Altered Autonomic Function in Individuals at Clinical High Risk for Psychosis
Alterations in autonomic functioning in individuals diagnosed with schizophrenia are well-documented. Yet, it is currently unclear whether these dysfunctions extend into the clinical high-risk state. Thus, we investigated resting heart rate (RHR) and heart rate variability (HRV) indices in individua...
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Published in | Frontiers in psychiatry Vol. 11; p. 580503 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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06.11.2020
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Abstract | Alterations in autonomic functioning in individuals diagnosed with schizophrenia are well-documented. Yet, it is currently unclear whether these dysfunctions extend into the clinical high-risk state. Thus, we investigated resting heart rate (RHR) and heart rate variability (HRV) indices in individuals at clinical high-risk for psychosis (CHR-P).
We recruited 117 CHR-P participants, 38 participants with affective disorders and substance abuse (CHR-N) as well as a group of 49 healthy controls. CHR-P status was assessed with the Comprehensive Assessment of At-Risk Mental States (CAARMS) and the Schizophrenia Proneness Instrument, Adult Version (SPI-A). We obtained 5 min, eyes-open resting-state MEG data, which was used for the extraction of cardiac field-related inter-beat-interval data and from which heart-rate and heart-rate variability measures were computed.
Compared to both CHR-N and healthy controls, CHR-P participants were characterized by an increased RHR, which was not explained by differences in psychopathological comorbidity and medication status. Increased RHR correlated with the presence of subthreshold psychotic symptoms and associated distress. No differences between groups were found for heart-rate variability measures, however. Furthermore, there was an association between motor-performance and psychophysiological measures.
The current study provides evidence of alterations in autonomic functioning as disclosed by increased RHR in CHR-P participants. Future studies are needed to further evaluate this characteristic feature of CHR-P individuals and its potential predictive value for psychosis development. |
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AbstractList | Alterations in autonomic functioning in individuals diagnosed with schizophrenia are well-documented. Yet, it is currently unclear whether these dysfunctions extend into the clinical high-risk state. Thus, we investigated resting heart rate (RHR) and heart rate variability (HRV) indices in individuals at clinical high-risk for psychosis (CHR-P).
We recruited 117 CHR-P participants, 38 participants with affective disorders and substance abuse (CHR-N) as well as a group of 49 healthy controls. CHR-P status was assessed with the Comprehensive Assessment of At-Risk Mental States (CAARMS) and the Schizophrenia Proneness Instrument, Adult Version (SPI-A). We obtained 5 min, eyes-open resting-state MEG data, which was used for the extraction of cardiac field-related inter-beat-interval data and from which heart-rate and heart-rate variability measures were computed.
Compared to both CHR-N and healthy controls, CHR-P participants were characterized by an increased RHR, which was not explained by differences in psychopathological comorbidity and medication status. Increased RHR correlated with the presence of subthreshold psychotic symptoms and associated distress. No differences between groups were found for heart-rate variability measures, however. Furthermore, there was an association between motor-performance and psychophysiological measures.
