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Reduction in Endogenous Insulin Secretion is a Risk Factor of Sarcopenia in Men with Type 2 Diabetes Mellitus

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Abstract

Sarcopenia has recently attracted widespread attention, because it increases risks of fall and bedridden. Although patients with type 2 diabetes mellitus (T2DM) are known to have lower muscle mass of limbs than healthy people, the mechanism is still unclear. We thus examined the association of muscle mass with parameters of endogenous insulin secretion such as fasting immunoreactive insulin, fasting C-peptide immunoreactivity (CPR), and daily urine CPR in 191 men with T2DM. Muscle mass of arms and legs was evaluated by dual-energy X-ray absorptiometry, and we calculated relative skeletal muscle index (RSMI), which is useful for the diagnosis of sarcopenia. Multiple regression analyses adjusted for age, duration of T2DM, serum creatinine, HbA1c, and insulin-like growth factor-I showed that each parameter of endogenous insulin was significantly and positively correlated with muscle mass of arms and legs as well as RSMI (p < 0.05). Moreover, logistic regression analyses adjusted for confounding factors mentioned above showed that each parameter of endogenous insulin was significantly lower in subjects with sarcopenia than those without it (p < 0.05). In conclusion, reduction in endogenous insulin secretion is an independent risk factor of sarcopenia in men with T2DM.

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Conflict of interest

All authors Ken-ichiro Tanaka, Ippei Kanazawa, and Toshitsugu Sugimoto have any conflict of interest.

Human and Animal Rights and Informed Consent

All subjects agreed to participate in this study and gave informed consent. This study was approved by the institutional review board of Shimane University Faculty of Medicine and complied with the Helsinki declaration.

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Correspondence to Ippei Kanazawa.

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Tanaka, Ki., Kanazawa, I. & Sugimoto, T. Reduction in Endogenous Insulin Secretion is a Risk Factor of Sarcopenia in Men with Type 2 Diabetes Mellitus. Calcif Tissue Int 97, 385–390 (2015). https://doi.org/10.1007/s00223-015-9990-8

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  • DOI: https://doi.org/10.1007/s00223-015-9990-8

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