Dopamine-Induced Dysconnectivity Between Salience Network and Auditory Cortex in Subjects With Psychotic-like Experiences: A Randomized Double-Blind Placebo-Controlled Study
Dopamine is involved in the pathophysiology of schizophrenia. Disrupted salience processing by the salience network (SN) may be a central link between dysregulated dopamine function and psychotic symptoms. However, dopaminergic influence on the SN and its presumed influence on psychotic and subpsych...
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Published in | Schizophrenia bulletin Vol. 46; no. 3; pp. 732 - 740 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Oxford University Press
10.04.2020
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Online Access | Get full text |
ISSN | 0586-7614 1745-1701 1745-1701 |
DOI | 10.1093/schbul/sbz110 |
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Abstract | Dopamine is involved in the pathophysiology of schizophrenia. Disrupted salience processing by the salience network (SN) may be a central link between dysregulated dopamine function and psychotic symptoms. However, dopaminergic influence on the SN and its presumed influence on psychotic and subpsychotic symptoms or psychotic-like experiences in healthy individuals remain unclear. Therefore, we investigated dopamine-induced changes in functional connectivity of the right anterior insula (rAI), a central SN hub, and their association with psychotic-like experiences. We enrolled 54 healthy, right-handed male subjects in a randomized, double-blind, cross-sectional placebo-controlled experiment. Psychotic-like experiences were assessed using the revised Exceptional Experiences Questionnaire (PAGE-R). They then received either placebo (n = 32) or 200 mg L-DOPA (n = 33), a dopamine precursor, orally and underwent resting-state functional magnetic resonance imaging. In a seed-to-voxel approach, we analyzed dopamine-induced changes in functional connectivity of the rAI and assessed the relationship between functional connectivity changes and PAGE-R score. L-DOPA reduced functional connectivity between the rAI and the left auditory cortex planum polare. In the placebo group, we found a strong negative correlation between PAGE-R score and rAI to planum polare functional connectivity; in the L-DOPA group, there was a strong positive correlation between PAGE-R score and functional connectivity between rAI and planum polare. The PAGE-R score explained about 30% of the functional connectivity variation between rAI and planum polare in the two groups. Our findings suggest that psychotic-like experiences are associated with dopamine-induced disruption of auditory input to the SN, which may lead to aberrant attribution of salience. |
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AbstractList | Dopamine is involved in the pathophysiology of schizophrenia. Disrupted salience processing by the salience network (SN) may be a central link between dysregulated dopamine function and psychotic symptoms. However, dopaminergic influence on the SN and its presumed influence on psychotic and subpsychotic symptoms or psychotic-like experiences in healthy individuals remain unclear. Therefore, we investigated dopamine-induced changes in functional connectivity of the right anterior insula (rAI), a central SN hub, and their association with psychotic-like experiences. We enrolled 54 healthy, right-handed male subjects in a randomized, double-blind, cross-sectional placebo-controlled experiment. Psychotic-like experiences were assessed using the revised Exceptional Experiences Questionnaire (PAGE-R). They then received either placebo (n = 32) or 200 mg L-DOPA (n = 33), a dopamine precursor, orally and underwent resting-state functional magnetic resonance imaging. In a seed-to-voxel approach, we analyzed dopamine-induced changes in functional connectivity of the rAI and assessed the relationship between functional connectivity changes and PAGE-R score. L-DOPA reduced functional connectivity between the rAI and the left auditory cortex planum polare. In the placebo group, we found a strong negative correlation between PAGE-R score and rAI to planum polare functional connectivity; in the L-DOPA group, there was a strong positive correlation between PAGE-R score and functional connectivity between rAI and planum polare. The PAGE-R score explained about 30% of the functional connectivity variation between rAI and planum polare in the two groups. Our findings suggest that psychotic-like experiences are associated with dopamine-induced disruption of auditory input to the SN, which may lead to aberrant attribution of salience.Dopamine is involved in the pathophysiology of schizophrenia. Disrupted salience processing by the salience network (SN) may be a central link between dysregulated