The current study provides evidence of alterations in autonomic functioning as disclosed by increased RHR in CHR-P participants. Future studies are needed to further evaluate this characteristic feature of CHR-P individuals and its potential predictive value for psychosis development. Introduction: Alterations in autonomic functioning in individuals diagnosed with schizophrenia are well-documented. Yet, it is currently unclear whether these dysfunctions extend into the clinical high-risk state. Thus, we investigated resting heart rate (RHR) and heart rate variability (HRV) indices in individuals at clinical high-risk for psychosis (CHR-P).Methods: We recruited 117 CHR-P participants, 38 participants with affective disorders and substance abuse (CHR-N) as well as a group of 49 healthy controls. CHR-P status was assessed with the Comprehensive Assessment of At-Risk Mental States (CAARMS) and the Schizophrenia Proneness Instrument, Adult Version (SPI-A). We obtained 5 min, eyes-open resting-state MEG data, which was used for the extraction of cardiac field-related inter-beat-interval data and from which heart-rate and heart-rate variability measures were computed.Results: Compared to both CHR-N and healthy controls, CHR-P participants were characterized by an increased RHR, which was not explained by differences in psychopathological comorbidity and medication status. Increased RHR correlated with the presence of subthreshold psychotic symptoms and associated distress. No differences between groups were found for heart-rate variability measures, however. Furthermore, there was an association between motor-performance and psychophysiological measures.Conclusion: The current study provides evidence of alterations in autonomic functioning as disclosed by increased RHR in CHR-P participants. Future studies are needed to further evaluate this characteristic feature of CHR-P individuals and its potential predictive value for psychosis development. Introduction: Alterations in autonomic functioning in individuals diagnosed with schizophrenia are well-documented. Yet, it is currently unclear whether these dysfunctions extend into the clinical high-risk state. Thus, we investigated resting heart rate (RHR) and heart rate variability (HRV) indices in individuals at clinical high-risk for psychosis (CHR-P). Methods: We recruited 117 CHR-P participants, 38 participants with affective disorders and substance abuse (CHR-N) as well as a group of 49 healthy controls. CHR-P status was assessed with the Comprehensive Assessment of At-Risk Mental States (CAARMS) and the Schizophrenia Proneness Instrument, Adult Version (SPI-A). We obtained 5 min, eyes-open resting-state MEG data, which was used for the extraction of cardiac field-related inter-beat-interval data and from which heart-rate and heart-rate variability measures were computed. Results: Compared to both CHR-N and healthy controls, CHR-P participants were characterized by an increased RHR, which was not explained by differences in psychopathological comorbidity and medication status. Increased RHR correlated with the presence of subthreshold psychotic symptoms and associated distress. No differences between groups were found for heart-rate variability measures, however. Furthermore, there was an association between motor-performance and psychophysiological measures. Conclusion: The current study provides evidence of alterations in autonomic functioning as disclosed by increased RHR in CHR-P participants. Future studies are needed to further evaluate this characteristic feature of CHR-P individuals and its potential predictive value for psychosis development. |
Author | Schultze-Lutter, Frauke Schwannauer, Matthias Gajwani, Ruchika Grent-'t-Jong, Tineke Uhlhaas, Peter J Gumley, Andrew I Lawrie, Stephen M Kocsis, Anna Gross, Joachim |
AuthorAffiliation | 3 Institute of Health and Wellbeing, University of Glasgow , Glasgow , United Kingdom 2 Department of Experimental Psychology, Ludwig-Maximilians-Universität München , Munich , Germany 5 Department of Clinical Psychology, University Edinburgh , Edinburgh , United Kingdom 4 Department of Psychiatry, University of Edinburgh , Edinburgh , United Kingdom 6 Department of Psychiatry and Psychotherapy, Medical Faculty, Heinrich-Heine University , Düsseldorf , Germany 7 Department of Psychology and Mental Health, Faculty of Psychology, Airlangga University , Surabaya , Indonesia 1 Institute for Neuroscience and Psychology, University of Glasgow , Glasgow , United Kingdom 8 Department of Child and Adolescent Psychiatry, Charité Universitätsmedizin , Berlin , Germany |
