Cargando…
Elevated level of the soluble receptor for advanced glycation end-products involved in sarcopenia: an observational study
BACKGROUND: The soluble receptor for advanced glycation end products (sRAGE) has been proposed to serve as a marker for disease severity, but its role in sarcopenia, an age-related progressive loss of muscle mass and function, remains elusive. This study examines the association between sRAGE and sa...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495916/ https://www.ncbi.nlm.nih.gov/pubmed/34620111 http://dx.doi.org/10.1186/s12877-021-02487-1 |
_version_ | 1784579648526483456 |
---|---|
author | Wu, Shou-En Chiu, Yi-Lin Kao, Tung-Wei Chen, Wei-Liang |
author_facet | Wu, Shou-En Chiu, Yi-Lin Kao, Tung-Wei Chen, Wei-Liang |
author_sort | Wu, Shou-En |
collection | PubMed |
description | BACKGROUND: The soluble receptor for advanced glycation end products (sRAGE) has been proposed to serve as a marker for disease severity, but its role in sarcopenia, an age-related progressive loss of muscle mass and function, remains elusive. This study examines the association between sRAGE and sarcopenia. METHODS: A total of 314 community-dwelling elderly adults who had their health examination at Tri-Service General Hospital from 2017 to 2019 underwent protein analysis with enzyme-linked immunosorbent assay. The relationship with sarcopenia and its detailed information, including components and diagnosis status, were examined using linear and logistic regressions. RESULTS: As for sarcopenia components, low muscle mass (β = 162.8, p = 0.012) and strength (β = 181.31, p = 0.011) were significantly correlated with sRAGE, but not low gait speed (p = 0.066). With regard to disease status, confirmed sarcopenia (β = 436.93, p < 0.001), but not probable (p = 0.448) or severe sarcopenia (p = 0.488), was significantly correlated with sRAGE. In addition, females revealed a stronger association with sRAGE level by showing significant correlations with low muscle mass (β = 221.72, p = 0.014) and low muscle strength (β = 208.68, p = 0.043). CONCLUSIONS: sRAGE level showed a positive association with sarcopenia, illustrating its involvement in the evolution of sarcopenia. This association is more evident in female groups, which may be attributed to the loss of protection from estrogen in postmenopausal women. Utilizing sRAGE level as a prospective marker for sarcopenia deserves further investigation in future studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12877-021-02487-1. |
format | Online Article Text |
id | pubmed-8495916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84959162021-10-07 Elevated level of the soluble receptor for advanced glycation end-products involved in sarcopenia: an observational study Wu, Shou-En Chiu, Yi-Lin Kao, Tung-Wei Chen, Wei-Liang BMC Geriatr Research BACKGROUND: The soluble receptor for advanced glycation end products (sRAGE) has been proposed to serve as a marker for disease severity, but its role in sarcopenia, an age-related progressive loss of muscle mass and function, remains elusive. This study examines the association between sRAGE and sarcopenia. METHODS: A total of 314 community-dwelling elderly adults who had their health examination at Tri-Service General Hospital from 2017 to 2019 underwent protein analysis with enzyme-linked immunosorbent assay. The relationship with sarcopenia and its detailed information, including components and diagnosis status, were examined using linear and logistic regressions. RESULTS: As for sarcopenia components, low muscle mass (β = 162.8, p = 0.012) and strength (β = 181.31, p = 0.011) were significantly correlated with sRAGE, but not low gait speed (p = 0.066). With regard to disease status, confirmed sarcopenia (β = 436.93, p < 0.001), but not probable (p = 0.448) or severe sarcopenia (p = 0.488), was significantly correlated with sRAGE. In addition, females revealed a stronger association with sRAGE level by showing significant correlations with low muscle mass (β = 221.72, p = 0.014) and low muscle strength (β = 208.68, p = 0.043). CONCLUSIONS: sRAGE level showed a positive association with sarcopenia, illustrating its involvement in the evolution of sarcopenia. This association is more evident in female groups, which may be attributed to the loss of protection from estrogen in postmenopausal women. Utilizing sRAGE level as a prospective marker for sarcopenia deserves further investigation in future studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12877-021-02487-1. BioMed Central 2021-10-07 /pmc/articles/PMC8495916/ /pubmed/34620111 http://dx.doi.org/10.1186/s12877-021-02487-1 Text en © The Author(s) 2021 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Wu, Shou-En Chiu, Yi-Lin Kao, Tung-Wei Chen, Wei-Liang Elevated level of the soluble receptor for advanced glycation end-products involved in sarcopenia: an observational study |
title | Elevated level of the soluble receptor for advanced glycation end-products involved in sarcopenia: an observational study |
title_full | Elevated level of the soluble receptor for advanced glycation end-products involved in sarcopenia: an observational study |
title_fullStr | Elevated level of the soluble receptor for advanced glycation end-products involved in sarcopenia: an observational study |
title_full_unstemmed | Elevated level of the soluble receptor for advanced glycation end-products involved in sarcopenia: an observational study |
title_short | Elevated level of the soluble receptor for advanced glycation end-products involved in sarcopenia: an observational study |
title_sort | elevated level of the soluble receptor for advanced glycation end-products involved in sarcopenia: an observational study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495916/ https://www.ncbi.nlm.nih.gov/pubmed/34620111 http://dx.doi.org/10.1186/s12877-021-02487-1 |
work_keys_str_mv | AT wushouen elevatedlevelofthesolublereceptorforadvancedglycationendproductsinvolvedinsarcopeniaanobservationalstudy AT chiuyilin elevatedlevelofthesolublereceptorforadvancedglycationendproductsinvolvedinsarcopeniaanobservationalstudy AT kaotungwei elevatedlevelofthesolublereceptorforadvancedglycationendproductsinvolvedinsarcopeniaanobservationalstudy AT chenweiliang elevatedlevelofthesolublereceptorforadvancedglycationendproductsinvolvedinsarcopeniaanobservationalstudy |