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Serum Myostatin Is Reduced in Individuals with Metabolic Syndrome
AIMS: Myostatin is a negative regulator of skeletal muscle mass and may also modulate energy metabolism secondarily. We aim to investigate the relationship between serum myostatin and the metabolic variables in diabetic (DM) and non-diabetic subjects. MATERIALS AND METHODS: A cross-sectional study r...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177900/ https://www.ncbi.nlm.nih.gov/pubmed/25254550 http://dx.doi.org/10.1371/journal.pone.0108230 |
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author | Han, Der-Sheng Chu-Su, Yu Chiang, Chih-Kang Tseng, Fen-Yu Tseng, Ping-Huei Chen, Chi-Ling Wu, Kwan-Dun Yang, Wei-Shiung |
author_facet | Han, Der-Sheng Chu-Su, Yu Chiang, Chih-Kang Tseng, Fen-Yu Tseng, Ping-Huei Chen, Chi-Ling Wu, Kwan-Dun Yang, Wei-Shiung |
author_sort | Han, Der-Sheng |
collection | PubMed |
description | AIMS: Myostatin is a negative regulator of skeletal muscle mass and may also modulate energy metabolism secondarily. We aim to investigate the relationship between serum myostatin and the metabolic variables in diabetic (DM) and non-diabetic subjects. MATERIALS AND METHODS: A cross-sectional study recruiting 246 consecutive DM patients and 82 age- and gender-matched non-diabetic individuals at a medical center was conducted. The variables of anthropometry and blood chemistry were obtained. Serum myostatin level was measured with enzyme immunoassay. RESULTS: DM group had lower serum myostatin compared with non-diabetics (7.82 versus 9.28 ng/ml, p<0.01). Sixty-two percent of the recruited individuals had metabolic syndrome (MetS). The patients with MetS had significantly lower serum myostatin than those without (7.39 versus 9.49 ng/ml, p<0.001). The serum myostatin level decreased with increasing numbers of the MetS components (p for trend<0.001). The patients with higher body mass index, larger abdominal girth, lower high-density lipoprotein cholesterol (HDL-C), and higher triglycerides had lower serum myostatin than those without. The serum myostatin level was independently negatively related to larger abdominal girth, higher triglycerides, and lower HDL-C after adjustment. The odds ratios for MetS, central obesity, low HDL-C, high triglycerides, and DM were 0.85, 0.88, 0.89, 0.85, and 0.92, respectively, when serum myostatin increased per 1 ng/mL, in the binary logistic regression models. CONCLUSIONS: Lower serum myostatin independently associated with MetS, central obesity, low HDL-C, and high triglycerides after adjustment. Higher serum myostatin is associated with favorable metabolic profiles. |
format | Online Article Text |
id | pubmed-4177900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41779002014-10-02 Serum Myostatin Is Reduced in Individuals with Metabolic Syndrome Han, Der-Sheng Chu-Su, Yu Chiang, Chih-Kang Tseng, Fen-Yu Tseng, Ping-Huei Chen, Chi-Ling Wu, Kwan-Dun Yang, Wei-Shiung PLoS One Research Article AIMS: Myostatin is a negative regulator of skeletal muscle mass and may also modulate energy metabolism secondarily. We aim to investigate the relationship between serum myostatin and the metabolic variables in diabetic (DM) and non-diabetic subjects. MATERIALS AND METHODS: A cross-sectional study recruiting 246 consecutive DM patients and 82 age- and gender-matched non-diabetic individuals at a medical center was conducted. The variables of anthropometry and blood chemistry were obtained. Serum myostatin level was measured with enzyme immunoassay. RESULTS: DM group had lower serum myostatin compared with non-diabetics (7.82 versus 9.28 ng/ml, p<0.01). Sixty-two percent of the recruited individuals had metabolic syndrome (MetS). The patients with MetS had significantly lower serum myostatin than those without (7.39 versus 9.49 ng/ml, p<0.001). The serum myostatin level decreased with increasing numbers of the MetS components (p for trend<0.001). The patients with higher body mass index, larger abdominal girth, lower high-density lipoprotein cholesterol (HDL-C), and higher triglycerides had lower serum myostatin than those without. The serum myostatin level was independently negatively related to larger abdominal girth, higher triglycerides, and lower HDL-C after adjustment. The odds ratios for MetS, central obesity, low HDL-C, high triglycerides, and DM were 0.85, 0.88, 0.89, 0.85, and 0.92, respectively, when serum myostatin increased per 1 ng/mL, in the binary logistic regression models. CONCLUSIONS: Lower serum myostatin independently associated with MetS, central obesity, low HDL-C, and high triglycerides after adjustment. Higher serum myostatin is associated with favorable metabolic profiles. Public Library of Science 2014-09-25 /pmc/articles/PMC4177900/ /pubmed/25254550 http://dx.doi.org/10.1371/journal.pone.0108230 Text en © 2014 Han et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Han, Der-Sheng Chu-Su, Yu Chiang, Chih-Kang Tseng, Fen-Yu Tseng, Ping-Huei Chen, Chi-Ling Wu, Kwan-Dun Yang, Wei-Shiung Serum Myostatin Is Reduced in Individuals with Metabolic Syndrome |
title | Serum Myostatin Is Reduced in Individuals with Metabolic Syndrome |
title_full | Serum Myostatin Is Reduced in Individuals with Metabolic Syndrome |
title_fullStr | Serum Myostatin Is Reduced in Individuals with Metabolic Syndrome |
title_full_unstemmed | Serum Myostatin Is Reduced in Individuals with Metabolic Syndrome |
title_short | Serum Myostatin Is Reduced in Individuals with Metabolic Syndrome |
title_sort | serum myostatin is reduced in individuals with metabolic syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177900/ https://www.ncbi.nlm.nih.gov/pubmed/25254550 http://dx.doi.org/10.1371/journal.pone.0108230 |
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