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Low skeletal muscle mass is associated with the risk of all-cause mortality in patients with type 2 diabetes mellitus
BACKGROUND: Patients with type 2 diabetes mellitus (T2DM) have an increased risk of muscle mass reduction. However, the association between muscle mass and mortality in T2DM remains unknown. METHODS: This was a historical cohort study with the endpoint of all-cause mortality. This study included 163...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477760/ https://www.ncbi.nlm.nih.gov/pubmed/31040938 http://dx.doi.org/10.1177/2042018819842971 |
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author | Miyake, Hitomi Kanazawa, Ippei Tanaka, Ken-ichiro Sugimoto, Toshitsugu |
author_facet | Miyake, Hitomi Kanazawa, Ippei Tanaka, Ken-ichiro Sugimoto, Toshitsugu |
author_sort | Miyake, Hitomi |
collection | PubMed |
description | BACKGROUND: Patients with type 2 diabetes mellitus (T2DM) have an increased risk of muscle mass reduction. However, the association between muscle mass and mortality in T2DM remains unknown. METHODS: This was a historical cohort study with the endpoint of all-cause mortality. This study included 163 Japanese men and 141 postmenopausal women with T2DM whose body compositions were evaluated using dual-energy X-ray absorptiometry. Low muscle mass was defined as a skeletal muscle mass index (SMI) of <7.0 kg/m(2) for men and <5.4 kg/m(2) for women. RESULTS: During the 6-year follow-up period, 32 men and 14 women died. In a Cox regression analysis adjusted for age, T2DM duration, glycated hemoglobin, serum creatinine, fasting C-peptide, body mass index, and lean body mass were associated with the risk of mortality in men [hazard ratio (HR) = 1.81, 95% confidence interval (CI) = 1.00–3.28 per standard deviation (SD) decrease, p = 0.049] and women (HR = 4.53, 95% CI = 1.14–17.96 per SD decrease, p = 0.032). Neither fat mass nor bone mineral content was associated with mortality. Low SMI was associated with increased mortality in women (HR = 5.97, 95% CI = 1.04–34.37, p = 0.045), while the association between low SMI and mortality was marginal in men (HR = 2.38, 95% CI = 0.92–6.14, p = 0.074). CONCLUSIONS: Low muscle mass was independently associated with all-cause mortality in patients with T2DM. The preservation of skeletal muscle mass is important to protect patients with T2DM from increased mortality risk. |
format | Online Article Text |
id | pubmed-6477760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-64777602019-04-30 Low skeletal muscle mass is associated with the risk of all-cause mortality in patients with type 2 diabetes mellitus Miyake, Hitomi Kanazawa, Ippei Tanaka, Ken-ichiro Sugimoto, Toshitsugu Ther Adv Endocrinol Metab Original Research BACKGROUND: Patients with type 2 diabetes mellitus (T2DM) have an increased risk of muscle mass reduction. However, the association between muscle mass and mortality in T2DM remains unknown. METHODS: This was a historical cohort study with the endpoint of all-cause mortality. This study included 163 Japanese men and 141 postmenopausal women with T2DM whose body compositions were evaluated using dual-energy X-ray absorptiometry. Low muscle mass was defined as a skeletal muscle mass index (SMI) of <7.0 kg/m(2) for men and <5.4 kg/m(2) for women. RESULTS: During the 6-year follow-up period, 32 men and 14 women died. In a Cox regression analysis adjusted for age, T2DM duration, glycated hemoglobin, serum creatinine, fasting C-peptide, body mass index, and lean body mass were associated with the risk of mortality in men [hazard ratio (HR) = 1.81, 95% confidence interval (CI) = 1.00–3.28 per standard deviation (SD) decrease, p = 0.049] and women (HR = 4.53, 95% CI = 1.14–17.96 per SD decrease, p = 0.032). Neither fat mass nor bone mineral content was associated with mortality. Low SMI was associated with increased mortality in women (HR = 5.97, 95% CI = 1.04–34.37, p = 0.045), while the association between low SMI and mortality was marginal in men (HR = 2.38, 95% CI = 0.92–6.14, p = 0.074). CONCLUSIONS: Low muscle mass was independently associated with all-cause mortality in patients with T2DM. The preservation of skeletal muscle mass is important to protect patients with T2DM from increased mortality risk. SAGE Publications 2019-04-22 /pmc/articles/PMC6477760/ /pubmed/31040938 http://dx.doi.org/10.1177/2042018819842971 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Miyake, Hitomi Kanazawa, Ippei Tanaka, Ken-ichiro Sugimoto, Toshitsugu Low skeletal muscle mass is associated with the risk of all-cause mortality in patients with type 2 diabetes mellitus |
title | Low skeletal muscle mass is associated with the risk of all-cause
mortality in patients with type 2 diabetes mellitus |
title_full | Low skeletal muscle mass is associated with the risk of all-cause
mortality in patients with type 2 diabetes mellitus |
title_fullStr | Low skeletal muscle mass is associated with the risk of all-cause
mortality in patients with type 2 diabetes mellitus |
title_full_unstemmed | Low skeletal muscle mass is associated with the risk of all-cause
mortality in patients with type 2 diabetes mellitus |
title_short | Low skeletal muscle mass is associated with the risk of all-cause
mortality in patients with type 2 diabetes mellitus |
title_sort | low skeletal muscle mass is associated with the risk of all-cause
mortality in patients with type 2 diabetes mellitus |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477760/ https://www.ncbi.nlm.nih.gov/pubmed/31040938 http://dx.doi.org/10.1177/2042018819842971 |
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