Association Between Polygenic Risk Scores and Outcome of ECT.
Bipolar and Related Disorders
Depressive Disorders
Electroconvulsive Therapy (ECT)
Genetics/Genomics
Journal
The American journal of psychiatry
ISSN: 1535-7228
Titre abrégé: Am J Psychiatry
Pays: United States
ID NLM: 0370512
Informations de publication
Date de publication:
01 11 2022
01 11 2022
Historique:
pubmed:
8
9
2022
medline:
3
11
2022
entrez:
7
9
2022
Statut:
ppublish
Résumé
Identifying biomarkers associated with response to electroconvulsive therapy (ECT) may aid clinical decisions. The authors examined whether greater polygenic liabilities for major depressive disorder, bipolar disorder, and schizophrenia are associated with improvement following ECT for a major depressive episode. Between 2013 and 2017, patients who had at least one treatment series recorded in the Swedish National Quality Register for ECT were invited to provide a blood sample for genotyping. The present study included 2,320 participants (median age, 51 years; 62.8% women) who had received an ECT series for a major depressive episode (77.1% unipolar depression), who had a registered treatment outcome, and whose polygenic risk scores (PRSs) could be calculated. Ordinal logistic regression was used to estimate the effect of PRS on Clinical Global Impressions improvement scale (CGI-I) score after each ECT series. Greater PRS for major depressive disorder was significantly associated with less improvement on the CGI-I (odds ratio per standard deviation, 0.89, 95% CI=0.82, 0.96; R Improvement after ECT is associated with polygenic liability for major depressive disorder and bipolar disorder, providing evidence of a genetic component for ECT clinical response. These liabilities may be considered along with clinical predictors in future prediction models of ECT outcomes.
Identifiants
pubmed: 36069021
doi: 10.1176/appi.ajp.22010045
pmc: PMC10113810
mid: NIHMS1887447
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
844-852Subventions
Organisme : NIMH NIH HHS
ID : R01 MH121545
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH123724
Pays : United States
Commentaires et corrections
Type : CommentIn
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