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Osteopathy modulates brain–heart interaction in chronic pain patients: an ASL study

In this study we used a combination of measures including regional cerebral blood flow (rCBF) and heart rate variability (HRV) to investigate brain–heart correlates of longitudinal baseline changes of chronic low back pain (cLBP) after osteopathic manipulative treatment (OMT). Thirty-two right-hande...

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Autores principales: Cerritelli, Francesco, Chiacchiaretta, Piero, Gambi, Francesco, Saggini, Raoul, Perrucci, Mauro Gianni, Ferretti, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907192/
https://www.ncbi.nlm.nih.gov/pubmed/33633195
http://dx.doi.org/10.1038/s41598-021-83893-8
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author Cerritelli, Francesco
Chiacchiaretta, Piero
Gambi, Francesco
Saggini, Raoul
Perrucci, Mauro Gianni
Ferretti, Antonio
author_facet Cerritelli, Francesco
Chiacchiaretta, Piero
Gambi, Francesco
Saggini, Raoul
Perrucci, Mauro Gianni
Ferretti, Antonio
author_sort Cerritelli, Francesco
collection PubMed
description In this study we used a combination of measures including regional cerebral blood flow (rCBF) and heart rate variability (HRV) to investigate brain–heart correlates of longitudinal baseline changes of chronic low back pain (cLBP) after osteopathic manipulative treatment (OMT). Thirty-two right-handed patients were randomised and divided into 4 weekly session of OMT (N = 16) or Sham (N = 16). Participants aged 42.3 ± 7.3 (M/F: 20/12) with cLBP (duration: 14.6 ± 8.0 m). At the end of the study, patients receiving OMT showed decreased baseline rCBF within several regions belonging to the pain matrix (left posterior insula, left anterior cingulate cortex, left thalamus), sensory regions (left superior parietal lobe), middle frontal lobe and left cuneus. Conversely, rCBF was increased in right anterior insula, bilateral striatum, left posterior cingulate cortex, right prefrontal cortex, left cerebellum and right ventroposterior lateral thalamus in the OMT group as compared with Sham. OMT showed a statistically significant negative correlation between baseline High Frequency HRV changes and rCBF changes at T2 in the left posterior insula and bilateral lentiform nucleus. The same brain regions showed a positive correlation between rCBF changes and Low Frequency HRV baseline changes at T2. These findings suggest that OMT can play a significant role in regulating brain–heart interaction mechanisms.
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spelling pubmed-79071922021-02-26 Osteopathy modulates brain–heart interaction in chronic pain patients: an ASL study Cerritelli, Francesco Chiacchiaretta, Piero Gambi, Francesco Saggini, Raoul Perrucci, Mauro Gianni Ferretti, Antonio Sci Rep Article In this study we used a combination of measures including regional cerebral blood flow (rCBF) and heart rate variability (HRV) to investigate brain–heart correlates of longitudinal baseline changes of chronic low back pain (cLBP) after osteopathic manipulative treatment (OMT). Thirty-two right-handed patients were randomised and divided into 4 weekly session of OMT (N = 16) or Sham (N = 16). Participants aged 42.3 ± 7.3 (M/F: 20/12) with cLBP (duration: 14.6 ± 8.0 m). At the end of the study, patients receiving OMT showed decreased baseline rCBF within several regions belonging to the pain matrix (left posterior insula, left anterior cingulate cortex, left thalamus), sensory regions (left superior parietal lobe), middle frontal lobe and left cuneus. Conversely, rCBF was increased in right anterior insula, bilateral striatum, left posterior cingulate cortex, right prefrontal cortex, left cerebellum and right ventroposterior lateral thalamus in the OMT group as compared with Sham. OMT showed a statistically significant negative correlation between baseline High Frequency HRV changes and rCBF changes at T2 in the left posterior insula and bilateral lentiform nucleus. The same brain regions showed a positive correlation between rCBF changes and Low Frequency HRV baseline changes at T2. These findings suggest that OMT can play a significant role in regulating brain–heart interaction mechanisms. Nature Publishing Group UK 2021-02-25 /pmc/articles/PMC7907192/ /pubmed/33633195 http://dx.doi.org/10.1038/s41598-021-83893-8 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Cerritelli, Francesco
Chiacchiaretta, Piero
Gambi, Francesco
Saggini, Raoul
Perrucci, Mauro Gianni
Ferretti, Antonio
Osteopathy modulates brain–heart interaction in chronic pain patients: an ASL study
title Osteopathy modulates brain–heart interaction in chronic pain patients: an ASL study
title_full Osteopathy modulates brain–heart interaction in chronic pain patients: an ASL study
title_fullStr Osteopathy modulates brain–heart interaction in chronic pain patients: an ASL study
title_full_unstemmed Osteopathy modulates brain–heart interaction in chronic pain patients: an ASL study
title_short Osteopathy modulates brain–heart interaction in chronic pain patients: an ASL study
title_sort osteopathy modulates brain–heart interaction in chronic pain patients: an asl study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907192/
https://www.ncbi.nlm.nih.gov/pubmed/33633195
http://dx.doi.org/10.1038/s41598-021-83893-8
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