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Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning

Authors :
Pelin, Helena
Ising, Marcus
Stein, Frederike
Meinert, Susanne
Meller, Tina
Brosch, Katharina
Winter, Nils R.
Krug, Axel
Leenings, Ramona
Lemke, Hannah
Nenadić, Igor
Heilmann-Heimbach, Stefanie
Forstner, Andreas J.
Nöthen, Markus M.
Opel, Nils
Repple, Jonathan
Pfarr, Julia
Ringwald, Kai
Schmitt, Simon
Thiel, Katharina
Waltemate, Lena
Winter, Alexandra
Streit, Fabian
Witt, Stephanie
Rietschel, Marcella
Dannlowski, Udo
Kircher, Tilo
Hahn, Tim
Müller-Myhsok, Bertram
Andlauer, Till F. M.
Source :
Neuropsychopharmacology; October 2021, Vol. 46 Issue: 11 p1895-1905, 11p
Publication Year :
2021

Abstract

Psychiatric disorders show heterogeneous symptoms and trajectories, with current nosology not accurately reflecting their molecular etiology and the variability and symptomatic overlap within and between diagnostic classes. This heterogeneity impedes timely and targeted treatment. Our study aimed to identify psychiatric patient clusters that share clinical and genetic features and may profit from similar therapies. We used high-dimensional data clustering on deep clinical data to identify transdiagnostic groups in a discovery sample (N= 1250) of healthy controls and patients diagnosed with depression, bipolar disorder, schizophrenia, schizoaffective disorder, and other psychiatric disorders. We observed five diagnostically mixed clusters and ordered them based on severity. The least impaired cluster 0, containing most healthy controls, showed general well-being. Clusters 1–3 differed predominantly regarding levels of maltreatment, depression, daily functioning, and parental bonding. Cluster 4 contained most patients diagnosed with psychotic disorders and exhibited the highest severity in many dimensions, including medication load. Depressed patients were present in all clusters, indicating that we captured different disease stages or subtypes. We replicated all but the smallest cluster 1 in an independent sample (N= 622). Next, we analyzed genetic differences between clusters using polygenic scores (PGS) and the psychiatric family history. These genetic variables differed mainly between clusters 0 and 4 (prediction area under the receiver operating characteristic curve (AUC) = 81%; significant PGS: cross-disorder psychiatric risk, schizophrenia, and educational attainment). Our results confirm that psychiatric disorders consist of heterogeneous subtypes sharing molecular factors and symptoms. The identification of transdiagnostic clusters advances our understanding of the heterogeneity of psychiatric disorders and may support the development of personalized treatments.

Details

Language :
English
ISSN :
0893133X and 1740634X
Volume :
46
Issue :
11
Database :
Supplemental Index
Journal :
Neuropsychopharmacology
Publication Type :
Periodical
Accession number :
ejs56800238
Full Text :
https://doi.org/10.1038/s41386-021-01051-0