authors><pubmed_authors>Reilly JL</pubmed_authors><pubmed_authors>Guo B</pubmed_authors><pubmed_authors>Sweeney JA</pubmed_authors><pubmed_authors>Bishop JR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of polygenic risk for coronary artery disease and cardiovascular medication burden on cognitive impairment in psychotic disorders.</name><description>&lt;h4>Background&lt;/h4>Cognitive impairment is a core deficit across psychotic disorders, the causes and therapeutics of which remain unclear. Epidemiological observations have suggested associations between cognitive dysfunction in psychotic disorders and cardiovascular risk factors, but an underlying etiology has not been established.&lt;h4>Methods&lt;/h4>Neuropsychological performance using the Brief Assessment of Cognition in Schizophrenia (BACS) was assessed in 616 individuals of European ancestry (403 psychosis, 213 controls). Polygenic risk scores for coronary artery disease (PRS&lt;sub>CAD&lt;/sub>) were quantified for each participant across 13 p-value thresholds (P&lt;sub>T&lt;/sub> 0.5-5e&lt;sup>-8&lt;/sup>). Cardiovascular and psychotropic medications were categorized for association analyses. Each PRS&lt;su</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-19T13:30:51.845Z</modification><creation>2025-04-19T13:30:51.845Z</creation></dates><accession>S-EPMC8932335</accession><cross_references><pubmed>34756932</pubmed><doi>10.1016/j.pnpbp.2021.110464</doi></cross_references></HashMap>