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Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning

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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429672/
https://www.ncbi.nlm.nih.gov/pubmed/34127797
http://dx.doi.org/10.1038/s41386-021-01051-0
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author 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.
author_facet 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.
author_sort Pelin, Helena
collection PubMed
description 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.
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spelling pubmed-84296722021-09-24 Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning 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. Neuropsychopharmacology Article 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. Springer International Publishing 2021-06-14 2021-10 /pmc/articles/PMC8429672/ /pubmed/34127797 http://dx.doi.org/10.1038/s41386-021-01051-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
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.
Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning
title Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning
title_full Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning
title_fullStr Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning
title_full_unstemmed Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning
title_short Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning
title_sort identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429672/
https://www.ncbi.nlm.nih.gov/pubmed/34127797
http://dx.doi.org/10.1038/s41386-021-01051-0
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