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Myostatin and markers of bone metabolism in dermatomyositis
BACKGROUND: In dermatomyostis (DM) patients, inflammation, reduced activity, and medication have a negative impact on the musculoskeletal system. Several endocrine factors are involved in muscle growth and bone turnover. Objective: We aimed to investigate factors regulating myogenesis and bone metab...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866468/ https://www.ncbi.nlm.nih.gov/pubmed/33546660 http://dx.doi.org/10.1186/s12891-021-04030-0 |
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author | Kerschan-Schindl, Katharina Gruther, Wolfgang Föger-Samwald, Ursula Bangert, Christine Kudlacek, Stefan Pietschmann, Peter |
author_facet | Kerschan-Schindl, Katharina Gruther, Wolfgang Föger-Samwald, Ursula Bangert, Christine Kudlacek, Stefan Pietschmann, Peter |
author_sort | Kerschan-Schindl, Katharina |
collection | PubMed |
description | BACKGROUND: In dermatomyostis (DM) patients, inflammation, reduced activity, and medication have a negative impact on the musculoskeletal system. Several endocrine factors are involved in muscle growth and bone turnover. Objective: We aimed to investigate factors regulating myogenesis and bone metabolism and to evaluate possible associations between these endocrine factors, muscle strength, and functional tests in DM patients. METHODS: We conducted a cross-sectional study in 20 dermatomyositis patients. Serum levels of myostatin (MSTN), follistatin (FSTN), dickkopf 1 (Dkk1), sclerostin (SOST), periostin (PSTN), the receptor activator nuclear factor kB ligand (RANKL):osteoprotegerin (OPG) ratio and fibroblast growth factor 23 (FGF23) were determined. Physical function was evaluated by hand-held strength measurement, chair rising test, timed up and go test and the 3-min walking test. RESULTS: Serum MSTN and FGF23 levels (2.5 [1.9; 3.2] vs. 1.9 [1.6; 2.3] and 2.17 [1.45; 3.26] vs. 1.28 [0.79; 1.96], respectively; p < 0.05) were significantly higher in DM patients than in controls. Dkk1 was significantly lower (11.4 [6.9; 20.0] vs. 31.8 [14.3; 50.6], p < 0.01). Muscle strength and physical function tests correlated with each other (e.g. hip flexion – timed up and go test: r = − 0.748, p < 0.01). CONCLUSION: In DM patients, biochemical musculo-skeletal markers are altered and physical function shows deficits. All these tests reflect independent of each other different deficits in long-term DM patients which is important for the assessment of DM patients as well as planning of therapeutic interventions in clinical routine. |
format | Online Article Text |
id | pubmed-7866468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78664682021-02-08 Myostatin and markers of bone metabolism in dermatomyositis Kerschan-Schindl, Katharina Gruther, Wolfgang Föger-Samwald, Ursula Bangert, Christine Kudlacek, Stefan Pietschmann, Peter BMC Musculoskelet Disord Research Article BACKGROUND: In dermatomyostis (DM) patients, inflammation, reduced activity, and medication have a negative impact on the musculoskeletal system. Several endocrine factors are involved in muscle growth and bone turnover. Objective: We aimed to investigate factors regulating myogenesis and bone metabolism and to evaluate possible associations between these endocrine factors, muscle strength, and functional tests in DM patients. METHODS: We conducted a cross-sectional study in 20 dermatomyositis patients. Serum levels of myostatin (MSTN), follistatin (FSTN), dickkopf 1 (Dkk1), sclerostin (SOST), periostin (PSTN), the receptor activator nuclear factor kB ligand (RANKL):osteoprotegerin (OPG) ratio and fibroblast growth factor 23 (FGF23) were determined. Physical function was evaluated by hand-held strength measurement, chair rising test, timed up and go test and the 3-min walking test. RESULTS: Serum MSTN and FGF23 levels (2.5 [1.9; 3.2] vs. 1.9 [1.6; 2.3] and 2.17 [1.45; 3.26] vs. 1.28 [0.79; 1.96], respectively; p < 0.05) were significantly higher in DM patients than in controls. Dkk1 was significantly lower (11.4 [6.9; 20.0] vs. 31.8 [14.3; 50.6], p < 0.01). Muscle strength and physical function tests correlated with each other (e.g. hip flexion – timed up and go test: r = − 0.748, p < 0.01). CONCLUSION: In DM patients, biochemical musculo-skeletal markers are altered and physical function shows deficits. All these tests reflect independent of each other different deficits in long-term DM patients which is important for the assessment of DM patients as well as planning of therapeutic interventions in clinical routine. BioMed Central 2021-02-05 /pmc/articles/PMC7866468/ /pubmed/33546660 http://dx.doi.org/10.1186/s12891-021-04030-0 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article Kerschan-Schindl, Katharina Gruther, Wolfgang Föger-Samwald, Ursula Bangert, Christine Kudlacek, Stefan Pietschmann, Peter Myostatin and markers of bone metabolism in dermatomyositis |
title | Myostatin and markers of bone metabolism in dermatomyositis |
title_full | Myostatin and markers of bone metabolism in dermatomyositis |
title_fullStr | Myostatin and markers of bone metabolism in dermatomyositis |
title_full_unstemmed | Myostatin and markers of bone metabolism in dermatomyositis |
title_short | Myostatin and markers of bone metabolism in dermatomyositis |
title_sort | myostatin and markers of bone metabolism in dermatomyositis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866468/ https://www.ncbi.nlm.nih.gov/pubmed/33546660 http://dx.doi.org/10.1186/s12891-021-04030-0 |
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