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Multiscale entropy and small-world network analysis in rs-fMRI — new tools to evaluate early basal ganglia dysfunction in diabetic peripheral neuropathy

OBJECTIVE: The risk of falling increases in diabetic peripheral neuropathy (DPN) patients. As a central part, Basal ganglia play an important role in motor and balance control, but whether its involvement in DPN is unclear. METHODS: Ten patients with confirmed DPN, ten diabetes patients without DPN,...

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Autores principales: Yuan, Geheng, Zheng, Yijia, Wang, Ye, Qi, Xin, Wang, Rui, Ma, Zhanyang, Guo, Xiaohui, Wang, Xiaoying, Zhang, Jue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672501/
https://www.ncbi.nlm.nih.gov/pubmed/36407323
http://dx.doi.org/10.3389/fendo.2022.974254
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author Yuan, Geheng
Zheng, Yijia
Wang, Ye
Qi, Xin
Wang, Rui
Ma, Zhanyang
Guo, Xiaohui
Wang, Xiaoying
Zhang, Jue
author_facet Yuan, Geheng
Zheng, Yijia
Wang, Ye
Qi, Xin
Wang, Rui
Ma, Zhanyang
Guo, Xiaohui
Wang, Xiaoying
Zhang, Jue
author_sort Yuan, Geheng
collection PubMed
description OBJECTIVE: The risk of falling increases in diabetic peripheral neuropathy (DPN) patients. As a central part, Basal ganglia play an important role in motor and balance control, but whether its involvement in DPN is unclear. METHODS: Ten patients with confirmed DPN, ten diabetes patients without DPN, and ten healthy age-matched controls(HC) were recruited to undergo magnetic resonance imaging(MRI) to assess brain structure and zone adaptability. Multiscale entropy and small-world network analysis were then used to assess the complexity of the hemodynamic response signal, reflecting the adaptability of the basal ganglia. RESULTS: There was no significant difference in brain structure among the three groups, except the duration of diabetes in DPN patients was longer (p < 0.05). The complexity of basal ganglia was significantly decreased in the DPN group compared with the non-DPN and HC group (p < 0.05), which suggested their poor adaptability. CONCLUSION: In the sensorimotor loop, peripheral and early central nervous lesions exist simultaneously in DPN patients. Multiscale Entropy and Small-world Network Analysis could detect basal ganglia dysfunction prior to structural changes in MRI, potentially valuable tools for early non-invasive screening and follow-up.
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spelling pubmed-96725012022-11-19 Multiscale entropy and small-world network analysis in rs-fMRI — new tools to evaluate early basal ganglia dysfunction in diabetic peripheral neuropathy Yuan, Geheng Zheng, Yijia Wang, Ye Qi, Xin Wang, Rui Ma, Zhanyang Guo, Xiaohui Wang, Xiaoying Zhang, Jue Front Endocrinol (Lausanne) Endocrinology OBJECTIVE: The risk of falling increases in diabetic peripheral neuropathy (DPN) patients. As a central part, Basal ganglia play an important role in motor and balance control, but whether its involvement in DPN is unclear. METHODS: Ten patients with confirmed DPN, ten diabetes patients without DPN, and ten healthy age-matched controls(HC) were recruited to undergo magnetic resonance imaging(MRI) to assess brain structure and zone adaptability. Multiscale entropy and small-world network analysis were then used to assess the complexity of the hemodynamic response signal, reflecting the adaptability of the basal ganglia. RESULTS: There was no significant difference in brain structure among the three groups, except the duration of diabetes in DPN patients was longer (p < 0.05). The complexity of basal ganglia was significantly decreased in the DPN group compared with the non-DPN and HC group (p < 0.05), which suggested their poor adaptability. CONCLUSION: In the sensorimotor loop, peripheral and early central nervous lesions exist simultaneously in DPN patients. Multiscale Entropy and Small-world Network Analysis could detect basal ganglia dysfunction prior to structural changes in MRI, potentially valuable tools for early non-invasive screening and follow-up. Frontiers Media S.A. 2022-11-04 /pmc/articles/PMC9672501/ /pubmed/36407323 http://dx.doi.org/10.3389/fendo.2022.974254 Text en Copyright © 2022 Yuan, Zheng, Wang, Qi, Wang, Ma, Guo, Wang and Zhang https://creativecommons.org/licenses/by/4.0/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.
spellingShingle Endocrinology
Yuan, Geheng
Zheng, Yijia
Wang, Ye
Qi, Xin
Wang, Rui
Ma, Zhanyang
Guo, Xiaohui
Wang, Xiaoying
Zhang, Jue
Multiscale entropy and small-world network analysis in rs-fMRI — new tools to evaluate early basal ganglia dysfunction in diabetic peripheral neuropathy
title Multiscale entropy and small-world network analysis in rs-fMRI — new tools to evaluate early basal ganglia dysfunction in diabetic peripheral neuropathy
title_full Multiscale entropy and small-world network analysis in rs-fMRI — new tools to evaluate early basal ganglia dysfunction in diabetic peripheral neuropathy
title_fullStr Multiscale entropy and small-world network analysis in rs-fMRI — new tools to evaluate early basal ganglia dysfunction in diabetic peripheral neuropathy
title_full_unstemmed Multiscale entropy and small-world network analysis in rs-fMRI — new tools to evaluate early basal ganglia dysfunction in diabetic peripheral neuropathy
title_short Multiscale entropy and small-world network analysis in rs-fMRI — new tools to evaluate early basal ganglia dysfunction in diabetic peripheral neuropathy
title_sort multiscale entropy and small-world network analysis in rs-fmri — new tools to evaluate early basal ganglia dysfunction in diabetic peripheral neuropathy
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672501/
https://www.ncbi.nlm.nih.gov/pubmed/36407323
http://dx.doi.org/10.3389/fendo.2022.974254
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