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Patient–clinician brain concordance underlies causal dynamics in nonverbal communication and negative affective expressivity
Patient–clinician concordance in behavior and brain activity has been proposed as a potential key mediator of mutual empathy and clinical rapport in the therapeutic encounter. However, the specific elements of patient–clinician communication that may support brain-to-brain concordance and therapeuti...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799700/ https://www.ncbi.nlm.nih.gov/pubmed/35091536 http://dx.doi.org/10.1038/s41398-022-01810-7 |
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author | Ellingsen, Dan-Mikael Duggento, Andrea Isenburg, Kylie Jung, Changjin Lee, Jeungchan Gerber, Jessica Mawla, Ishtiaq Sclocco, Roberta Edwards, Robert R. Kelley, John M. Kirsch, Irving Kaptchuk, Ted J. Toschi, Nicola Napadow, Vitaly |
author_facet | Ellingsen, Dan-Mikael Duggento, Andrea Isenburg, Kylie Jung, Changjin Lee, Jeungchan Gerber, Jessica Mawla, Ishtiaq Sclocco, Roberta Edwards, Robert R. Kelley, John M. Kirsch, Irving Kaptchuk, Ted J. Toschi, Nicola Napadow, Vitaly |
author_sort | Ellingsen, Dan-Mikael |
collection | PubMed |
description | Patient–clinician concordance in behavior and brain activity has been proposed as a potential key mediator of mutual empathy and clinical rapport in the therapeutic encounter. However, the specific elements of patient–clinician communication that may support brain-to-brain concordance and therapeutic alliance are unknown. Here, we investigated how pain-related, directional facial communication between patients and clinicians is associated with brain-to-brain concordance. Patient–clinician dyads interacted in a pain-treatment context, during synchronous assessment of brain activity (fMRI hyperscanning) and online video transfer, enabling face-to-face social interaction. In-scanner videos were used for automated individual facial action unit (AU) time-series extraction. First, an interpretable machine-learning classifier of patients’ facial expressions, from an independent fMRI experiment, significantly distinguished moderately painful leg pressure from innocuous pressure stimuli. Next, we estimated neural-network causality of patient-to-clinician directional information flow of facial expressions during clinician-initiated treatment of patients’ evoked pain. We identified a leader–follower relationship in which patients predominantly led the facial communication while clinicians responded to patients’ expressions. Finally, analyses of dynamic brain-to-brain concordance showed that patients’ mid/posterior insular concordance with the clinicians’ anterior insula cortex, a region identified in previously published data from this study(1), was associated with therapeutic alliance, and self-reported and objective (patient-to-clinician-directed causal influence) markers of negative-affect expressivity. These results suggest a role of patient-clinician concordance of the insula, a social-mirroring and salience-processing brain node, in mediating directional dynamics of pain-directed facial communication during therapeutic encounters. |
format | Online Article Text |
id | pubmed-8799700 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87997002022-02-07 Patient–clinician brain concordance underlies causal dynamics in nonverbal communication and negative affective expressivity Ellingsen, Dan-Mikael Duggento, Andrea Isenburg, Kylie Jung, Changjin Lee, Jeungchan Gerber, Jessica Mawla, Ishtiaq Sclocco, Roberta Edwards, Robert R. Kelley, John M. Kirsch, Irving Kaptchuk, Ted J. Toschi, Nicola Napadow, Vitaly Transl Psychiatry Article Patient–clinician concordance in behavior and brain activity has been proposed as a potential key mediator of mutual empathy and clinical rapport in the therapeutic encounter. However, the specific elements of patient–clinician communication that may support brain-to-brain concordance and therapeutic alliance are unknown. Here, we investigated how pain-related, directional facial communication between patients and clinicians is associated with brain-to-brain concordance. Patient–clinician dyads interacted in a pain-treatment context, during synchronous assessment of brain activity (fMRI hyperscanning) and online video transfer, enabling face-to-face social interaction. In-scanner videos were used for automated individual facial action unit (AU) time-series extraction. First, an interpretable machine-learning classifier of patients’ facial expressions, from an independent fMRI experiment, significantly distinguished moderately painful leg pressure from innocuous pressure stimuli. Next, we estimated neural-network causality of patient-to-clinician directional information flow of facial expressions during clinician-initiated treatment of patients’ evoked pain. We identified a leader–follower relationship in which patients predominantly led the facial communication while clinicians responded to patients’ expressions. Finally, analyses of dynamic brain-to-brain concordance showed that patients’ mid/posterior insular concordance with the clinicians’ anterior insula cortex, a region identified in previously published data from this study(1), was associated with therapeutic alliance, and self-reported and objective (patient-to-clinician-directed causal influence) markers of negative-affect expressivity. These results suggest a role of patient-clinician concordance of the insula, a social-mirroring and salience-processing brain node, in mediating directional dynamics of pain-directed facial communication during therapeutic encounters. Nature Publishing Group UK 2022-01-28 /pmc/articles/PMC8799700/ /pubmed/35091536 http://dx.doi.org/10.1038/s41398-022-01810-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ellingsen, Dan-Mikael Duggento, Andrea Isenburg, Kylie Jung, Changjin Lee, Jeungchan Gerber, Jessica Mawla, Ishtiaq Sclocco, Roberta Edwards, Robert R. Kelley, John M. Kirsch, Irving Kaptchuk, Ted J. Toschi, Nicola Napadow, Vitaly Patient–clinician brain concordance underlies causal dynamics in nonverbal communication and negative affective expressivity |
title | Patient–clinician brain concordance underlies causal dynamics in nonverbal communication and negative affective expressivity |
title_full | Patient–clinician brain concordance underlies causal dynamics in nonverbal communication and negative affective expressivity |
title_fullStr | Patient–clinician brain concordance underlies causal dynamics in nonverbal communication and negative affective expressivity |
title_full_unstemmed | Patient–clinician brain concordance underlies causal dynamics in nonverbal communication and negative affective expressivity |
title_short | Patient–clinician brain concordance underlies causal dynamics in nonverbal communication and negative affective expressivity |
title_sort | patient–clinician brain concordance underlies causal dynamics in nonverbal communication and negative affective expressivity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799700/ https://www.ncbi.nlm.nih.gov/pubmed/35091536 http://dx.doi.org/10.1038/s41398-022-01810-7 |
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