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Neural Signatures of Handgrip Fatigue in Type 1 Diabetic Men and Women

Type 1 diabetes (T1D) is associated with reduced muscular strength and greater muscle fatigability. Along with changes in muscular mechanisms, T1D is also linked to structural changes in the brain. How the neurophysiological mechanisms underlying muscle fatigue is altered with T1D and sex related di...

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Autores principales: Tyagi, Oshin, Zhu, Yibo, Johnson, Connor, Mehta, Ranjana K., Sasangohar, Farzan, Erraguntla, Madhav, Qaraqe, Khalid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7680760/
https://www.ncbi.nlm.nih.gov/pubmed/33240061
http://dx.doi.org/10.3389/fnhum.2020.564969
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author Tyagi, Oshin
Zhu, Yibo
Johnson, Connor
Mehta, Ranjana K.
Sasangohar, Farzan
Erraguntla, Madhav
Qaraqe, Khalid
author_facet Tyagi, Oshin
Zhu, Yibo
Johnson, Connor
Mehta, Ranjana K.
Sasangohar, Farzan
Erraguntla, Madhav
Qaraqe, Khalid
author_sort Tyagi, Oshin
collection PubMed
description Type 1 diabetes (T1D) is associated with reduced muscular strength and greater muscle fatigability. Along with changes in muscular mechanisms, T1D is also linked to structural changes in the brain. How the neurophysiological mechanisms underlying muscle fatigue is altered with T1D and sex related differences of these mechanisms are still not well investigated. The aim of this study was to determine the impact of T1D on the neural correlates of handgrip fatigue and examine sex and T1D related differences in neuromuscular performance parameters, neural activation and functional connectivity patterns between the motor regions of the brain. Forty-two adults, balanced by condition (healthy vs T1D) and sex (male vs female), and performed submaximal isometric handgrip contractions until voluntary exhaustion. Initial strength, endurance time, strength loss, force variability, and complexity measures were collected. Additionally, hemodynamic responses from motor-function related cortical regions, using functional near-infrared spectroscopy (fNIRS), were obtained. Overall, females exhibited lower initial strength (p < 0.0001), and greater strength loss (p = 0.023) than males. While initial strength was significantly lower in the T1D group (p = 0.012) compared to the healthy group, endurance times and strength loss were comparable between the two groups. Force complexity, measured as approximate entropy, was found to be lower throughout the experiment for the T1D group (p = 0.0378), indicating lower online motor adaptability. Although, T1D and healthy groups fatigued similarly, only the T1D group exhibited increased neural activation in the left (p = 0.095) and right (p = 0.072) supplementary motor areas (SMA) over time. A sex × condition × fatigue interaction effect (p = 0.044) showed that while increased activation was observed in both T1D females and healthy males from the Early to Middle phase, this was not observed in healthy females or T1D males. These findings demonstrate that T1D adults had lower adaptability to fatigue which they compensated for by increasing neural effort. This study highlights the importance of examining both neural and motor performance signatures when investigating the impact of chronic conditions on neuromuscular fatigue. Additionally, the findings have implications for developing intervention strategies for training, rehabilitation, and ergonomics considerations for individuals with chronic conditions.
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spelling pubmed-76807602020-11-24 Neural Signatures of Handgrip Fatigue in Type 1 Diabetic Men and Women Tyagi, Oshin Zhu, Yibo Johnson, Connor Mehta, Ranjana K. Sasangohar, Farzan Erraguntla, Madhav Qaraqe, Khalid Front Hum Neurosci Neuroscience Type 1 diabetes (T1D) is associated with reduced muscular strength and greater muscle fatigability. Along with changes in muscular mechanisms, T1D is also linked to structural changes in the brain. How the neurophysiological mechanisms underlying muscle fatigue is altered with T1D and sex related differences of these mechanisms are still not well investigated. The aim of this study was to determine the impact of T1D on the neural correlates of handgrip fatigue and examine sex and T1D related differences in neuromuscular performance parameters, neural activation and functional connectivity patterns between the motor regions of the brain. Forty-two adults, balanced by condition (healthy vs T1D) and sex (male vs female), and performed submaximal isometric handgrip contractions until voluntary exhaustion. Initial strength, endurance time, strength loss, force variability, and complexity measures were collected. Additionally, hemodynamic responses from motor-function related cortical regions, using functional near-infrared spectroscopy (fNIRS), were obtained. Overall, females exhibited lower initial strength (p < 0.0001), and greater strength loss (p = 0.023) than males. While initial strength was significantly lower in the T1D group (p = 0.012) compared to the healthy group, endurance times and strength loss were comparable between the two groups. Force complexity, measured as approximate entropy, was found to be lower throughout the experiment for the T1D group (p = 0.0378), indicating lower online motor adaptability. Although, T1D and healthy groups fatigued similarly, only the T1D group exhibited increased neural activation in the left (p = 0.095) and right (p = 0.072) supplementary motor areas (SMA) over time. A sex × condition × fatigue interaction effect (p = 0.044) showed that while increased activation was observed in both T1D females and healthy males from the Early to Middle phase, this was not observed in healthy females or T1D males. These findings demonstrate that T1D adults had lower adaptability to fatigue which they compensated for by increasing neural effort. This study highlights the importance of examining both neural and motor performance signatures when investigating the impact of chronic conditions on neuromuscular fatigue. Additionally, the findings have implications for developing intervention strategies for training, rehabilitation, and ergonomics considerations for individuals with chronic conditions. Frontiers Media S.A. 2020-11-09 /pmc/articles/PMC7680760/ /pubmed/33240061 http://dx.doi.org/10.3389/fnhum.2020.564969 Text en Copyright © 2020 Tyagi, Zhu, Johnson, Mehta, Sasangohar, Erraguntla and Qaraqe. http://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 Neuroscience
Tyagi, Oshin
Zhu, Yibo
Johnson, Connor
Mehta, Ranjana K.
Sasangohar, Farzan
Erraguntla, Madhav
Qaraqe, Khalid
Neural Signatures of Handgrip Fatigue in Type 1 Diabetic Men and Women
title Neural Signatures of Handgrip Fatigue in Type 1 Diabetic Men and Women
title_full Neural Signatures of Handgrip Fatigue in Type 1 Diabetic Men and Women
title_fullStr Neural Signatures of Handgrip Fatigue in Type 1 Diabetic Men and Women
title_full_unstemmed Neural Signatures of Handgrip Fatigue in Type 1 Diabetic Men and Women
title_short Neural Signatures of Handgrip Fatigue in Type 1 Diabetic Men and Women
title_sort neural signatures of handgrip fatigue in type 1 diabetic men and women
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7680760/
https://www.ncbi.nlm.nih.gov/pubmed/33240061
http://dx.doi.org/10.3389/fnhum.2020.564969
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