dopamine function and psychotic symptoms. However, dopaminergic influence on the SN and its presumed influence on psychotic and subpsychotic symptoms or psychotic-like experiences in healthy individuals remain unclear. Therefore, we investigated dopamine-induced changes in functional connectivity of the right anterior insula (rAI), a central SN hub, and their association with psychotic-like experiences. We enrolled 54 healthy, right-handed male subjects in a randomized, double-blind, cross-sectional placebo-controlled experiment. Psychotic-like experiences were assessed using the revised Exceptional Experiences Questionnaire (PAGE-R). They then received either placebo (n = 32) or 200 mg L-DOPA (n = 33), a dopamine precursor, orally and underwent resting-state functional magnetic resonance imaging. In a seed-to-voxel approach, we analyzed dopamine-induced changes in functional connectivity of the rAI and assessed the relationship between functional connectivity changes and PAGE-R score. L-DOPA reduced functional connectivity between the rAI and the left auditory cortex planum polare. In the placebo group, we found a strong negative correlation between PAGE-R score and rAI to planum polare functional connectivity; in the L-DOPA group, there was a strong positive correlation between PAGE-R score and functional connectivity between rAI and planum polare. The PAGE-R score explained about 30% of the functional connectivity variation between rAI and planum polare in the two groups. Our findings suggest that psychotic-like experiences are associated with dopamine-induced disruption of auditory input to the SN, which may lead to aberrant attribution of salience. Dopamine is involved in the pathophysiology of schizophrenia. Disrupted salience processing by the salience network (SN) may be a central link between dysregulated dopamine function and psychotic symptoms. However, dopaminergic influence on the SN and its presumed influence on psychotic and subpsychotic symptoms or psychotic-like experiences in healthy individuals remain unclear. Therefore, we investigated dopamine-induced changes in functional connectivity of the right anterior insula (rAI), a central SN hub, and their association with psychotic-like experiences. We enrolled 54 healthy, right-handed male subjects in a randomized, double-blind, cross-sectional placebo-controlled experiment. Psychotic-like experiences were assessed using the revised Exceptional Experiences Questionnaire (PAGE-R). They then received either placebo (n = 32) or 200 mg L-DOPA (n = 33), a dopamine precursor, orally and underwent resting-state functional magnetic resonance imaging. In a seed-to-voxel approach, we analyzed dopamine-induced changes in functional connectivity of the rAI and assessed the relationship between functional connectivity changes and PAGE-R score. L-DOPA reduced functional connectivity between the rAI and the left auditory cortex planum polare. In the placebo group, we found a strong negative correlation between PAGE-R score and rAI to planum polare functional connectivity; in the L-DOPA group, there was a strong positive correlation between PAGE-R score and functional connectivity between rAI and planum polare. The PAGE-R score explained about 30% of the functional connectivity variation between rAI and planum polare in the two groups. Our findings suggest that psychotic-like experiences are associated with dopamine-induced disruption of auditory input to the SN, which may lead to aberrant attribution of salience. Dopamine is involved in the pathophysiology of schizophrenia. Disrupted salience processing by the salience network (SN) may be a central link between dysregulated dopamine function and psychotic symptoms. However, dopaminergic influence on the SN and its presumed influence on psychotic and subpsychotic symptoms or psychotic-like experiences in healthy individuals remain unclear. Therefore, we investigated dopamine-induced changes in functional connectivity of the right anterior insula (rAI), a central SN hub, and their association with psychotic-like experiences. We enrolled 54 healthy, right-handed male subjects in a randomized, double-blind, cross-sectional placebo-controlled experiment. Psychotic-like experiences were assessed using the revised Exceptional Experiences Questionnaire (PAGE-R). They then received either placebo ( n = 32) or 200 mg L-DOPA ( n = 33), a dopamine precursor, orally and underwent resting-state functional magnetic resonance imaging. In a seed-to-voxel approach, we analyzed dopamine-induced changes in functional connectivity of the rAI and assessed the relationship between functional connectivity changes and PAGE-R score. L-DOPA reduced functional connectivity between the rAI and the left auditory cortex planum polare. In the placebo group, we found a strong negative correlation between PAGE-R score and rAI to planum polare functional connectivity; in the L-DOPA group, there was a strong positive correlation between PAGE-R score and functional connectivity between rAI and planum polare. The PAGE-R score explained about 30% of the functional connectivity variation between rAI and planum polare in the two groups. Our findings suggest that psychotic-like experiences are associated with dopamine-induced disruption of auditory input to the SN, which may lead to aberrant attribution of salience. |
