Association of Polygenic Score and the involvement of Cholinergic and Glutamatergic Pathways with Lithium Treatment Response in Patients with Bipolar Disorder.
Journal
Research square
Titre abrégé: Res Sq
Pays: United States
ID NLM: 101768035
Informations de publication
Date de publication:
14 Feb 2023
14 Feb 2023
Historique:
entrez:
24
2
2023
pubmed:
25
2
2023
medline:
25
2
2023
Statut:
epublish
Résumé
Lithium is regarded as the first-line treatment for bipolar disorder (BD), a severe and disabling mental 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+PGS) 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, Li+PGS was developed in the International Consortium of Lithium Genetics cohort (ConLi+Gen: N=2,367) and replicated in the combined PsyCourse (N=89) and BipoLife (N=102) studies. The associations of Li+PGS and lithium treatment response - defined in a continuous ALDA scale and a categorical outcome (good response vs. poor response) were tested using regression models, each adjusted for the covariates: age, sex, and the first four genetic principal components. Statistical significance was determined at P<����������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������.
Identifiants
pubmed: 36824922
doi: 10.21203/rs.3.rs-2580252/v1
pmc: PMC9949170
pii:
doi:
Types de publication
Preprint
Langues
eng
Subventions
Organisme : NIMH NIH HHS
ID : R01 MH059556
Pays : United States
Organisme : Intramural NIH HHS
ID : Z01 MH002810
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH059535
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH059567
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH059545
Pays : United States
Organisme : NCI NIH HHS
ID : P01 CA089392
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH059548
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH059534
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH059533
Pays : United States
Organisme : NIDA NIH HHS
ID : K02 DA021237
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH059553
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH060068
Pays : United States
Commentaires et corrections
Type : UpdateIn
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