Martin, Andrew K., Mowry, B. (2016) Increased rare duplication burden genomewide in patients with treatment-resistant schizophrenia. Psychological Medicine, 46 (3). pp. 469-476. ISSN 0033-2917. (doi:10.1017/S0033291715001701) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:79707)
The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided. | |
Official URL: https://doi.org/10.1017/S0033291715001701 |
Abstract
Background A significant number of patients with schizophrenia fail to respond to antipsychotic medication. Although several studies have investigated associated patient characteristics, the emerging findings from genetic studies offer further scope for study. Method In 612 schizophrenia patients with detailed clinical information, common genetic variants indexed by polygenic risk scores, and rare variants indexed by deletion and duplication burden genomewide, we explored potential genetic predictors alongside other established risk factors for treatment resistance. Clinical outcomes of treatment resistance were also calculated using lifetime measures of positive, negative/disorganized and mood symptoms as well as number of hospitalizations and suicide attempts. Results Logistic regression models identified a significant relationship between treatment resistance and total duplication burden genomewide, years of formal schooling and age at onset. Clinically, treatment-resistant patients were characterized by greater negative/disorganized and positive symptoms and greater number of hospitalizations. Conclusions Taken together, these findings suggest genetic information, specifically the genomewide burden of rare copy number variants, may increase our understanding and clinical management of patients with treatment-resistant schizophrenia.
Item Type: | Article |
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DOI/Identification number: | 10.1017/S0033291715001701 |
Uncontrolled keywords: | clozapine; neuroleptic agent, adolescent; adult; Australia; cohort analysis; copy number variation; drug resistance; female; genetics; hospitalization; human; male; multifactorial inheritance; onset age; risk factor; schizophrenia; statistical model; statistics and numerical data; suicide attempt; treatment failure; young adult, Adolescent; Adult; Age of Onset; Antipsychotic Agents; Australia; Clozapine; Cohort Studies; DNA Copy Number Variations; Drug Resistance; Female; Hospitalization; Humans; Logistic Models; Male; Multifactorial Inheritance; Risk Factors; Schizophrenia; Suicide, Attempted; Treatment Failure; Young Adult |
Divisions: | Divisions > Division of Human and Social Sciences > School of Psychology |
Depositing User: | Andrew Martin |
Date Deposited: | 05 Feb 2020 10:04 UTC |
Last Modified: | 05 Nov 2024 12:44 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/79707 (The current URI for this page, for reference purposes) |
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