Psychopathological Syndromes Across Affective and Psychotic Disorders Correlate With Gray Matter Volumes

Author:

Stein Frederike12,Meller Tina12ORCID,Brosch Katharina12,Schmitt Simon12,Ringwald Kai12,Pfarr Julia Katharina12,Meinert Susanne3,Thiel Katharina3,Lemke Hannah3,Waltemate Lena3ORCID,Grotegerd Dominik3,Opel Nils3,Jansen Andreas12,Nenadić Igor12ORCID,Dannlowski Udo3,Krug Axel124,Kircher Tilo12ORCID

Affiliation:

1. Department of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany

2. Center for Mind Brain and Behavior, University of Marburg, Marburg, Germany

3. Department of Psychiatry University of Münster, Münster, Germany

4. Department of Psychiatry and Psychotherapy, University of Bonn, Bonn, Germany

Abstract

Abstract Introduction More than a century of research on the neurobiological underpinnings of major psychiatric disorders (major depressive disorder [MDD], bipolar disorder [BD], schizophrenia [SZ], and schizoaffective disorder [SZA]) has been unable to identify diagnostic markers. An alternative approach is to study dimensional psychopathological syndromes that cut across categorical diagnoses. The aim of the current study was to identify gray matter volume (GMV) correlates of transdiagnostic symptom dimensions. Methods We tested the association of 5 psychopathological factors with GMV using multiple regression models in a sample of N = 1069 patients meeting Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) criteria for MDD (n = 818), BD (n = 132), and SZ/SZA (n = 119). T1-weighted brain images were acquired with 3-Tesla magnetic resonance imaging and preprocessed with CAT12. Interactions analyses (diagnosis × psychopathological factor) were performed to test whether local GMV associations were driven by DSM-IV diagnosis. We further tested syndrome specific regions of interest (ROIs). Results Whole brain analysis showed a significant negative association of the positive formal thought disorder factor with GMV in the right middle frontal gyrus, the paranoid-hallucinatory syndrome in the right fusiform, and the left middle frontal gyri. ROI analyses further showed additional negative associations, including the negative syndrome with bilateral frontal opercula, positive formal thought disorder with the left amygdala-hippocampus complex, and the paranoid-hallucinatory syndrome with the left angular gyrus. None of the GMV associations interacted with DSM-IV diagnosis. Conclusions We found associations between psychopathological syndromes and regional GMV independent of diagnosis. Our findings open a new avenue for neurobiological research across disorders, using syndrome-based approaches rather than categorical diagnoses.

Funder

UKGM

Forschungscampus Mittelhessen

German Research Foundation

Research Unit FOR2107

Publisher

Oxford University Press (OUP)

Subject

Psychiatry and Mental health

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