<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3(1)</volume><submitter>Hua JPY</submitter><funding>Department of Veterans Affairs Sierra Pacific Mental Illness Research, Education, and Clinical Center</funding><pubmed_abstract>Research has found strong evidence for common and distinct morphometric brain abnormality profiles in nonaffective psychosis (NAff-P) and affective psychosis (Aff-P). Due to chronicity and prolonged medication exposure confounds, it is crucial to examine structural morphometry early in the course of psychosis. Using Human Connectome Project-Early Psychosis data, multivariate profile analyses were implemented to examine regional profiles for cortical thickness, cortical surface area, subcortical volume, and ventricular volume in healthy control (HC; &lt;i>n&lt;/i> = 56), early illness NAff-P (&lt;i>n&lt;/i> = 83), and Aff-P (&lt;i>n&lt;/i> = 30) groups after accounting for normal aging. Associations with symptom severity, functioning, and cognition were also examined. Group regional profiles were significantly nonparallel and differed in level for cortical thickness (&lt;i>P&lt;/i> &lt; .001), with NAff-P having widespread cortical thinning relative to HC and Aff-P and some regions showing greater deficits than others. Significant nonparallelism of group regional profiles was also evident for cortical surface area (&lt;i>P&lt;/i> &lt; .006), with Aff-P and N-Aff-P differing from HC and from each other (&lt;i>P&lt;/i> &lt; .001). For subcortical volume, there was significant profile nonparallelism with NAff-P having an enlarged left pallidum and smaller accumbens and hippocampus (&lt;i>P&lt;/i> &lt; .028), and Aff-P having a smaller accumbens and amygdala (&lt;i>P&lt;/i> &lt; .006), relative to HC. NAff-P also had larger basal ganglia compared to Aff-P. Furthermore, NAff-P had enlarged ventricles (&lt;i>P&lt;/i> &lt; .055) compared to HC and Aff-P. Additionally, greater ventricular volume was associated with increased manic symptoms in NAff-P and Aff-P. Overall, this study found common and distinct regional morphometric profile abnormalities in early illness NAff-P and Aff-P, providing evidence for both shared and disease-specific pathophysiological processes.</pubmed_abstract><journal>Schizophrenia bulletin open</journal><pagination>sgac028</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11206002</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cortical and Subcortical Structural Morphometric Profiles in Individuals with Nonaffective and Affective Early Illness Psychosis.</pubmed_title><pmcid>PMC11206002</pmcid><pubmed_authors>Mathalon DH</pubmed_authors><pubmed_authors>Hua JPY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cortical and Subcortical Structural Morphometric Profiles in Individuals with Nonaffective and Affective Early Illness Psychosis.</name><description>Research has found strong evidence for common and distinct morphometric brain abnormality profiles in nonaffective psychosis (NAff-P) and affective psychosis (Aff-P). Due to chronicity and prolonged medication exposure confounds, it is crucial to examine structural morphometry early in the course of psychosis. Using Human Connectome Project-Early Psychosis data, multivariate profile analyses were implemented to examine regional profiles for cortical thickness, cortical surface area, subcortical volume, and ventricular volume in healthy control (HC; &lt;i>n&lt;/i> = 56), early illness NAff-P (&lt;i>n&lt;/i> = 83), and Aff-P (&lt;i>n&lt;/i> = 30) groups after accounting for normal aging. Associations with symptom severity, functioning, and cognition were also examined. Group regional profiles were significantly nonparallel and differed in level for cortical thickness (&lt;i>P&lt;/i> &lt; .001), with NAff-P having widespread cortical thinning relative to HC and Aff-P and some regions showing greater deficits than others. Significant nonparallelism of group regional profiles was also evident for cortical surface area (&lt;i>P&lt;/i> &lt; .006), with Aff-P and N-Aff-P differing from HC and from each other (&lt;i>P&lt;/i> &lt; .001). For subcortical volume, there was significant profile nonparallelism with NAff-P having an enlarged left pallidum and smaller accumbens and hippocampus (&lt;i>P&lt;/i> &lt; .028), and Aff-P having a smaller accumbens and amygdala (&lt;i>P&lt;/i> &lt; .006), relative to HC. NAff-P also had larger basal ganglia compared to Aff-P. Furthermore, NAff-P had enlarged ventricles (&lt;i>P&lt;/i> &lt; .055) compared to HC and Aff-P. Additionally, greater ventricular volume was associated with increased manic symptoms in NAff-P and Aff-P. Overall, this study found common and distinct regional morphometric profile abnormalities in early illness NAff-P and Aff-P, providing evidence for both shared and disease-specific pathophysiological processes.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2026-06-03T12:03:26.39Z</modification><creation>2025-04-05T10:09:26.189Z</creation></dates><accession>S-EPMC11206002</accession><cross_references><pubmed>39144757</pubmed><doi>10.1093/schizbullopen/sgac028</doi></cross_references></HashMap>