<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Perlis RH</submitter><funding>NIMH NIH HHS</funding><pagination>2810-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10034848</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(12)</volume><pubmed_abstract>Recent rodent models of antidepressant response implicate a novel set of genes in mechanisms of antidepressant action. The authors examined variants in four such genes (KCNK2 (TREK1), SLC18A2 (VMAT2), S100A10, and HDAC5) for association with remission in a large effectiveness trial of antidepressant treatments. Subjects were drawn from the Sequenced Treatment Alternatives to Relieve Depression (STAR(*)D) study, a multicenter, prospective, effectiveness trial in major depressive disorder (MDD). Outpatients with nonpsychotic MDD were initially treated with citalopram for up to 14 weeks; those who did not remit with citalopram were sequentially randomized to a series of next-step treatments, each for up to 12 weeks. Single-nucleotide polymorphisms in four genes were examined for association w</pubmed_abstract><journal>Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology</journal><pubmed_title>Pharmacogenetic analysis of genes implicated in rodent models of antidepressant response: association of TREK1 and treatment resistance in the STAR(*)D study.</pubmed_title><pmcid>PMC10034848</pmcid><funding_grant_id>N01 MH090003</funding_grant_id><funding_grant_id>K23 MH067060</funding_grant_id><pubmed_authors>Fava M</pubmed_authors><pubmed_authors>Trivedi MH</pubmed_authors><pubmed_authors>Fagerness J</pubmed_authors><pubmed_authors>Purcell S</pubmed_authors><pubmed_authors>Perlis RH</pubmed_authors><pubmed_authors>Rush AJ</pubmed_authors><pubmed_authors>Smoller JW</pubmed_authors><pubmed_authors>Moorjani P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pharmacogenetic analysis of genes implicated in rodent models of antidepressant response: association of TREK1 and treatment resistance in the STAR(*)D study.</name><description>Recent rodent models of antidepressant response implicate a novel set of genes in mechanisms of antidepressant action. The authors examined variants in four such genes (KCNK2 (TREK1), SLC18A2 (VMAT2), S100A10, and HDAC5) for association with remission in a large effectiveness trial of antidepressant treatments. Subjects were drawn from the Sequenced Treatment Alternatives to Relieve Depression (STAR(*)D) study, a multicenter, prospective, effectiveness trial in major depressive disorder (MDD). Outpatients with nonpsychotic MDD were initially treated with citalopram for up to 14 weeks; those who did not remit with citalopram were sequentially randomized to a series of next-step treatments, each for up to 12 weeks. Single-nucleotide polymorphisms in four genes were examined for association w</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Nov</publication><modification>2026-05-29T07:52:12.091Z</modification><creation>2025-07-24T03:03:58.325Z</creation></dates><accession>S-EPMC10034848</accession><cross_references><pubmed>18288090</pubmed><doi>10.1038/npp.2008.6</doi></cross_references></HashMap>