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Synaptic and brain-expressed gene sets relate to the shared genetic risk across five psychiatric disorders
BACKGROUND: Mounting evidence shows genetic overlap between multiple psychiatric disorders. However, the biological underpinnings of shared risk for psychiatric disorders are not yet fully uncovered. The identification of underlying biological mechanisms is crucial for the progress in the treatment...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408577/ https://www.ncbi.nlm.nih.gov/pubmed/31328717 http://dx.doi.org/10.1017/S0033291719001776 |
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author | Hammerschlag, Anke R. de Leeuw, Christiaan A. Middeldorp, Christel M. Polderman, Tinca J. C. |
author_facet | Hammerschlag, Anke R. de Leeuw, Christiaan A. Middeldorp, Christel M. Polderman, Tinca J. C. |
author_sort | Hammerschlag, Anke R. |
collection | PubMed |
description | BACKGROUND: Mounting evidence shows genetic overlap between multiple psychiatric disorders. However, the biological underpinnings of shared risk for psychiatric disorders are not yet fully uncovered. The identification of underlying biological mechanisms is crucial for the progress in the treatment of these disorders. METHODS: We applied gene-set analysis including 7372 gene sets, and 53 tissue-type specific gene-expression profiles to identify sets of genes that are involved in the etiology of multiple psychiatric disorders. We included genome-wide meta-association data of the five psychiatric disorders schizophrenia, bipolar disorder, major depressive disorder, autism spectrum disorder, and attention-deficit/hyperactivity disorder. The total dataset contained 159 219 cases and 262 481 controls. RESULTS: We identified 19 gene sets that were significantly associated with the five psychiatric disorders combined, of which we excluded five sets because their associations were likely driven by schizophrenia only. Conditional analyses showed independent effects of several gene sets that in particular relate to the synapse. In addition, we found independent effects of gene expression levels in the cerebellum and frontal cortex. CONCLUSIONS: We obtained novel evidence for shared biological mechanisms that act across psychiatric disorders and we showed that several gene sets that have been related to individual disorders play a role in a broader range of psychiatric disorders. |
format | Online Article Text |
id | pubmed-7408577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-74085772020-08-19 Synaptic and brain-expressed gene sets relate to the shared genetic risk across five psychiatric disorders Hammerschlag, Anke R. de Leeuw, Christiaan A. Middeldorp, Christel M. Polderman, Tinca J. C. Psychol Med Original Articles BACKGROUND: Mounting evidence shows genetic overlap between multiple psychiatric disorders. However, the biological underpinnings of shared risk for psychiatric disorders are not yet fully uncovered. The identification of underlying biological mechanisms is crucial for the progress in the treatment of these disorders. METHODS: We applied gene-set analysis including 7372 gene sets, and 53 tissue-type specific gene-expression profiles to identify sets of genes that are involved in the etiology of multiple psychiatric disorders. We included genome-wide meta-association data of the five psychiatric disorders schizophrenia, bipolar disorder, major depressive disorder, autism spectrum disorder, and attention-deficit/hyperactivity disorder. The total dataset contained 159 219 cases and 262 481 controls. RESULTS: We identified 19 gene sets that were significantly associated with the five psychiatric disorders combined, of which we excluded five sets because their associations were likely driven by schizophrenia only. Conditional analyses showed independent effects of several gene sets that in particular relate to the synapse. In addition, we found independent effects of gene expression levels in the cerebellum and frontal cortex. CONCLUSIONS: We obtained novel evidence for shared biological mechanisms that act across psychiatric disorders and we showed that several gene sets that have been related to individual disorders play a role in a broader range of psychiatric disorders. Cambridge University Press 2020-07 2019-07-22 /pmc/articles/PMC7408577/ /pubmed/31328717 http://dx.doi.org/10.1017/S0033291719001776 Text en © Cambridge University Press 2019 http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Hammerschlag, Anke R. de Leeuw, Christiaan A. Middeldorp, Christel M. Polderman, Tinca J. C. Synaptic and brain-expressed gene sets relate to the shared genetic risk across five psychiatric disorders |
title | Synaptic and brain-expressed gene sets relate to the shared genetic risk across five psychiatric disorders |
title_full | Synaptic and brain-expressed gene sets relate to the shared genetic risk across five psychiatric disorders |
title_fullStr | Synaptic and brain-expressed gene sets relate to the shared genetic risk across five psychiatric disorders |
title_full_unstemmed | Synaptic and brain-expressed gene sets relate to the shared genetic risk across five psychiatric disorders |
title_short | Synaptic and brain-expressed gene sets relate to the shared genetic risk across five psychiatric disorders |
title_sort | synaptic and brain-expressed gene sets relate to the shared genetic risk across five psychiatric disorders |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408577/ https://www.ncbi.nlm.nih.gov/pubmed/31328717 http://dx.doi.org/10.1017/S0033291719001776 |
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