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Correlation between lower extremity arterial disease and skeletal muscle mass in patients with type 2 diabetes mellitus
OBJECTIVES: To evaluate skeletal muscle mass in patients with both type 2 diabetes mellitus (T2DM) and concomitant lower extremity arterial disease (LEAD) and determine the contribution of skeletal muscle mass to macrovascular diseases. METHODS: In total, 112 patients with T2DM were divided into the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282344/ https://www.ncbi.nlm.nih.gov/pubmed/32212874 http://dx.doi.org/10.1177/0300060519897483 |
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author | Zhang, Yinghui Ren, Lemeng Zheng, Fengjie Zhuang, Xianghua Jiang, Dongqing Chen, Shihong Ni, Yihong Li, Xiaobao |
author_facet | Zhang, Yinghui Ren, Lemeng Zheng, Fengjie Zhuang, Xianghua Jiang, Dongqing Chen, Shihong Ni, Yihong Li, Xiaobao |
author_sort | Zhang, Yinghui |
collection | PubMed |
description | OBJECTIVES: To evaluate skeletal muscle mass in patients with both type 2 diabetes mellitus (T2DM) and concomitant lower extremity arterial disease (LEAD) and determine the contribution of skeletal muscle mass to macrovascular diseases. METHODS: In total, 112 patients with T2DM were divided into the T2DM and T2DM + LEAD groups. Hepatic function, renal function, uric acid, blood glucose, and glycated hemoglobin (HbA1C) were measured. Dual-energy X-ray absorptiometry was used to measure visceral fat area and skeletal muscle mass index (SMI). RESULTS: Waist-to-hip ratio, uric acid, and body fat percentage were significantly higher in the T2DM+LEAD group than in the T2DM group; SMI was significantly lower in the T2DM+LEAD group than in the T2DM group. There were no significant differences in albumin, creatinine, fasting blood glucose, HbA1C, or blood lipids. Uric acid, SMI, and body fat percentage were significantly positively correlated with T2DM and concomitant LEAD. Logistic regression analyses suggested that SMI is an independent risk factor for LEAD in T2DM (odds ratio = 1.517; 95% confidence interval: 1.082–2.126). CONCLUSIONS: Skeletal muscle mass is lower in patients with T2DM and concomitant LEAD than in patients with T2DM who do not exhibit LEAD. SMI is an important risk factor for LEAD. |
format | Online Article Text |
id | pubmed-7282344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-72823442020-06-17 Correlation between lower extremity arterial disease and skeletal muscle mass in patients with type 2 diabetes mellitus Zhang, Yinghui Ren, Lemeng Zheng, Fengjie Zhuang, Xianghua Jiang, Dongqing Chen, Shihong Ni, Yihong Li, Xiaobao J Int Med Res Retrospective Clinical Research Report OBJECTIVES: To evaluate skeletal muscle mass in patients with both type 2 diabetes mellitus (T2DM) and concomitant lower extremity arterial disease (LEAD) and determine the contribution of skeletal muscle mass to macrovascular diseases. METHODS: In total, 112 patients with T2DM were divided into the T2DM and T2DM + LEAD groups. Hepatic function, renal function, uric acid, blood glucose, and glycated hemoglobin (HbA1C) were measured. Dual-energy X-ray absorptiometry was used to measure visceral fat area and skeletal muscle mass index (SMI). RESULTS: Waist-to-hip ratio, uric acid, and body fat percentage were significantly higher in the T2DM+LEAD group than in the T2DM group; SMI was significantly lower in the T2DM+LEAD group than in the T2DM group. There were no significant differences in albumin, creatinine, fasting blood glucose, HbA1C, or blood lipids. Uric acid, SMI, and body fat percentage were significantly positively correlated with T2DM and concomitant LEAD. Logistic regression analyses suggested that SMI is an independent risk factor for LEAD in T2DM (odds ratio = 1.517; 95% confidence interval: 1.082–2.126). CONCLUSIONS: Skeletal muscle mass is lower in patients with T2DM and concomitant LEAD than in patients with T2DM who do not exhibit LEAD. SMI is an important risk factor for LEAD. SAGE Publications 2020-03-25 /pmc/articles/PMC7282344/ /pubmed/32212874 http://dx.doi.org/10.1177/0300060519897483 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://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 | Retrospective Clinical Research Report Zhang, Yinghui Ren, Lemeng Zheng, Fengjie Zhuang, Xianghua Jiang, Dongqing Chen, Shihong Ni, Yihong Li, Xiaobao Correlation between lower extremity arterial disease and skeletal muscle mass in patients with type 2 diabetes mellitus |
title | Correlation between lower extremity arterial disease and skeletal muscle mass in patients with type 2 diabetes mellitus |
title_full | Correlation between lower extremity arterial disease and skeletal muscle mass in patients with type 2 diabetes mellitus |
title_fullStr | Correlation between lower extremity arterial disease and skeletal muscle mass in patients with type 2 diabetes mellitus |
title_full_unstemmed | Correlation between lower extremity arterial disease and skeletal muscle mass in patients with type 2 diabetes mellitus |
title_short | Correlation between lower extremity arterial disease and skeletal muscle mass in patients with type 2 diabetes mellitus |
title_sort | correlation between lower extremity arterial disease and skeletal muscle mass in patients with type 2 diabetes mellitus |
topic | Retrospective Clinical Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282344/ https://www.ncbi.nlm.nih.gov/pubmed/32212874 http://dx.doi.org/10.1177/0300060519897483 |
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