AuthorAffiliation_xml | – name: 7 Department of Psychology and Mental Health, Faculty of Psychology, Airlangga University , Surabaya , Indonesia – name: 8 Department of Child and Adolescent Psychiatry, Charité Universitätsmedizin , Berlin , Germany – name: 2 Department of Experimental Psychology, Ludwig-Maximilians-Universität München , Munich , Germany – name: 4 Department of Psychiatry, University of Edinburgh , Edinburgh , United Kingdom – name: 6 Department of Psychiatry and Psychotherapy, Medical Faculty, Heinrich-Heine University , Düsseldorf , Germany – name: 3 Institute of Health and Wellbeing, University of Glasgow , Glasgow , United Kingdom – name: 1 Institute for Neuroscience and Psychology, University of Glasgow , Glasgow , United Kingdom – name: 5 Department of Clinical Psychology, University Edinburgh , Edinburgh , United Kingdom |
Author_xml | – sequence: 1 givenname: Anna surname: Kocsis fullname: Kocsis, Anna organization: Department of Experimental Psychology, Ludwig-Maximilians-Universität München, Munich, Germany – sequence: 2 givenname: Ruchika surname: Gajwani fullname: Gajwani, Ruchika organization: Institute of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom – sequence: 3 givenname: Joachim surname: Gross fullname: Gross, Joachim organization: Institute for Neuroscience and Psychology, University of Glasgow, Glasgow, United Kingdom – sequence: 4 givenname: Andrew I surname: Gumley fullname: Gumley, Andrew I organization: Institute of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom – sequence: 5 givenname: Stephen M surname: Lawrie fullname: Lawrie, Stephen M organization: Department of Psychiatry, University of Edinburgh, Edinburgh, United Kingdom – sequence: 6 givenname: Matthias surname: Schwannauer fullname: Schwannauer, Matthias organization: Department of Clinical Psychology, University Edinburgh, Edinburgh, United Kingdom – sequence: 7 givenname: Frauke surname: Schultze-Lutter fullname: Schultze-Lutter, Frauke organization: Department of Psychology and Mental Health, Faculty of Psychology, Airlangga University, Surabaya, Indonesia – sequence: 8 givenname: Tineke surname: Grent-'t-Jong fullname: Grent-'t-Jong, Tineke organization: Department of Child and Adolescent Psychiatry, Charité Universitätsmedizin, Berlin, Germany – sequence: 9 givenname: Peter J surname: Uhlhaas fullname: Uhlhaas, Peter J organization: Department of Child and Adolescent Psychiatry, Charité Universitätsmedizin, Berlin, Germany |
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CitedBy_id | crossref_primary_10_3390_biomedicines12030523 crossref_primary_10_1186_s13023_024_03026_y crossref_primary_10_3389_fpsyt_2021_760396 crossref_primary_10_1016_j_schres_2023_03_012 |
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Copyright | Copyright © 2020 Kocsis, Gajwani, Gross, Gumley, Lawrie, Schwannauer, Schultze-Lutter, Grent-‘t-Jong and Uhlhaas. Copyright © 2020 Kocsis, Gajwani, Gross, Gumley, Lawrie, Schwannauer, Schultze-Lutter, Grent-‘t-Jong and Uhlhaas. 2020 Kocsis, Gajwani, Gross, Gumley, Lawrie, Schwannauer, Schultze-Lutter, Grent-‘t-Jong and Uhlhaas |
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Keywords | Schizophrenia heart-rate variability clinical high risk for psychosis (CHR-P) autonomic functioning resting heart rate |
Language | English |
License | Copyright © 2020 Kocsis, Gajwani, Gross, Gumley, Lawrie, Schwannauer, Schultze-Lutter, Grent-‘t-Jong and Uhlhaas. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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Notes | These authors share senior authorship Reviewed by: Cheryl Mary Corcoran, Mount Sinai Medical Center, United States; Xueling Zhu, Central South University, China Edited by: Maximus Berger, University of Melbourne, Australia This article was submitted to Psychopathology, a section of the journal Frontiers in Psychiatry |
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Snippet | Alterations in autonomic functioning in individuals diagnosed with schizophrenia are well-documented. Yet, it is currently unclear whether these dysfunctions... Introduction: Alterations in autonomic functioning in individuals diagnosed with schizophrenia are well-documented. Yet, it is currently unclear whether these... Introduction: Alterations in autonomic functioning in individuals diagnosed with schizophrenia are well-documented. Yet, it is currently unclear whether these... |
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SubjectTerms | autonomic functioning clinical high risk for psychosis (CHR-P) heart-rate variability Psychiatry resting heart rate Schizophrenia |
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Title | Altered Autonomic Function in Individuals at Clinical High Risk for Psychosis |
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