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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...

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Autores principales: Bouchi, Ryotaro, Fukuda, Tatsuya, Takeuchi, Takato, Nakano, Yujiro, Murakami, Masanori, Minami, Isao, Izumiyama, Hajime, Hashimoto, Koshi, Yoshimoto, Takanobu, Ogawa, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
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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.
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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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