» Articles » PMID: 36824922

Association of Polygenic Score and the Involvement of Cholinergic and Glutamatergic Pathways with Lithium Treatment Response in Patients with Bipolar Disorder

Overview
Journal Res Sq
Date 2023 Feb 24
PMID 36824922
Authors
Affiliations
Soon will be listed here.
Abstract

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<����������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������.

References
1.
Niswender C, Conn P . Metabotropic glutamate receptors: physiology, pharmacology, and disease. Annu Rev Pharmacol Toxicol. 2010; 50:295-322. PMC: 2904507. DOI: 10.1146/annurev.pharmtox.011008.145533. View

2.
Le Clerc S, Lombardi L, Baune B, Amare A, Schubert K, Hou L . HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders. Sci Rep. 2021; 11(1):17823. PMC: 8426488. DOI: 10.1038/s41598-021-97140-7. View

3.
Schubert K, Thalamuthu A, Amare A, Frank J, Streit F, Adl M . Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients. Transl Psychiatry. 2021; 11(1):606. PMC: 8630000. DOI: 10.1038/s41398-021-01702-2. View

4.
Manchia M, Adli M, Akula N, Ardau R, Aubry J, Backlund L . Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report. PLoS One. 2013; 8(6):e65636. PMC: 3686769. DOI: 10.1371/journal.pone.0065636. View

5.
Mercier M, Lodge D . Group III metabotropic glutamate receptors: pharmacology, physiology and therapeutic potential. Neurochem Res. 2014; 39(10):1876-94. DOI: 10.1007/s11064-014-1415-y. View