Multi‐polygenic scores in psychiatry: From disorder specific to transdiagnostic perspectives

Author:

Shi Yingjie12ORCID,Sprooten Emma123,Mulders Peter24,Vrijsen Janna245,Bralten Janita12,Demontis Ditte678,Børglum Anders D.678,Walters G. Bragi910ORCID,Stefansson Kari910,van Eijndhoven Philip24,Tendolkar Indira24,Franke Barbara124,Mota Nina Roth12

Affiliation:

1. Department of Human Genetics Radboud University Medical Center Nijmegen The Netherlands

2. Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen The Netherlands

3. Department of Cognitive Neuroscience Radboud University Medical Center Nijmegen The Netherlands

4. Department of Psychiatry Radboud University Medical Center Nijmegen The Netherlands

5. Pro Persona Mental Health Care Depression Expertise Centre Nijmegen The Netherlands

6. Department of Biomedicine/Human Genetics Aarhus University Aarhus Denmark

7. The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH Copenhagen Denmark

8. Center for Genomics and Personalized Medicine Aarhus Denmark

9. deCODE Genetics Reykjavík Iceland

10. Faculty of Medicine University of Iceland Reykjavík Iceland

Abstract

AbstractThe dense co‐occurrence of psychiatric disorders questions the categorical classification tradition and motivates efforts to establish dimensional constructs with neurobiological foundations that transcend diagnostic boundaries. In this study, we examined the genetic liability for eight major psychiatric disorder phenotypes under both a disorder‐specific and a transdiagnostic framework. The study sample (n = 513) was deeply phenotyped, consisting of 452 patients from tertiary care with mood disorders, anxiety disorders (ANX), attention‐deficit/hyperactivity disorder (ADHD), autism spectrum disorders, and/or substance use disorders (SUD) and 61 unaffected comparison individuals. We computed subject‐specific polygenic risk score (PRS) profiles and assessed their associations with psychiatric diagnoses, comorbidity status, as well as cross‐disorder behavioral dimensions derived from a rich battery of psychopathology assessments. High PRSs for depression were unselectively associated with the diagnosis of SUD, ADHD, ANX, and mood disorders (p < 1e‐4). In the dimensional approach, four distinct functional domains were uncovered, namely the negative valence, social, cognitive, and regulatory systems, closely matching the major functional domains proposed by the Research Domain Criteria (RDoC) framework. Critically, the genetic predisposition for depression was selectively reflected in the functional aspect of negative valence systems (R2 = 0.041, p = 5e‐4) but not others. This study adds evidence to the ongoing discussion about the misalignment between current psychiatric nosology and the underlying psychiatric genetic etiology and underscores the effectiveness of the dimensional approach in both the functional characterization of psychiatric patients and the delineation of the genetic liability for psychiatric disorders.

Funder

Radboud Universitair Medisch Centrum

Brain and Behavior Research Foundation

Novo Nordisk Fonden

Lundbeck Foundation

National Institute of Mental Health

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

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