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Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning

Authors :
Axel Krug
Susanne Meinert
Helena Pelin
Markus M. Nöthen
Tilo Kircher
Julia Pfarr
Bertram Müller-Myhsok
Simon Schmitt
Marcus Ising
Ramona Leenings
Jonathan Repple
Igor Nenadic
Marcella Rietschel
Lena Waltemate
Tina Meller
Alexandra Winter
Stephanie H. Witt
Kai Ringwald
Katharina Brosch
Stefanie Heilmann-Heimbach
Andreas J. Forstner
Till F. M. Andlauer
Tim Hahn
Fabian Streit
Nils Opel
Katharina Thiel
Nils R. Winter
Udo Dannlowski
Hannah Lemke
Frederike Stein
Source :
Neuropsychopharmacology 46(11), 1895-1905 (2021). doi:10.1038/s41386-021-01051-0
Publication Year :
2021
Publisher :
Nature Publishing Group, 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
Database :
OpenAIRE
Journal :
Neuropsychopharmacology 46(11), 1895-1905 (2021). doi:10.1038/s41386-021-01051-0
Accession number :
edsair.doi.dedup.....6a90bf481dc9671305384c420468f47d
Full Text :
https://doi.org/10.1038/s41386-021-01051-0