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Phase angle in localized bioimpedance measurements to assess and monitor muscle injury

Localized bioimpedance (L-BIA) measurements are an innovative method to non-invasively identify structural derangement of soft tissues, principally muscles, and fluid accumulation in response to traumatic injury. This review provides unique L-BIA data demonstrating significant relative differences b...

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Autores principales: Nescolarde, Lexa, Talluri, Antonio, Yanguas, Javier, Lukaski, Henry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10140135/
https://www.ncbi.nlm.nih.gov/pubmed/36847994
http://dx.doi.org/10.1007/s11154-023-09790-9
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author Nescolarde, Lexa
Talluri, Antonio
Yanguas, Javier
Lukaski, Henry
author_facet Nescolarde, Lexa
Talluri, Antonio
Yanguas, Javier
Lukaski, Henry
author_sort Nescolarde, Lexa
collection PubMed
description Localized bioimpedance (L-BIA) measurements are an innovative method to non-invasively identify structural derangement of soft tissues, principally muscles, and fluid accumulation in response to traumatic injury. This review provides unique L-BIA data demonstrating significant relative differences between injured and contralateral non-injured regions of interest (ROI) associated with soft tissue injury. One key finding is the specific and sensitive role of reactance (Xc), measured at 50 kHz with a phase-sensitive BI instrument, to identify objective degrees of muscle injury, localized structural damage and fluid accretion, determined using magnetic resonance imaging. The predominant effect of Xc as an indicator of severity of muscle injury is highlighted in phase angle (PhA) measurements. Novel experimental models utilizing cooking-induced cell disruption, saline injection into meat specimens, and measurements of changing amounts of cells in a constant volume provide empirical evidence of the physiological correlates of series Xc as cells in water. Findings of strong associations of capacitance, computed from parallel Xc (X(CP)), with whole body counting of 40-potassium and resting metabolic rate support the hypothesis that parallel Xc is a biomarker of body cell mass. These observations provide a theoretical and practical basis for a significant role of Xc, and hence PhA, to identify objectively graded muscle injury and to reliably monitor progress of treatment and return of muscle function.
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spelling pubmed-101401352023-04-29 Phase angle in localized bioimpedance measurements to assess and monitor muscle injury Nescolarde, Lexa Talluri, Antonio Yanguas, Javier Lukaski, Henry Rev Endocr Metab Disord Article Localized bioimpedance (L-BIA) measurements are an innovative method to non-invasively identify structural derangement of soft tissues, principally muscles, and fluid accumulation in response to traumatic injury. This review provides unique L-BIA data demonstrating significant relative differences between injured and contralateral non-injured regions of interest (ROI) associated with soft tissue injury. One key finding is the specific and sensitive role of reactance (Xc), measured at 50 kHz with a phase-sensitive BI instrument, to identify objective degrees of muscle injury, localized structural damage and fluid accretion, determined using magnetic resonance imaging. The predominant effect of Xc as an indicator of severity of muscle injury is highlighted in phase angle (PhA) measurements. Novel experimental models utilizing cooking-induced cell disruption, saline injection into meat specimens, and measurements of changing amounts of cells in a constant volume provide empirical evidence of the physiological correlates of series Xc as cells in water. Findings of strong associations of capacitance, computed from parallel Xc (X(CP)), with whole body counting of 40-potassium and resting metabolic rate support the hypothesis that parallel Xc is a biomarker of body cell mass. These observations provide a theoretical and practical basis for a significant role of Xc, and hence PhA, to identify objectively graded muscle injury and to reliably monitor progress of treatment and return of muscle function. Springer US 2023-02-27 2023 /pmc/articles/PMC10140135/ /pubmed/36847994 http://dx.doi.org/10.1007/s11154-023-09790-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Nescolarde, Lexa
Talluri, Antonio
Yanguas, Javier
Lukaski, Henry
Phase angle in localized bioimpedance measurements to assess and monitor muscle injury
title Phase angle in localized bioimpedance measurements to assess and monitor muscle injury
title_full Phase angle in localized bioimpedance measurements to assess and monitor muscle injury
title_fullStr Phase angle in localized bioimpedance measurements to assess and monitor muscle injury
title_full_unstemmed Phase angle in localized bioimpedance measurements to assess and monitor muscle injury
title_short Phase angle in localized bioimpedance measurements to assess and monitor muscle injury
title_sort phase angle in localized bioimpedance measurements to assess and monitor muscle injury
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10140135/
https://www.ncbi.nlm.nih.gov/pubmed/36847994
http://dx.doi.org/10.1007/s11154-023-09790-9
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