<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Deng LR</submitter><funding>BLRD VA</funding><funding>NIDCR NIH HHS</funding><funding>NIBIB NIH HHS</funding><funding>NICHD NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NIDA NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>National Institutes of Health Office of the Director</funding><funding>National Institutes of Health</funding><funding>US Department of Veterans Affairs</funding><funding>NLM NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>Roy J. Carver Charitable Trust</funding><funding>NCI NIH HHS</funding><funding>National Institute of Mental Health</funding><funding>National Institute on Drug Abuse</funding><funding>NIH HHS</funding><pagination>448-460</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11560692</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>368</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Bipolar disorder (BD) is a chronic psychiatric mood disorder that is solely diagnosed based on clinical symptoms. These symptoms often overlap with other psychiatric disorders. Efforts to use machine learning (ML) to create predictive models for BD based on data from brain imaging are expanding but have often been limited using only a single modality and the exclusion of the cerebellum, which may be relevant in BD.&lt;h4>Methods&lt;/h4>In this study, we sought to improve ML classification of BD by combining information from structural, functional, and diffusion-weighted imaging. Participants (108 BD I, 78 control) with BD type I and matched controls were recruited into an imaging study. This dataset was randomly divided into training and testing sets. For each of the three mod</pubmed_abstract><journal>Journal of affective disorders</journal><pubmed_title>Machine learning with multiple modalities of brain magnetic resonance imaging data to identify the presence of bipolar disorder.</pubmed_title><pmcid>PMC11560692</pmcid><funding_grant_id>R01 DA052953</funding_grant_id><funding_grant_id>UM1 TR004403</funding_grant_id><funding_grant_id>RL1MH083268</funding_grant_id><funding_grant_id>RL1MH083269</funding_grant_id><funding_grant_id>RL1 DA024853</funding_grant_id><funding_grant_id>R01MH125838</funding_grant_id><funding_grant_id>PL1 NS062410</funding_grant_id><funding_grant_id>UL1 TR002537</funding_grant_id><funding_grant_id>IO1BX004440</funding_grant_id><funding_grant_id>R01 EB031169</funding_grant_id><funding_grant_id>R01MH111578</funding_grant_id><funding_grant_id>T32 MH019113</funding_grant_id><funding_grant_id>I01 BX004440</funding_grant_id><funding_grant_id>P30 CA086862</funding_grant_id><funding_grant_id>S10OD025025</funding_grant_id><funding_grant_id>RL1 MH083270</funding_grant_id><funding_grant_id>P50HD103556</funding_grant_id><funding_grant_id>RL1LM009833</funding_grant_id><funding_grant_id>S10RR028821</funding_grant_id><funding_grant_id>RL1 LM009833</funding_grant_id><funding_grant_id>S10 OD030220</funding_grant_id><funding_grant_id>R01 MH125838</funding_grant_id><funding_grant_id>KL2TR002537</funding_grant_id><funding_grant_id>R01 MH111578</funding_grant_id><funding_grant_id>RL1MH083270</funding_grant_id><funding_grant_id>UL1 DE019580</funding_grant_id><funding_grant_id>PL1 MH083271</funding_grant_id><funding_grant_id>T32MH019113</funding_grant_id><funding_grant_id>RL1 MH083268</funding_grant_id><funding_grant_id>R01DA052953</funding_grant_id><funding_grant_id>RL1DA024853</funding_grant_id><funding_grant_id>P50 HD103556</funding_grant_id><funding_grant_id>RL1 MH083269</funding_grant_id><funding_grant_id>UL1DE019580</funding_grant_id><funding_grant_id>PL1NS062410</funding_grant_id><funding_grant_id>S10 RR028821</funding_grant_id><funding_grant_id>S10 OD025025</funding_grant_id><funding_grant_id>UM1TR004403</funding_grant_id><funding_grant_id>PL1MH083271</funding_grant_id><pubmed_authors>Magnotta VA</pubmed_authors><pubmed_authors>Williams AJ</pubmed_authors><pubmed_authors>Barsotti EJ</pubmed_authors><pubmed_authors>Fiedorowicz JG</pubmed_authors><pubmed_authors>Rivera-Dompenciel AM</pubmed_authors><pubmed_authors>Richards JG</pubmed_authors><pubmed_authors>Sathyaputri L</pubmed_authors><pubmed_authors>Xu J</pubmed_authors><pubmed_authors>Deng LR</pubmed_authors><pubmed_authors>Mani M</pubmed_authors><pubmed_authors>Abdolmotalleby H</pubmed_authors><pubmed_authors>Saleem A</pubmed_authors><pubmed_authors>Wemmie JA</pubmed_authors><pubmed_authors>Christensen GE</pubmed_authors><pubmed_authors>Voss MW</pubmed_authors><pubmed_authors>Shaffer JJ</pubmed_authors><pubmed_authors>Harmata GIS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Machine learning with multiple modalities of brain magnetic resonance imaging data to identify the presence of bipolar disorder.</name><description>&lt;h4>Background&lt;/h4>Bipolar disorder (BD) is a chronic psychiatric mood disorder that is solely diagnosed based on clinical symptoms. These symptoms often overlap with other psychiatric disorders. Efforts to use machine learning (ML) to create predictive models for BD based on data from brain imaging are expanding but have often been limited using only a single modality and the exclusion of the cerebellum, which may be relevant in BD.&lt;h4>Methods&lt;/h4>In this study, we sought to improve ML classification of BD by combining information from structural, functional, and diffusion-weighted imaging. Participants (108 BD I, 78 control) with BD type I and matched controls were recruited into an imaging study. This dataset was randomly divided into training and testing sets. For each of the three mod</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2026-06-06T17:27:47.551Z</modification><creation>2026-06-03T03:10:37.803Z</creation></dates><accession>S-EPMC11560692</accession><cross_references><pubmed>39278469</pubmed><doi>10.1016/j.jad.2024.09.025</doi></cross_references></HashMap>