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Lack of cortico-limbic coupling in bipolar disorder and schizophrenia during emotion regulation
Bipolar disorder (BD) and schizophrenia (Sz) share dysfunction in prefrontal inhibitory brain systems, yet exhibit distinct forms of affective disturbance. We aimed to distinguish these disorders on the basis of differential activation in cortico-limbic pathways during voluntary emotion regulation....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3309531/ https://www.ncbi.nlm.nih.gov/pubmed/22832855 http://dx.doi.org/10.1038/tp.2012.16 |
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author | Morris, R W Sparks, A Mitchell, P B Weickert, C S Green, M J |
author_facet | Morris, R W Sparks, A Mitchell, P B Weickert, C S Green, M J |
author_sort | Morris, R W |
collection | PubMed |
description | Bipolar disorder (BD) and schizophrenia (Sz) share dysfunction in prefrontal inhibitory brain systems, yet exhibit distinct forms of affective disturbance. We aimed to distinguish these disorders on the basis of differential activation in cortico-limbic pathways during voluntary emotion regulation. Patients with DSM-IV diagnosed Sz (12) or BD-I (13) and 15 healthy control (HC) participants performed a well-established emotion regulation task while undergoing functional magnetic resonance imaging. The task required participants to voluntarily upregulate or downregulate their subjective affect while viewing emotionally negative images or maintain their affective response as a comparison condition. In BD, abnormal overactivity (hyperactivation) occurred in the right ventrolateral prefrontal cortex (VLPFC) during up- and downregulation of negative affect, relative to HC. Among Sz, prefrontal hypoactivation of the right VLPFC occurred during downregulation (opposite to BD), whereas upregulation elicited hyperactivity in the right VLPFC similar to BD. Amygdala activity was significantly related to subjective negative affect in HC and BD, but not Sz. Furthermore, amygdala activity was inversely coupled with the activity in the left PFC during downregulation in HC (r=−0.76), while such coupling did not occur in BD or Sz. These preliminary results indicate that differential cortico-limbic activation can distinguish the clinical groups in line with affective disturbance: BD is characterized by ineffective cortical control over limbic regions during emotion regulation, while Sz is characterized by an apparent failure to engage cortical (hypofrontality) and limbic regions during downregulation. |
format | Online Article Text |
id | pubmed-3309531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-33095312012-04-03 Lack of cortico-limbic coupling in bipolar disorder and schizophrenia during emotion regulation Morris, R W Sparks, A Mitchell, P B Weickert, C S Green, M J Transl Psychiatry Original Article Bipolar disorder (BD) and schizophrenia (Sz) share dysfunction in prefrontal inhibitory brain systems, yet exhibit distinct forms of affective disturbance. We aimed to distinguish these disorders on the basis of differential activation in cortico-limbic pathways during voluntary emotion regulation. Patients with DSM-IV diagnosed Sz (12) or BD-I (13) and 15 healthy control (HC) participants performed a well-established emotion regulation task while undergoing functional magnetic resonance imaging. The task required participants to voluntarily upregulate or downregulate their subjective affect while viewing emotionally negative images or maintain their affective response as a comparison condition. In BD, abnormal overactivity (hyperactivation) occurred in the right ventrolateral prefrontal cortex (VLPFC) during up- and downregulation of negative affect, relative to HC. Among Sz, prefrontal hypoactivation of the right VLPFC occurred during downregulation (opposite to BD), whereas upregulation elicited hyperactivity in the right VLPFC similar to BD. Amygdala activity was significantly related to subjective negative affect in HC and BD, but not Sz. Furthermore, amygdala activity was inversely coupled with the activity in the left PFC during downregulation in HC (r=−0.76), while such coupling did not occur in BD or Sz. These preliminary results indicate that differential cortico-limbic activation can distinguish the clinical groups in line with affective disturbance: BD is characterized by ineffective cortical control over limbic regions during emotion regulation, while Sz is characterized by an apparent failure to engage cortical (hypofrontality) and limbic regions during downregulation. Nature Publishing Group 2012-03 2012-03-13 /pmc/articles/PMC3309531/ /pubmed/22832855 http://dx.doi.org/10.1038/tp.2012.16 Text en Copyright © 2012 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Morris, R W Sparks, A Mitchell, P B Weickert, C S Green, M J Lack of cortico-limbic coupling in bipolar disorder and schizophrenia during emotion regulation |
title | Lack of cortico-limbic coupling in bipolar disorder and schizophrenia during emotion regulation |
title_full | Lack of cortico-limbic coupling in bipolar disorder and schizophrenia during emotion regulation |
title_fullStr | Lack of cortico-limbic coupling in bipolar disorder and schizophrenia during emotion regulation |
title_full_unstemmed | Lack of cortico-limbic coupling in bipolar disorder and schizophrenia during emotion regulation |
title_short | Lack of cortico-limbic coupling in bipolar disorder and schizophrenia during emotion regulation |
title_sort | lack of cortico-limbic coupling in bipolar disorder and schizophrenia during emotion regulation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3309531/ https://www.ncbi.nlm.nih.gov/pubmed/22832855 http://dx.doi.org/10.1038/tp.2012.16 |
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