<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Amare AT</submitter><funding>BLRD VA</funding><funding>Intramural NIH HHS</funding><funding>NIDA NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>Department of Health | National Health and Medical Research Council (NHMRC)</funding><pagination>5251-5261</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11041653</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(12)</volume><pubmed_abstract>Lithium is regarded as the first-line treatment for bipolar disorder (BD), a severe and disabling mental health disorder that affects about 1% of the population worldwide. Nevertheless, lithium is not consistently effective, with only 30% of patients showing a favorable response to treatment. To provide personalized treatment options for bipolar patients, it is essential to identify prediction biomarkers such as polygenic scores. In this study, we developed a polygenic score for lithium treatment response (Li&lt;sup>+&lt;/sup>&lt;sub>PGS&lt;/sub>) in patients with BD. To gain further insights into lithium's possible molecular mechanism of action, we performed a genome-wide gene-based analysis. Using polygenic score modeling, via methods incorporating Bayesian regression and continuous shrinkage priors</pubmed_abstract><journal>Molecular psychiatry</journal><pubmed_title>Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder.</pubmed_title><pmcid>PMC11041653</pmcid><funding_grant_id>R01 MH059548</funding_grant_id><funding_grant_id>R01 MH059556</funding_grant_id><funding_grant_id>R01 MH059534</funding_grant_id><funding_grant_id>R01 MH059567</funding_grant_id><funding_grant_id>R01 MH059535</funding_grant_id><funding_grant_id>R01 MH059533</funding_grant_id><funding_grant_id>R01 MH060068</funding_grant_id><funding_grant_id>R01 MH059553</funding_grant_id><funding_grant_id>K02 DA021237</funding_grant_id><funding_grant_id>Emerging Leadership Investigator Grant 2021 - 2008000</funding_grant_id><funding_grant_id>ZIA MH002831</funding_grant_id><funding_grant_id>Z01 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T</pubmed_authors><pubmed_authors>Kalman JL</pubmed_authors><pubmed_authors>Haussleiter IS</pubmed_authors><pubmed_authors>Richard-Lepouriel H</pubmed_authors><pubmed_authors>Kircher T</pubmed_authors><pubmed_authors>Shimoda K</pubmed_authors><pubmed_authors>Arias B</pubmed_authors><pubmed_authors>Schmitt A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder.</name><description>Lithium is regarded as the first-line treatment for bipolar disorder (BD), a severe and disabling mental health disorder that affects about 1% of the population worldwide. Nevertheless, lithium is not consistently effective, with only 30% of patients showing a favorable response to treatment. To provide personalized treatment options for bipolar patients, it is essential to identify prediction biomarkers such as polygenic scores. In this study, we developed a polygenic score for lithium treatment response (Li&lt;sup>+&lt;/sup>&lt;sub>PGS&lt;/sub>) in patients with BD. To gain further insights into lithium's possible molecular mechanism of action, we performed a genome-wide gene-based analysis. Using polygenic score modeling, via methods incorporating Bayesian regression and continuous shrinkage priors</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2026-07-15T08:19:01.711Z</modification><creation>2026-07-01T03:12:28.494Z</creation></dates><accession>S-EPMC11041653</accession><cross_references><pubmed>37433967</pubmed><doi>10.1038/s41380-023-02149-1</doi></cross_references></HashMap>