<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang T</submitter><funding>Jiangsu Provincial Key Research and Development Program</funding><funding>National Natural Science Foundation of China</funding><pagination>264-274</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10924577</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>69(4)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>This study established a machine learning model based on the multidimensional data of resting-state functional activity of the brain and &lt;i>P11&lt;/i> gene DNA methylation to predict the early efficacy of antidepressant treatment in patients with major depressive disorder (MDD).&lt;h4>Methods&lt;/h4>A total of 98 Han Chinese MDD were analysed in this study. Patients were divided into 51 responders and 47 nonresponders according to whether the Hamilton Depression Rating Scale-17 items (HAMD-17) reduction rate was ≥50% after 2 weeks of antidepressant treatment. At baseline, the Illumina HiSeq Platform was used to detect the methylation of 74 CpG sites of the &lt;i>P11&lt;/i> gene in peripheral blood samples. Resting-state functional magnetic resonance imaging (rs-fMRI) scan detected the a</pubmed_abstract><journal>Canadian journal of psychiatry. Revue canadienne de psychiatrie</journal><pubmed_title>Prediction of Early Antidepressant Efficacy in Patients with Major Depressive Disorder Based on Multidimensional Features of rs-fMRI and &amp;lt;i&amp;gt;P11&amp;lt;/i&amp;gt; Gene DNA Methylation: Prediction de l'efficacite precoce d'un antidepresseur chez des patients souffrant du trouble depressif majeur d'apres les caracteristiques multidimensionnelles de la methylation de l'ADN du gene P11 et de la IRMf-rs.</pubmed_title><pmcid>PMC10924577</pmcid><funding_grant_id>BE2019748</funding_grant_id><funding_grant_id>81901375</funding_grant_id><funding_grant_id>82271570</funding_grant_id><funding_grant_id>81971277</funding_grant_id><pubmed_authors>Yin Y</pubmed_authors><pubmed_authors>Hou Z</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Gao C</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Jiang W</pubmed_authors><pubmed_authors>Wang T</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Kong Y</pubmed_authors><pubmed_authors>Yue Y</pubmed_authors><pubmed_authors>Xu Z</pubmed_authors><pubmed_authors>Yuan Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prediction of Early Antidepressant Efficacy in Patients with Major Depressive Disorder Based on Multidimensional Features of rs-fMRI and &amp;lt;i&amp;gt;P11&amp;lt;/i&amp;gt; Gene DNA Methylation: Prediction de l'efficacite precoce d'un antidepresseur chez des patients souffrant du trouble depressif majeur d'apres les caracteristiques multidimensionnelles de la methylation de l'ADN du gene P11 et de la IRMf-rs.</name><description>&lt;h4>Objective&lt;/h4>This study established a machine learning model based on the multidimensional data of resting-state functional activity of the brain and &lt;i>P11&lt;/i> gene DNA methylation to predict the early efficacy of antidepressant treatment in patients with major depressive disorder (MDD).&lt;h4>Methods&lt;/h4>A total of 98 Han Chinese MDD were analysed in this study. Patients were divided into 51 responders and 47 nonresponders according to whether the Hamilton Depression Rating Scale-17 items (HAMD-17) reduction rate was ≥50% after 2 weeks of antidepressant treatment. At baseline, the Illumina HiSeq Platform was used to detect the methylation of 74 CpG sites of the &lt;i>P11&lt;/i> gene in peripheral blood samples. Resting-state functional magnetic resonance imaging (rs-fMRI) scan detected the a</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2025-04-04T18:53:41.738Z</modification><creation>2025-04-04T18:53:41.738Z</creation></dates><accession>S-EPMC10924577</accession><cross_references><pubmed>37920958</pubmed><doi>10.1177/07067437231210787</doi></cross_references></HashMap>