Aberrant functional connectivity and temporal variability of the dynamic pain connectome in patients with low back related leg pain

Abstract Neuroimaging studies have suggested a link between the intensity of chronic low back pain intensity and structural and functional brain alterations. However, chronic pain results from the coordination and dynamics among several brain networks that comprise the dynamic pain connectome. Here,...

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Main Authors: Yixiu Pei, Jidong Peng, Yong Zhang, Muhua Huang, Fuqing Zhou
Format: Article
Language:English
Published: Nature Portfolio 2022-04-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-022-10238-4
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author Yixiu Pei
Jidong Peng
Yong Zhang
Muhua Huang
Fuqing Zhou
author_facet Yixiu Pei
Jidong Peng
Yong Zhang
Muhua Huang
Fuqing Zhou
author_sort Yixiu Pei
collection DOAJ
description Abstract Neuroimaging studies have suggested a link between the intensity of chronic low back pain intensity and structural and functional brain alterations. However, chronic pain results from the coordination and dynamics among several brain networks that comprise the dynamic pain connectome. Here, we use resting-state functional magnetic resonance imaging and measures of static (sFC) and dynamic functional connectivity (dFC) variability in the typical (0.01–0.1 Hz) and five specific (slow-6 to slow-2) frequency bands to test hypotheses regarding disruption in this variability in low back-related leg pain (LBLP) patients who experience chronic pain and numbness. Twenty-four LBLP patients and 23 healthy controls completed clinical assessments, and partial correlational analyses between altered sFC and dFC variability and clinical measures were conducted. We found a lower within-network sFC in the ascending nociceptive pathway (Asc) and a lower cross-network sFC between nodes of the salience network and the Asc in the typical frequency band. In the slow-5 frequency band, a lower within-network sFC was found in the Asc. Abnormal cross-network sFC was found between nodes of the salience network-Asc (slow-5 and slow-6) and the default mode network-Asc (slow-4 and slow-6). Furthermore, cross-network abnormalities in the typical and certain specific frequency bands were linked to clinical assessments. These findings indicate that frequency-related within- and cross-network communication among the nodes in the dynamic pain connectome is dysfunctional in LBLP patients and that selecting specific frequencies may be potentially useful for detecting LBLP-related brain activity.
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spelling doaj.art-1429e7089a8848b3b0331e4a4f9feed52022-12-22T01:51:28ZengNature PortfolioScientific Reports2045-23222022-04-0112111210.1038/s41598-022-10238-4Aberrant functional connectivity and temporal variability of the dynamic pain connectome in patients with low back related leg painYixiu Pei0Jidong Peng1Yong Zhang2Muhua Huang3Fuqing Zhou4Department of Radiology, The First Affiliated Hospital, Nanchang UniversityDepartment of Medical Imaging, The Affiliated Ganzhou Hospital of Nanchang UniversityDepartment of Pain Clinic, The First Affiliated Hospital, Nanchang UniversityDepartment of Radiology, The First Affiliated Hospital, Nanchang UniversityDepartment of Radiology, The First Affiliated Hospital, Nanchang UniversityAbstract Neuroimaging studies have suggested a link between the intensity of chronic low back pain intensity and structural and functional brain alterations. However, chronic pain results from the coordination and dynamics among several brain networks that comprise the dynamic pain connectome. Here, we use resting-state functional magnetic resonance imaging and measures of static (sFC) and dynamic functional connectivity (dFC) variability in the typical (0.01–0.1 Hz) and five specific (slow-6 to slow-2) frequency bands to test hypotheses regarding disruption in this variability in low back-related leg pain (LBLP) patients who experience chronic pain and numbness. Twenty-four LBLP patients and 23 healthy controls completed clinical assessments, and partial correlational analyses between altered sFC and dFC variability and clinical measures were conducted. We found a lower within-network sFC in the ascending nociceptive pathway (Asc) and a lower cross-network sFC between nodes of the salience network and the Asc in the typical frequency band. In the slow-5 frequency band, a lower within-network sFC was found in the Asc. Abnormal cross-network sFC was found between nodes of the salience network-Asc (slow-5 and slow-6) and the default mode network-Asc (slow-4 and slow-6). Furthermore, cross-network abnormalities in the typical and certain specific frequency bands were linked to clinical assessments. These findings indicate that frequency-related within- and cross-network communication among the nodes in the dynamic pain connectome is dysfunctional in LBLP patients and that selecting specific frequencies may be potentially useful for detecting LBLP-related brain activity.https://doi.org/10.1038/s41598-022-10238-4
spellingShingle Yixiu Pei
Jidong Peng
Yong Zhang
Muhua Huang
Fuqing Zhou
Aberrant functional connectivity and temporal variability of the dynamic pain connectome in patients with low back related leg pain
Scientific Reports
title Aberrant functional connectivity and temporal variability of the dynamic pain connectome in patients with low back related leg pain
title_full Aberrant functional connectivity and temporal variability of the dynamic pain connectome in patients with low back related leg pain
title_fullStr Aberrant functional connectivity and temporal variability of the dynamic pain connectome in patients with low back related leg pain
title_full_unstemmed Aberrant functional connectivity and temporal variability of the dynamic pain connectome in patients with low back related leg pain
title_short Aberrant functional connectivity and temporal variability of the dynamic pain connectome in patients with low back related leg pain
title_sort aberrant functional connectivity and temporal variability of the dynamic pain connectome in patients with low back related leg pain
url https://doi.org/10.1038/s41598-022-10238-4
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