Abnormally increased effective connectivity between parahippocampal gyrus and ventromedial prefrontal regions during emotion labeling in bipolar disorder
Emotional liability and mood dysregulation characterize bipolar disorder (BD), yet no study has examined effective connectivity between parahippocampal gyrus and prefrontal cortical regions in ventromedial and dorsal/lateral neural systems subserving mood regulation in BD. Participants comprised 46...
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Published in | Psychiatry research. Neuroimaging Vol. 174; no. 3; pp. 195 - 201 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Ireland Ltd
30.12.2009
Elsevier |
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Abstract | Emotional liability and mood dysregulation characterize bipolar disorder (BD), yet no study has examined effective connectivity between parahippocampal gyrus and prefrontal cortical regions in ventromedial and dorsal/lateral neural systems subserving mood regulation in BD. Participants comprised 46 individuals (age range: 18–56 years): 21 with a DSM-IV diagnosis of BD, type I currently remitted; and 25 age- and gender-matched healthy controls (HC). Participants performed an event-related functional magnetic resonance imaging paradigm, viewing mild and intense happy and neutral faces. We employed dynamic causal modeling (DCM) to identify significant alterations in effective connectivity between BD and HC. Bayes model selection was used to determine the best model. The right parahippocampal gyrus (PHG) and right subgenual cingulate gyrus (sgCG) were included as representative regions of the ventromedial neural system. The right dorsolateral prefrontal cortex (DLPFC) region was included as representative of the dorsal/lateral neural system. Right PHG–sgCG effective connectivity was significantly greater in BD than HC, reflecting more rapid, forward PHG–sgCG signaling in BD than HC. There was no between-group difference in sgCG–DLPFC effective connectivity. In BD, abnormally increased right PHG–sgCG effective connectivity and reduced right PHG activity to emotional stimuli suggest a dysfunctional ventromedial neural system implicated in early stimulus appraisal, encoding and automatic regulation of emotion that may represent a pathophysiological functional neural mechanism for mood dysregulation in BD. |
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AbstractList | Abstract Emotional liability and mood dysregulation characterize bipolar disorder (BD), yet no study has examined effective connectivity between parahippocampal gyrus and prefrontal cortical regions in ventromedial and dorsal/lateral neural systems subserving mood regulation in BD. Participants comprised 46 individuals (age range: 18–56 years): 21 with a DSM-IV diagnosis of BD, type I currently remitted; and 25 age- and gender-matched healthy controls (HC). Participants performed an event-related functional magnetic resonance imaging paradigm, viewing mild and intense happy and neutral faces. We employed dynamic causal modeling (DCM) to identify significant alterations in effective connectivity between BD and HC. Bayes model selection was used to determine the best model. The right parahippocampal gyrus (PHG) and right subgenual cingulate gyrus (sgCG) were included as representative regions of the ventromedial neural system. The right dorsolateral prefrontal cortex (DLPFC) region was included as representative of the dorsal/lateral neural system. Right PHG–sgCG effective connectivity was significantly greater in BD than HC, reflecting more rapid, forward PHG–sgCG signaling in BD than HC. There was no between-group difference in sgCG–DLPFC effective connectivity. In BD, abnormally increased right PHG–sgCG effective connectivity and reduced right PHG activity to emotional stimuli suggest a dysfunctional ventromedial neural system implicated in early stimulus appraisal, encoding and automatic regulation of emotion that may represent a pathophysiological functional neural mechanism for mood dysregulation in BD. Emotional liability and mood dysregulation characterize bipolar disorder (BD), yet no study has examined effective connectivity between parahippocampal gyrus and prefrontal cortical regions in ventromedial and dorsal/lateral neural systems subserving mood regulation in BD. Participants comprised 46 individuals (age range: 18-56 years): 21 with a DSM-IV diagnosis of BD, type I currently remitted; and 25 age- and gender-matched healthy controls (HC). Participants performed an event-related functional magnetic resonance imaging paradigm, viewing mild and intense happy and neutral faces. We employed dynamic causal modeling (DCM) to identify significant alterations in effective connectivity between BD and HC. Bayes model selection was used to determine the best model. The right parahippocampal gyrus (PHG) and right subgenual cingulate gyrus (sgCG) were included as representative regions of the ventromedial neural system. The right dorsolateral prefrontal cortex (DLPFC) region was included as representative of the dorsal/lateral neural system. Right PHG-sgCG effective connectivity was significantly greater in BD than HC, reflecting more rapid, forward PHG-sgCG signaling in BD than HC. There was no between-group difference in sgCG-DLPFC effective connectivity. In BD, abnormally increased right PHG-sgCG effective connectivity and reduced right PHG activity to emotional stimuli suggest a dysfunctional ventromedial neural system implicated in early stimulus appraisal, encoding and automatic regulation of emotion that may represent a pathophysiological functional neural mechanism for mood dysregulation in BD. Emotional liability and mood dysregulation characterize bipolar disorder (BD), yet no study has examined effective connectivity between parahippocampal gyrus and prefrontal cortical regions in ventromedial and dorsal/lateral neural systems subserving mood regulation in BD. Participants comprised 46 individuals (age range: 18-56 years): 21 with a DSM-IV diagnosis of BD, type I currently remitted; and 25 age- and gender-matched healthy controls (HC). Participants performed an event-related functional magnetic resonance imaging paradigm, viewing mild and intense happy and neutral faces. We employed dynamic causal modeling (DCM) to identify significant alterations in effective connectivity between BD and HC. Bayes model selection was used to determine the best model. The right parahippocampal gyrus (PHG) and right subgenual cingulate gyrus (sgCG) were included as representative regions of the ventromedial neural system. The right dorsolateral prefrontal cortex (DLPFC) region was included as representative of the dorsal/lateral neural system. Right PHG-sgCG effective connectivity was significantly greater in BD than HC, reflecting more rapid, forward PHG-sgCG signaling in BD than HC. There was no between-group difference in sgCG-DLPFC effective connectivity. In BD, abnormally increased right PHG-sgCG effective connectivity and reduced right PHG activity to emotional stimuli suggest a dysfunctional ventromedial neural system implicated in early stimulus appraisal, encoding and automatic regulation of emotion that may represent a pathophysiological functional neural mechanism for mood dysregulation in BD.Emotional liability and mood dysregulation characterize bipolar disorder (BD), yet no study has examined effective connectivity between parahippocampal gyrus and prefrontal cortical regions in ventromedial and dorsal/lateral neural systems subserving mood regulation in BD. Participants comprised 46 individuals (age range: 18-56 years): 21 with a DSM-IV diagnosis of BD, type I currently remitted; and 25 age- and gender-matched healthy controls (HC). Participants performed an event-related functional magnetic resonance imaging paradigm, viewing mild and intense happy and neutral faces. We employed dynamic causal modeling (DCM) to identify significant alterations in effective connectivity between BD and HC. Bayes model selection was used to determine the best model. The right parahippocampal gyrus (PHG) and right subgenual cingulate gyrus (sgCG) were included as representative regions of the ventromedial neural system. The right dorsolateral prefrontal cortex (DLPFC) region was included as representative of the dorsal/lateral neural system. Right PHG-sgCG effective connectivity was significantly greater in BD than HC, reflecting more rapid, forward PHG-sgCG signaling in BD than HC. There was no between-group difference in sgCG-DLPFC effective connectivity. In BD, abnormally increased right PHG-sgCG effective connectivity and reduced right PHG activity to emotional stimuli suggest a dysfunctional ventromedial neural system implicated in early stimulus appraisal, encoding and automatic regulation of emotion that may represent a pathophysiological functional neural mechanism for mood dysregulation in BD. Emotional liability and mood dysregulation characterize bipolar disorder (BD), yet no study has examined effective connectivity between parahippocampal gyrus and prefrontal cortical regions in ventromedial and dorsal/lateral neural systems subserving mood regulation in BD. Forty-six individuals (age range: 18–56 years); 21 with a DSM-IV diagnosis of BD, type I currently remitted; 25 age- and gender-matched healthy controls (HC). Participants