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GWAS Study

Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders.

David FS, Stein F, Andlauer TFM et al.

36652833 PubMed ID
GWAS Study Type
1858 Participants
69 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DF
David FS
SF
Stein F
AT
Andlauer TFM
SF
Streit F
WS
Witt SH
HS
Herms S
HP
Hoffmann P
HS
Heilmann-Heimbach S
ON
Opel N
RJ
Repple J
JA
Jansen A
NI
Nenadić I
PS
Papiol S
HU
Heilbronner U
KJ
Kalman JL
SS
Schaupp SK
SF
Senner F
SE
Schulte EC
FP
Falkai PG
ST
Schulze TG
DU
Dannlowski U
KT
Kircher T
RM
Rietschel M
NM
Nöthen MM
KA
Krug A
FA
Forstner AJ
Chapter II

Abstract

Summary of the research findings

Major depressive disorder (MDD), bipolar disorder (BD), and schizophrenia spectrum disorders (SZ) exhibit considerable phenotypic and genetic overlap. However, the contribution of genetic factors to their shared psychopathological symptom dimensions remains unclear. The present exploratory study investigated genetic contributions to the symptom dimensions "Depression", "Negative syndrome", "Positive formal thought disorder", "Paranoid-hallucinatory syndrome", and "Increased appetite" in a transdiagnostic subset of the German FOR2107 cohort (n = 1042 patients with MDD, BD, or SZ). As replication cohort, a subset of the German/Austrian PsyCourse study (n = 816 patients with MDD, BD, or SZ) was employed. First, the relationship between symptom dimensions and common variants associated with MDD, BD, and SZ was investigated via polygenic risk score (PRS) association analyses, with disorder-specific PRS as predictors and symptom dimensions as outcomes. In the FOR2107 study sample, PRS for BD and SZ were positively associated with "Positive formal thought disorder", the PRS for SZ was positively associated with "Paranoid-hallucinatory syndrome", and the PRS for BD was negatively associated with "Depression". The effects of PRS for SZ were replicated in PsyCourse. No significant associations were observed for the MDD PRS. Second, genome-wide association studies (GWAS) were performed for the five symptom dimensions. No genome-wide significant associations and no replicable suggestive associations (p < 1e-6 in the GWAS) were identified. In summary, our results suggest that, similar to diagnostic categories, transdiagnostic psychiatric symptom dimensions are attributable to polygenic contributions with small effect sizes. Further studies in larger thoroughly phenotyped psychiatric cohorts are required to elucidate the genetic factors that shape psychopathological symptom dimensions.

1,042 individuals

Chapter III

Study Statistics

Key metrics and study information

1858
Total Participants
GWAS
Study Type
Yes
Replicated
816 individuals
Replication Participants
Chapter IV

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