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Brain transcriptomic profiling reveals common alterations across neurodegenerative and psychiatric disorders
Neurodegenerative and neuropsychiatric disorders (ND-NPs) are multifactorial, polygenic and complex behavioral phenotypes caused by brain abnormalities. Large-scale collaborative efforts have tried to identify the genetic architecture of these conditions. However, the specific and shared underlying...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research Network of Computational and Structural Biotechnology
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428860/ https://www.ncbi.nlm.nih.gov/pubmed/36090817 http://dx.doi.org/10.1016/j.csbj.2022.08.037 |
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author | Sadeghi, Iman Gispert, Juan D. Palumbo, Emilio Muñoz-Aguirre, Manuel Wucher, Valentin D'Argenio, Valeria Santpere, Gabriel Navarro, Arcadi Guigo, Roderic Vilor-Tejedor, Natàlia |
author_facet | Sadeghi, Iman Gispert, Juan D. Palumbo, Emilio Muñoz-Aguirre, Manuel Wucher, Valentin D'Argenio, Valeria Santpere, Gabriel Navarro, Arcadi Guigo, Roderic Vilor-Tejedor, Natàlia |
author_sort | Sadeghi, Iman |
collection | PubMed |
description | Neurodegenerative and neuropsychiatric disorders (ND-NPs) are multifactorial, polygenic and complex behavioral phenotypes caused by brain abnormalities. Large-scale collaborative efforts have tried to identify the genetic architecture of these conditions. However, the specific and shared underlying molecular pathobiology of brain illnesses is not clear. Here, we examine transcriptome-wide characterization of eight conditions, using a total of 2,633 post-mortem brain samples from patients with Alzheimer’s disease (AD), Parkinson’s disease (PD), Progressive Supranuclear Palsy (PSP), Pathological Aging (PA), Autism Spectrum Disorder (ASD), Schizophrenia (Scz), Major Depressive Disorder (MDD), and Bipolar Disorder (BP)–in comparison with 2,078 brain samples from matched control subjects. Similar transcriptome alterations were observed between NDs and NPs with the top correlations obtained between Scz-BP, ASD-PD, AD-PD, and Scz-ASD. Region-specific comparisons also revealed shared transcriptome alterations in frontal and temporal lobes across NPs and NDs. Co-expression network analysis identified coordinated dysregulations of cell-type-specific modules across NDs and NPs. This study provides a transcriptomic framework to understand the molecular alterations of NPs and NDs through their shared- and specific gene expression in the brain. |
format | Online Article Text |
id | pubmed-9428860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Research Network of Computational and Structural Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-94288602022-09-09 Brain transcriptomic profiling reveals common alterations across neurodegenerative and psychiatric disorders Sadeghi, Iman Gispert, Juan D. Palumbo, Emilio Muñoz-Aguirre, Manuel Wucher, Valentin D'Argenio, Valeria Santpere, Gabriel Navarro, Arcadi Guigo, Roderic Vilor-Tejedor, Natàlia Comput Struct Biotechnol J Research Article Neurodegenerative and neuropsychiatric disorders (ND-NPs) are multifactorial, polygenic and complex behavioral phenotypes caused by brain abnormalities. Large-scale collaborative efforts have tried to identify the genetic architecture of these conditions. However, the specific and shared underlying molecular pathobiology of brain illnesses is not clear. Here, we examine transcriptome-wide characterization of eight conditions, using a total of 2,633 post-mortem brain samples from patients with Alzheimer’s disease (AD), Parkinson’s disease (PD), Progressive Supranuclear Palsy (PSP), Pathological Aging (PA), Autism Spectrum Disorder (ASD), Schizophrenia (Scz), Major Depressive Disorder (MDD), and Bipolar Disorder (BP)–in comparison with 2,078 brain samples from matched control subjects. Similar transcriptome alterations were observed between NDs and NPs with the top correlations obtained between Scz-BP, ASD-PD, AD-PD, and Scz-ASD. Region-specific comparisons also revealed shared transcriptome alterations in frontal and temporal lobes across NPs and NDs. Co-expression network analysis identified coordinated dysregulations of cell-type-specific modules across NDs and NPs. This study provides a transcriptomic framework to understand the molecular alterations of NPs and NDs through their shared- and specific gene expression in the brain. Research Network of Computational and Structural Biotechnology 2022-08-19 /pmc/articles/PMC9428860/ /pubmed/36090817 http://dx.doi.org/10.1016/j.csbj.2022.08.037 Text en © 2022 Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Sadeghi, Iman Gispert, Juan D. Palumbo, Emilio Muñoz-Aguirre, Manuel Wucher, Valentin D'Argenio, Valeria Santpere, Gabriel Navarro, Arcadi Guigo, Roderic Vilor-Tejedor, Natàlia Brain transcriptomic profiling reveals common alterations across neurodegenerative and psychiatric disorders |
title | Brain transcriptomic profiling reveals common alterations across neurodegenerative and psychiatric disorders |
title_full | Brain transcriptomic profiling reveals common alterations across neurodegenerative and psychiatric disorders |
title_fullStr | Brain transcriptomic profiling reveals common alterations across neurodegenerative and psychiatric disorders |
title_full_unstemmed | Brain transcriptomic profiling reveals common alterations across neurodegenerative and psychiatric disorders |
title_short | Brain transcriptomic profiling reveals common alterations across neurodegenerative and psychiatric disorders |
title_sort | brain transcriptomic profiling reveals common alterations across neurodegenerative and psychiatric disorders |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428860/ https://www.ncbi.nlm.nih.gov/pubmed/36090817 http://dx.doi.org/10.1016/j.csbj.2022.08.037 |
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