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Altered insula–default mode network connectivity in fibromyalgia: a resting-state magnetoencephalographic study

BACKGROUND: Fibromyalgia (FM) is a disabling chronic pain syndrome with unknown pathophysiology. Functional magnetic resonance imaging studies on FM have suggested altered brain connectivity between the insula and the default mode network (DMN). However, this connectivity change has not been charact...

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Autores principales: Hsiao, Fu-Jung, Wang, Shuu-Jiun, Lin, Yung-Yang, Fuh, Jong-Ling, Ko, Yu-Chieh, Wang, Pei-Ning, Chen, Wei-Ta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567574/
https://www.ncbi.nlm.nih.gov/pubmed/28831711
http://dx.doi.org/10.1186/s10194-017-0799-x
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author Hsiao, Fu-Jung
Wang, Shuu-Jiun
Lin, Yung-Yang
Fuh, Jong-Ling
Ko, Yu-Chieh
Wang, Pei-Ning
Chen, Wei-Ta
author_facet Hsiao, Fu-Jung
Wang, Shuu-Jiun
Lin, Yung-Yang
Fuh, Jong-Ling
Ko, Yu-Chieh
Wang, Pei-Ning
Chen, Wei-Ta
author_sort Hsiao, Fu-Jung
collection PubMed
description BACKGROUND: Fibromyalgia (FM) is a disabling chronic pain syndrome with unknown pathophysiology. Functional magnetic resonance imaging studies on FM have suggested altered brain connectivity between the insula and the default mode network (DMN). However, this connectivity change has not been characterized through direct neural signals for exploring the embedded spectrotemporal features and the pertinent clinical relevance. METHODS: We recorded the resting-state magnetoencephalographic activities of 28 patients with FM and 28 age- and sex-matched controls, and analyzed the source-based functional connectivity between the insula and the DMN at 1–40 Hz by using the minimum norm estimates and imaginary coherence methods. We also measured the connectivity between the DMN and the primary visual (V1) and somatosensory (S1) cortices as intrapatient negative controls. Connectivity measurement was further correlated with the clinical parameters of FM. RESULTS: Compared with the controls, patients with FM reported more tender points (15.2±2.0 vs. 5.9±3.7) and higher total tenderness score (TTS; 29.1±7.0 vs. 7.7±5.5; both p < 0.001); they also had decreased insula–DMN connectivity at the theta band (4–8 Hz; left, p = 0.007; right, p = 0.035), but displayed unchanged V1–DMN and S1–DMN connectivity (p > 0.05). When patients with FM and the controls were combined together, the insula-DMN theta connectivity was negatively correlated with the number of tender points (left insula, r = −0.428, p = 0.001; right insula, r = −0.4, p = 0.002) and TTS score (left insula, r = −0.429, p = 0.001; right insula, r = −0.389, p = 0.003). Furthermore, in patients with FM, the right insula–DMN connectivity at the beta band (13–25 Hz) was negatively correlated with the number of tender points (r = −0.532, p = 0.004) and TTS (r = −0.428, p = 0.023), and the bilateral insula–DMN connectivity at the delta band (1–4 Hz) was negatively correlated with FM Symptom Severity (left: r = −0.423, p = 0.025; right: r = −0.437, p = 0.020) and functional disability (Fibromyalgia Impact Questionnaire; left: r = −0.415, p = 0.028; right: r = −0.374, p = 0.050). CONCLUSIONS: We confirmed the frequency-specific reorganization of the insula–DMN connectivity in FM. The clinical relevance of this connectivity change may warrant future studies to elucidate its causal relationship and potential as a neurological signature for FM. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s10194-017-0799-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-55675742017-09-11 Altered insula–default mode network connectivity in fibromyalgia: a resting-state magnetoencephalographic study Hsiao, Fu-Jung Wang, Shuu-Jiun Lin, Yung-Yang Fuh, Jong-Ling Ko, Yu-Chieh Wang, Pei-Ning Chen, Wei-Ta J Headache Pain Research Article BACKGROUND: Fibromyalgia (FM) is a disabling chronic pain syndrome with unknown pathophysiology. Functional magnetic resonance imaging studies on FM have suggested altered brain connectivity between the insula and the default mode network (DMN). However, this connectivity change has not been characterized through direct neural signals for exploring the embedded spectrotemporal features and the pertinent clinical relevance. METHODS: We recorded the resting-state magnetoencephalographic activities of 28 patients with FM and 28 age- and sex-matched controls, and analyzed the source-based functional connectivity between the insula and the DMN at 1–40 Hz by using the minimum norm estimates and imaginary coherence methods. We also measured the connectivity between the DMN and the primary visual (V1) and somatosensory (S1) cortices as intrapatient negative controls. Connectivity measurement was further correlated with the clinical parameters of FM. RESULTS: Compared with the controls, patients with FM reported more tender points (15.2±2.0 vs. 5.9±3.7) and higher total tenderness score (TTS; 29.1±7.0 vs. 7.7±5.5; both p < 0.001); they also had decreased insula–DMN connectivity at the theta band (4–8 Hz; left, p = 0.007; right, p = 0.035), but displayed unchanged V1–DMN and S1–DMN connectivity (p > 0.05). When patients with FM and the controls were combined together, the insula-DMN theta connectivity was negatively correlated with the number of tender points (left insula, r = −0.428, p = 0.001; right insula, r = −0.4, p = 0.002) and TTS score (left insula, r = −0.429, p = 0.001; right insula, r = −0.389, p = 0.003). Furthermore, in patients with FM, the right insula–DMN connectivity at the beta band (13–25 Hz) was negatively correlated with the number of tender points (r = −0.532, p = 0.004) and TTS (r = −0.428, p = 0.023), and the bilateral insula–DMN connectivity at the delta band (1–4 Hz) was negatively correlated with FM Symptom Severity (left: r = −0.423, p = 0.025; right: r = −0.437, p = 0.020) and functional disability (Fibromyalgia Impact Questionnaire; left: r = −0.415, p = 0.028; right: r = −0.374, p = 0.050). CONCLUSIONS: We confirmed the frequency-specific reorganization of the insula–DMN connectivity in FM. The clinical relevance of this connectivity change may warrant future studies to elucidate its causal relationship and potential as a neurological signature for FM. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s10194-017-0799-x) contains supplementary material, which is available to authorized users. Springer Milan 2017-08-23 /pmc/articles/PMC5567574/ /pubmed/28831711 http://dx.doi.org/10.1186/s10194-017-0799-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Research Article
Hsiao, Fu-Jung
Wang, Shuu-Jiun
Lin, Yung-Yang
Fuh, Jong-Ling
Ko, Yu-Chieh
Wang, Pei-Ning
Chen, Wei-Ta
Altered insula–default mode network connectivity in fibromyalgia: a resting-state magnetoencephalographic study
title Altered insula–default mode network connectivity in fibromyalgia: a resting-state magnetoencephalographic study
title_full Altered insula–default mode network connectivity in fibromyalgia: a resting-state magnetoencephalographic study
title_fullStr Altered insula–default mode network connectivity in fibromyalgia: a resting-state magnetoencephalographic study
title_full_unstemmed Altered insula–default mode network connectivity in fibromyalgia: a resting-state magnetoencephalographic study
title_short Altered insula–default mode network connectivity in fibromyalgia: a resting-state magnetoencephalographic study
title_sort altered insula–default mode network connectivity in fibromyalgia: a resting-state magnetoencephalographic study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567574/
https://www.ncbi.nlm.nih.gov/pubmed/28831711
http://dx.doi.org/10.1186/s10194-017-0799-x
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