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A preliminary transcriptomic analysis of the orbitofrontal cortex of antisocial individuals
AIMS: Antisocial personality disorder (ASPD) and conduct disorder (CD) are characterized by a persistent pattern of violations of societal norms and others' rights. Ample evidence shows that the pathophysiology of these disorders is contributed by orbitofrontal cortex (OFC) alterations, yet the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580340/ https://www.ncbi.nlm.nih.gov/pubmed/37269073 http://dx.doi.org/10.1111/cns.14283 |
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author | Piras, Ignazio S. Braccagni, Giulia Huentelman, Matthew J. Bortolato, Marco |
author_facet | Piras, Ignazio S. Braccagni, Giulia Huentelman, Matthew J. Bortolato, Marco |
author_sort | Piras, Ignazio S. |
collection | PubMed |
description | AIMS: Antisocial personality disorder (ASPD) and conduct disorder (CD) are characterized by a persistent pattern of violations of societal norms and others' rights. Ample evidence shows that the pathophysiology of these disorders is contributed by orbitofrontal cortex (OFC) alterations, yet the underlying molecular mechanisms remain elusive. To address this knowledge gap, we performed the first‐ever RNA sequencing study of postmortem OFC samples from subjects with a lifetime diagnosis of ASPD and/or CD. METHODS: The transcriptomic profiles of OFC samples from subjects with ASPD and/or CD were compared to those of unaffected age‐matched controls (n = 9/group). RESULTS: The OFC of ASPD/CD‐affected subjects displayed significant differences in the expression of 328 genes. Further gene‐ontology analyses revealed an extensive downregulation of excitatory neuron transcripts and upregulation of astrocyte transcripts. These alterations were paralleled by significant modifications in synaptic regulation and glutamatergic neurotransmission pathways. CONCLUSION: These preliminary findings suggest that ASPD and CD feature a complex array of functional deficits in the pyramidal neurons and astrocytes of the OFC. In turn, these aberrances may contribute to the reduced OFC connectivity observed in antisocial subjects. Future analyses on larger cohorts are needed to validate these results. |
format | Online Article Text |
id | pubmed-10580340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105803402023-10-18 A preliminary transcriptomic analysis of the orbitofrontal cortex of antisocial individuals Piras, Ignazio S. Braccagni, Giulia Huentelman, Matthew J. Bortolato, Marco CNS Neurosci Ther Original Articles AIMS: Antisocial personality disorder (ASPD) and conduct disorder (CD) are characterized by a persistent pattern of violations of societal norms and others' rights. Ample evidence shows that the pathophysiology of these disorders is contributed by orbitofrontal cortex (OFC) alterations, yet the underlying molecular mechanisms remain elusive. To address this knowledge gap, we performed the first‐ever RNA sequencing study of postmortem OFC samples from subjects with a lifetime diagnosis of ASPD and/or CD. METHODS: The transcriptomic profiles of OFC samples from subjects with ASPD and/or CD were compared to those of unaffected age‐matched controls (n = 9/group). RESULTS: The OFC of ASPD/CD‐affected subjects displayed significant differences in the expression of 328 genes. Further gene‐ontology analyses revealed an extensive downregulation of excitatory neuron transcripts and upregulation of astrocyte transcripts. These alterations were paralleled by significant modifications in synaptic regulation and glutamatergic neurotransmission pathways. CONCLUSION: These preliminary findings suggest that ASPD and CD feature a complex array of functional deficits in the pyramidal neurons and astrocytes of the OFC. In turn, these aberrances may contribute to the reduced OFC connectivity observed in antisocial subjects. Future analyses on larger cohorts are needed to validate these results. John Wiley and Sons Inc. 2023-06-02 /pmc/articles/PMC10580340/ /pubmed/37269073 http://dx.doi.org/10.1111/cns.14283 Text en © 2023 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Piras, Ignazio S. Braccagni, Giulia Huentelman, Matthew J. Bortolato, Marco A preliminary transcriptomic analysis of the orbitofrontal cortex of antisocial individuals |
title | A preliminary transcriptomic analysis of the orbitofrontal cortex of antisocial individuals |
title_full | A preliminary transcriptomic analysis of the orbitofrontal cortex of antisocial individuals |
title_fullStr | A preliminary transcriptomic analysis of the orbitofrontal cortex of antisocial individuals |
title_full_unstemmed | A preliminary transcriptomic analysis of the orbitofrontal cortex of antisocial individuals |
title_short | A preliminary transcriptomic analysis of the orbitofrontal cortex of antisocial individuals |
title_sort | preliminary transcriptomic analysis of the orbitofrontal cortex of antisocial individuals |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580340/ https://www.ncbi.nlm.nih.gov/pubmed/37269073 http://dx.doi.org/10.1111/cns.14283 |
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