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Association between asymmetric dimethylarginine and sarcopenia in community-dwelling older women

Asymmetric dimethylarginine (ADMA) is an endogenous inhibitor of endothelium nitric oxide synthesis and causes endothelial dysfunction that may be related to sarcopenia. However, the association between ADMA and sarcopenia has not been studied. We evaluated the correlations between plasma ADMA level...

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Autores principales: Yokoro, Miyuki, Otaki, Naoto, Yano, Megumu, Imamura, Tomomi, Tanino, Norikazu, Fukuo, Keisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073180/
https://www.ncbi.nlm.nih.gov/pubmed/37015998
http://dx.doi.org/10.1038/s41598-023-32046-0
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author Yokoro, Miyuki
Otaki, Naoto
Yano, Megumu
Imamura, Tomomi
Tanino, Norikazu
Fukuo, Keisuke
author_facet Yokoro, Miyuki
Otaki, Naoto
Yano, Megumu
Imamura, Tomomi
Tanino, Norikazu
Fukuo, Keisuke
author_sort Yokoro, Miyuki
collection PubMed
description Asymmetric dimethylarginine (ADMA) is an endogenous inhibitor of endothelium nitric oxide synthesis and causes endothelial dysfunction that may be related to sarcopenia. However, the association between ADMA and sarcopenia has not been studied. We evaluated the correlations between plasma ADMA levels and sarcopenia in community-dwelling older women. In total, 144 community-dwelling older women participated in this study. Plasma ADMA levels were measured using a competitive enzyme-linked immunosorbent assay. Skeletal muscle mass, measured in terms of bioimpedance and grip strength, was used to assess sarcopenia. Plasma ADMA levels were significantly higher in participants with sarcopenia than in those without sarcopenia. Through receiver-operating characteristic curve analysis, the cutoff value of plasma ADMA level for sarcopenia was estimated at 0.57 μM. Sarcopenia was significantly more prevalent in participants with higher plasma ADMA levels than in those with lower plasma ADMA levels. According to logistic regression analysis, the crude odds ratio of higher plasma ADMA levels in participants with sarcopenia was 4.57 (95% confidence interval, 1.82–11.47; p = 0.001). Reductions in the skeletal muscle mass index over 2 years were significantly greater in participants with higher plasma ADMA levels. In conclusion, plasma ADMA levels were significantly associated with sarcopenia in community-dwelling older women.
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spelling pubmed-100731802023-04-06 Association between asymmetric dimethylarginine and sarcopenia in community-dwelling older women Yokoro, Miyuki Otaki, Naoto Yano, Megumu Imamura, Tomomi Tanino, Norikazu Fukuo, Keisuke Sci Rep Article Asymmetric dimethylarginine (ADMA) is an endogenous inhibitor of endothelium nitric oxide synthesis and causes endothelial dysfunction that may be related to sarcopenia. However, the association between ADMA and sarcopenia has not been studied. We evaluated the correlations between plasma ADMA levels and sarcopenia in community-dwelling older women. In total, 144 community-dwelling older women participated in this study. Plasma ADMA levels were measured using a competitive enzyme-linked immunosorbent assay. Skeletal muscle mass, measured in terms of bioimpedance and grip strength, was used to assess sarcopenia. Plasma ADMA levels were significantly higher in participants with sarcopenia than in those without sarcopenia. Through receiver-operating characteristic curve analysis, the cutoff value of plasma ADMA level for sarcopenia was estimated at 0.57 μM. Sarcopenia was significantly more prevalent in participants with higher plasma ADMA levels than in those with lower plasma ADMA levels. According to logistic regression analysis, the crude odds ratio of higher plasma ADMA levels in participants with sarcopenia was 4.57 (95% confidence interval, 1.82–11.47; p = 0.001). Reductions in the skeletal muscle mass index over 2 years were significantly greater in participants with higher plasma ADMA levels. In conclusion, plasma ADMA levels were significantly associated with sarcopenia in community-dwelling older women. Nature Publishing Group UK 2023-04-04 /pmc/articles/PMC10073180/ /pubmed/37015998 http://dx.doi.org/10.1038/s41598-023-32046-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Yokoro, Miyuki
Otaki, Naoto
Yano, Megumu
Imamura, Tomomi
Tanino, Norikazu
Fukuo, Keisuke
Association between asymmetric dimethylarginine and sarcopenia in community-dwelling older women
title Association between asymmetric dimethylarginine and sarcopenia in community-dwelling older women
title_full Association between asymmetric dimethylarginine and sarcopenia in community-dwelling older women
title_fullStr Association between asymmetric dimethylarginine and sarcopenia in community-dwelling older women
title_full_unstemmed Association between asymmetric dimethylarginine and sarcopenia in community-dwelling older women
title_short Association between asymmetric dimethylarginine and sarcopenia in community-dwelling older women
title_sort association between asymmetric dimethylarginine and sarcopenia in community-dwelling older women
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073180/
https://www.ncbi.nlm.nih.gov/pubmed/37015998
http://dx.doi.org/10.1038/s41598-023-32046-0
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