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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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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. |
format | Online Article Text |
id | pubmed-8429672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
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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