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Insulin Treatment Attenuates Decline of Muscle Mass in Japanese Patients with Type 2 Diabetes
Sarcopenia is defined as an age-related loss of skeletal muscle mass and strength, and is a major cause of disability and mobility limitations. Recent studies have demonstrated that type 2 diabetes and insulin signaling deficiencies contribute to the progression of sarcopenia, suggesting that a suff...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486921/ https://www.ncbi.nlm.nih.gov/pubmed/28246927 http://dx.doi.org/10.1007/s00223-017-0251-x |
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author | Bouchi, Ryotaro Fukuda, Tatsuya Takeuchi, Takato Nakano, Yujiro Murakami, Masanori Minami, Isao Izumiyama, Hajime Hashimoto, Koshi Yoshimoto, Takanobu Ogawa, Yoshihiro |
author_facet | Bouchi, Ryotaro Fukuda, Tatsuya Takeuchi, Takato Nakano, Yujiro Murakami, Masanori Minami, Isao Izumiyama, Hajime Hashimoto, Koshi Yoshimoto, Takanobu Ogawa, Yoshihiro |
author_sort | Bouchi, Ryotaro |
collection | PubMed |
description | Sarcopenia is defined as an age-related loss of skeletal muscle mass and strength, and is a major cause of disability and mobility limitations. Recent studies have demonstrated that type 2 diabetes and insulin signaling deficiencies contribute to the progression of sarcopenia, suggesting that a sufficient supply of insulin to the skeletal muscles may be important for the maintenance of muscle function; however, little has been reported regarding whether insulin treatment can protect against sarcopenia. We conducted a retrospective observational study to examine the impact of insulin treatment on the muscle mass of patients with type 2 diabetes. A total of 312 patients (mean age: 64 ± 11 years; 40.8% female; 27.6% treated with insulin) were studied in this retrospective observational study. Skeletal muscle index (SMI) and grip strength (kg) were used to assess sarcopenia. The prevalence of sarcopenia was 18.0%. Insulin treatment was shown to be protective against the annual decline of SMI (standardized β 0.195; p = 0.025) even after adjusting for covariates, including age, gender, duration of diabetes, and body mass index. In a cohort matched by propensity scores, insulin treatment significantly increased the 1-year change in SMI (mean ± SE) compared with non-insulin-treated group (2.40 ± 0.98% vs. −0.43 ± 0.98%; p = 0.050). Our data suggest that insulin treatment could attenuate the progression of sarcopenia in patients with type 2 diabetes. |
format | Online Article Text |
id | pubmed-5486921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-54869212017-07-17 Insulin Treatment Attenuates Decline of Muscle Mass in Japanese Patients with Type 2 Diabetes Bouchi, Ryotaro Fukuda, Tatsuya Takeuchi, Takato Nakano, Yujiro Murakami, Masanori Minami, Isao Izumiyama, Hajime Hashimoto, Koshi Yoshimoto, Takanobu Ogawa, Yoshihiro Calcif Tissue Int Original Research Sarcopenia is defined as an age-related loss of skeletal muscle mass and strength, and is a major cause of disability and mobility limitations. Recent studies have demonstrated that type 2 diabetes and insulin signaling deficiencies contribute to the progression of sarcopenia, suggesting that a sufficient supply of insulin to the skeletal muscles may be important for the maintenance of muscle function; however, little has been reported regarding whether insulin treatment can protect against sarcopenia. We conducted a retrospective observational study to examine the impact of insulin treatment on the muscle mass of patients with type 2 diabetes. A total of 312 patients (mean age: 64 ± 11 years; 40.8% female; 27.6% treated with insulin) were studied in this retrospective observational study. Skeletal muscle index (SMI) and grip strength (kg) were used to assess sarcopenia. The prevalence of sarcopenia was 18.0%. Insulin treatment was shown to be protective against the annual decline of SMI (standardized β 0.195; p = 0.025) even after adjusting for covariates, including age, gender, duration of diabetes, and body mass index. In a cohort matched by propensity scores, insulin treatment significantly increased the 1-year change in SMI (mean ± SE) compared with non-insulin-treated group (2.40 ± 0.98% vs. −0.43 ± 0.98%; p = 0.050). Our data suggest that insulin treatment could attenuate the progression of sarcopenia in patients with type 2 diabetes. Springer US 2017-02-28 2017 /pmc/articles/PMC5486921/ /pubmed/28246927 http://dx.doi.org/10.1007/s00223-017-0251-x Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Bouchi, Ryotaro Fukuda, Tatsuya Takeuchi, Takato Nakano, Yujiro Murakami, Masanori Minami, Isao Izumiyama, Hajime Hashimoto, Koshi Yoshimoto, Takanobu Ogawa, Yoshihiro Insulin Treatment Attenuates Decline of Muscle Mass in Japanese Patients with Type 2 Diabetes |
title | Insulin Treatment Attenuates Decline of Muscle Mass in Japanese Patients with Type 2 Diabetes |
title_full | Insulin Treatment Attenuates Decline of Muscle Mass in Japanese Patients with Type 2 Diabetes |
title_fullStr | Insulin Treatment Attenuates Decline of Muscle Mass in Japanese Patients with Type 2 Diabetes |
title_full_unstemmed | Insulin Treatment Attenuates Decline of Muscle Mass in Japanese Patients with Type 2 Diabetes |
title_short | Insulin Treatment Attenuates Decline of Muscle Mass in Japanese Patients with Type 2 Diabetes |
title_sort | insulin treatment attenuates decline of muscle mass in japanese patients with type 2 diabetes |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486921/ https://www.ncbi.nlm.nih.gov/pubmed/28246927 http://dx.doi.org/10.1007/s00223-017-0251-x |
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