performed an event-related paradigm, viewing mild and intense happy and neutral faces. We employed dynamic causal modeling (DCM) to identify significant alterations in effective connectivity between BD and HC. Bayes model selection was used to determine the best model. The right parahippocampal gyrus (PHG) and right subgenual cingulate gyrus (sgCG) were included as representative regions of the ventromedial neural system. The right dorsolateral prefrontal cortex (DLPFC) region was included as representative of the dorsal/lateral neural system. Right PHG-sgCG effective connectivity was significantly greater in BD than HC, reflecting more rapid, forward PHG-sgCG signaling in BD than HC. There was no between-group difference in sgCG-DLPFC effective connectivity. In BD, abnormally increased right PHG-sgCG effective connectivity and reduced right PHG activity to emotional stimuli suggest a dysfunctional ventromedial neural system implicated in early stimulus appraisal, encoding and automatic regulation of emotion, that may represent a pathophysiological functional neural mechanism for mood dysregulation in BD. |
Author | Hassel, Stefanie Kupfer, David J. Versace, Amelia Phillips, Mary L. Mechelli, Andrea Almeida, Jorge R.C. |
AuthorAffiliation | c Department of Psychology, Institute of Psychiatry, United Kingdom d Department of Psychological Medicine, Cardiff University School of Medicine, United Kingdom a Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA b Department of Psychiatry, University of São Paulo Medical School, São Paulo, Brazil |
AuthorAffiliation_xml | – name: b Department of Psychiatry, University of São Paulo Medical School, São Paulo, Brazil – name: a Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA – name: d Department of Psychological Medicine, Cardiff University School of Medicine, United Kingdom – name: c Department of Psychology, Institute of Psychiatry, United Kingdom |
Author_xml | – sequence: 1 givenname: Jorge R.C. surname: Almeida fullname: Almeida, Jorge R.C. organization: Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA – sequence: 2 givenname: Andrea surname: Mechelli fullname: Mechelli, Andrea organization: Department of Psychology, Institute of Psychiatry, London, United Kingdom – sequence: 3 givenname: Stefanie surname: Hassel fullname: Hassel, Stefanie organization: Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA – sequence: 4 givenname: Amelia surname: Versace fullname: Versace, Amelia organization: Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA – sequence: 5 givenname: David J. surname: Kupfer fullname: Kupfer, David J. organization: Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA – sequence: 6 givenname: Mary L. surname: Phillips fullname: Phillips, Mary L. email: phillipsml@upmc.edu organization: Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA |
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Keywords | Neuroimaging fMRI Bipolar disorder Dynamic causal modeling Emotion regulation Effective connectivity Mood disorder Human Affect affectivity Central nervous system ParahIppocampal cortex Labelling Emotion emotionality Prefrontal cortex Nuclear magnetic resonance imaging Encephalon Medical imagery Self regulation Causality Functional imaging |
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Snippet | Emotional liability and mood dysregulation characterize bipolar disorder (BD), yet no study has examined effective connectivity between parahippocampal gyrus... Abstract Emotional liability and mood dysregulation characterize bipolar disorder (BD), yet no study has examined effective connectivity between... |
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SubjectTerms | Adult Adult and adolescent clinical studies Bayes Theorem Biological and medical sciences Bipolar disorder Bipolar Disorder - pathology Bipolar Disorder - physiopathology Bipolar disorders Brain Mapping Case-Control Studies Dynamic causal modeling Effective connectivity Emotion regulation Emotions - physiology Female fMRI Humans Image Processing, Computer-Assisted Magnetic Resonance Imaging Male Medical sciences Models, Statistical Mood disorders Neural Pathways Neuroimaging Neuropsychological Tests Nonlinear Dynamics Oxygen Parahippocampal Gyrus - blood supply Parahippocampal Gyrus - physiopathology Prefrontal Cortex - blood supply Prefrontal Cortex - physiopathology Psychiatry Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Radiology Young Adult |
Title | Abnormally increased effective connectivity between parahippocampal gyrus and ventromedial prefrontal regions during emotion labeling in bipolar disorder |
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