<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fan F</submitter><funding>Beijing Municipal Natural Science Foundation</funding><funding>NIMH NIH HHS</funding><funding>National Natural Science Foundation of China</funding><funding>Beijing Hospitals Authority Youth Programme</funding><funding>Capital's Funds for Health Improvement and Research</funding><funding>Cultivation Program of Beijing Municipal Hospital Administration</funding><funding>National Institute of Health grant</funding><funding>NIH HHS</funding><pagination>12-19</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9812867</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>77(1)</volume><pubmed_abstract>&lt;h4>Aim&lt;/h4>Approximately a third of patients with schizophrenia fail to adequately respond to antipsychotic medications, a condition known as treatment resistance (TR). We aimed to assess cognitive and cortical thickness deficits and their relationship to TR in schizophrenia.&lt;h4>Method&lt;/h4>We recruited patients with schizophrenia (n = 127), including patients at treatment initiation (n = 45), treatment-responsive patients (n = 40) and TR patients (n = 42), and healthy controls (n = 83). Clinical symptoms, neurocognitive function, and structural images were assessed. We performed group comparisons, and explored association of cortical thickness and cognition with TR.&lt;h4>Results&lt;/h4>The TR patients showed significantly more severe clinical symptoms and cognitive impairment relative to the t</pubmed_abstract><journal>Psychiatry and clinical neurosciences</journal><pubmed_title>Association of cortical thickness and cognition with schizophrenia treatment resistance.</pubmed_title><pmcid>PMC9812867</pmcid><funding_grant_id>PX2018069</funding_grant_id><funding_grant_id>2018-4-2133</funding_grant_id><funding_grant_id>31671145</funding_grant_id><funding_grant_id>S10 OD023696</funding_grant_id><funding_grant_id>QML20202001</funding_grant_id><funding_grant_id>81401115</funding_grant_id><funding_grant_id>81761128021</funding_grant_id><funding_grant_id>RF1 MH123163</funding_grant_id><funding_grant_id>R01MH112180</funding_grant_id><funding_grant_id>R01 MH112180</funding_grant_id><funding_grant_id>7182074</funding_grant_id><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Tian B</pubmed_authors><pubmed_authors>Du X</pubmed_authors><pubmed_authors>Yang F</pubmed_authors><pubmed_authors>Kochunov P</pubmed_authors><pubmed_authors>Fan F</pubmed_authors><pubmed_authors>Hong LE</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Hare S</pubmed_authors><pubmed_authors>Tan Y</pubmed_authors><pubmed_authors>Tan S</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association of cortical thickness and cognition with schizophrenia treatment resistance.</name><description>&lt;h4>Aim&lt;/h4>Approximately a third of patients with schizophrenia fail to adequately respond to antipsychotic medications, a condition known as treatment resistance (TR). We aimed to assess cognitive and cortical thickness deficits and their relationship to TR in schizophrenia.&lt;h4>Method&lt;/h4>We recruited patients with schizophrenia (n = 127), including patients at treatment initiation (n = 45), treatment-responsive patients (n = 40) and TR patients (n = 42), and healthy controls (n = 83). Clinical symptoms, neurocognitive function, and structural images were assessed. We performed group comparisons, and explored association of cortical thickness and cognition with TR.&lt;h4>Results&lt;/h4>The TR patients showed significantly more severe clinical symptoms and cognitive impairment relative to the t</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-26T07:45:42.698Z</modification><creation>2025-04-06T12:28:38.983Z</creation></dates><accession>S-EPMC9812867</accession><cross_references><pubmed>36184782</pubmed><doi>10.1111/pcn.13486</doi></cross_references></HashMap>