Author | Seifritz, Erich Rössler, Wulf Wyss, Thomas Rössler, Julian Wotruba, Diana Unterrassner, Lui Haker, Helene |
AuthorAffiliation | 1 Collegium Helveticum, University of Zurich and ETH Zurich , Zurich, Switzerland 4 Laboratory of Neuroscience (LIM 27), Institute of Psychiatry, University of Sao Paulo , Sao Paulo, Brazil 6 Translational Neuromodeling Unit (TNU), Institute for Biomedical Engineering, University of Zurich and ETH Zurich , Zurich, Switzerland 7 The Zurich Program for Sustainable Development of Mental Health Services (ZInEP), University Hospital of Psychiatry Zurich , Zurich, Switzerland 2 Institute of Anesthesiology, University Hospital Zurich , Zurich, Switzerland 3 Department of Psychiatry, Psychotherapy and Psychosomatics, University of Zurich , Zurich, Switzerland 5 Department of Psychiatry and Psychotherapy, Charité Mitte , Charité, Berlin, Germany |
AuthorAffiliation_xml | – name: 3 Department of Psychiatry, Psychotherapy and Psychosomatics, University of Zurich , Zurich, Switzerland – name: 4 Laboratory of Neuroscience (LIM 27), Institute of Psychiatry, University of Sao Paulo , Sao Paulo, Brazil – name: 5 Department of Psychiatry and Psychotherapy, Charité Mitte , Charité, Berlin, Germany – name: 2 Institute of Anesthesiology, University Hospital Zurich , Zurich, Switzerland – name: 6 Translational Neuromodeling Unit (TNU), Institute for Biomedical Engineering, University of Zurich and ETH Zurich , Zurich, Switzerland – name: 1 Collegium Helveticum, University of Zurich and ETH Zurich , Zurich, Switzerland – name: 7 The Zurich Program for Sustainable Development of Mental Health Services (ZInEP), University Hospital of Psychiatry Zurich , Zurich, Switzerland |
Author_xml | – sequence: 1 givenname: Julian orcidid: 0000-0002-7601-6493 surname: Rössler fullname: Rössler, Julian email: julian.roessler@usz.ch organization: Collegium Helveticum, University of Zurich and ETH Zurich, Zurich, Switzerland – sequence: 2 givenname: Wulf surname: Rössler fullname: Rössler, Wulf organization: Collegium Helveticum, University of Zurich and ETH Zurich, Zurich, Switzerland – sequence: 3 givenname: Erich surname: Seifritz fullname: Seifritz, Erich organization: Department of Psychiatry, Psychotherapy and Psychosomatics, University of Zurich, Zurich, Switzerland – sequence: 4 givenname: Lui surname: Unterrassner fullname: Unterrassner, Lui organization: Collegium Helveticum, University of Zurich and ETH Zurich, Zurich, Switzerland – sequence: 5 givenname: Thomas surname: Wyss fullname: Wyss, Thomas organization: Collegium Helveticum, University of Zurich and ETH Zurich, Zurich, Switzerland – sequence: 6 givenname: Helene surname: Haker fullname: Haker, Helene organization: Department of Psychiatry, Psychotherapy and Psychosomatics, University of Zurich, Zurich, Switzerland – sequence: 7 givenname: Diana surname: Wotruba fullname: Wotruba, Diana organization: Collegium Helveticum, University of Zurich and ETH Zurich, Zurich, Switzerland |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31751466$$D View this record in MEDLINE/PubMed |
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Keywords | resting-state functional magnetic resonance imaging exceptional experiences salience planum polare functional connectivity L-DOPA |
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SubjectTerms | Adult Auditory Cortex - diagnostic imaging Auditory Cortex - drug effects Auditory Cortex - metabolism Auditory Cortex - physiopathology Auditory Perception - physiology Connectome Cross-Sectional Studies Dopamine Dopamine - metabolism Dopamine Agents - administration & dosage Dopamine Agents - pharmacology Double-Blind Method Humans Levodopa - administration & dosage Levodopa - pharmacology Magnetic Resonance Imaging Male Nerve Net - diagnostic imaging Nerve Net - drug effects Nerve Net - metabolism Nerve Net - physiopathology Psychosis Psychotic Disorders - diagnostic imaging Psychotic Disorders - metabolism Psychotic Disorders - physiopathology Regular Young Adult |
Title | Dopamine-Induced Dysconnectivity Between Salience Network and Auditory Cortex in Subjects With Psychotic-like Experiences: A Randomized Double-Blind Placebo-Controlled Study |
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