糖尿病性肌肉疏松症。糖尿病患者肌肉筛查方案建议

Daniel de Luis Román, Juana Carretero Gómez, José Manuel García-Almeida, Fernando Garrachón Vallo, German Guzmán Rolo, Juan José López Gómez, Francisco José Tarazona-Santabalbina, Alejandro Sanz-Paris
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引用次数: 0

摘要

目的 提出 "糖尿病肌肉疏松症 "作为糖尿病新合并症的依据,并建立肌肉筛查算法建议,以便在临床实践中对其进行诊断和分期。研究方法采用名义技术进行专家意见定性研究。以 "筛查 "或 "诊断标准"、"肌肉损失 "或 "肌肉疏松症 "和 "糖尿病 "为关键词进行文献检索,并将检索结果发送给由 7 位专家组成的多学科小组,他们在面对面的会议上讨论了筛查算法的各个方面。结果:糖尿病性肌肉疏松症(DS)的特征是糖尿病(DM)患者特有的肌肉质量萎缩,与组织学和生理学上正常的肌肉质量截然不同。筛查的目标人群被定义为 SARC-F 问卷调查结果为 4、糖化血红蛋白(HbA1C)≥ 8.0%、患糖尿病超过 5 年、服用磺脲类、格列奈类和钠/葡萄糖共转运抑制剂(SGLT2)、有糖尿病慢性并发症或临床怀疑患有肌肉疏松症的糖尿病患者。诊断的依据是是否存在肌力低下(可能患有肌肉疏松症)和肌肉质量低下(确诊患有肌肉疏松症)的标准,使用的方法可在任何临床诊室找到,例如测力法、椅子站立测试和体重指数(BMI)调整后的小腿围。DS 被分为 4 个阶段:I 期为无其他糖尿病并发症的肌无力患者,II 期为有某种糖尿病并发症的患者。II 期中又分为三个次级(a、b 和 c)。IIa 期指患有肌肉疏松性糖尿病并伴有某些糖尿病特异性损伤的患者,IIb 期指患有肌肉疏松性疾病并伴有功能损伤的患者,IIc 期指患有糖尿病并发症并使用标准测试测量功能变化的肌肉疏松性疾病患者:糖尿病性肌肉疏松症对 2 型糖尿病(T2DM)患者的功能和生活质量有重大影响,因此必须像传统上描述的所有其他 T2DM 并发症一样给予同等重视。本文件旨在为糖尿病肌肉疏松症的筛查和诊断规范化奠定基础,其方式简单易行,便于各级医疗机构使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Diabetic Sarcopenia. A proposed muscle screening protocol in people with diabetes

Diabetic Sarcopenia. A proposed muscle screening protocol in people with diabetes

Objectives

To propose the grounds for “diabetic sarcopenia” as a new comorbidity of diabetes, and to establish a muscle screening algorithm proposal to facilitate its diagnosis and staging in clinical practice. Method: A qualitative expert opinion study was carried out using the nominal technique. A literature search was performed with the terms “screening” or “diagnostic criteria” and “muscle loss” or “sarcopenia” and “diabetes” that was sent to a multidisciplinary group of 7 experts who, in a face-to-face meeting, discussed various aspects of the screening algorithm. Results: The hallmark of diabetic sarcopenia (DS) is muscle mass atrophy characteristic of people with diabetes mellitus (DM) in contrast to the histological and physiological normality of muscle mass. The target population to be screened was defined as patients with DM with a SARC-F questionnaire > 4, glycosylated haemoglobin (HbA1C) ≥ 8.0%, more than 5 years since onset of DM, taking sulfonylureas, glinides and sodium/glucose cotransporter inhibitors (SGLT2), as well as presence of chronic complications of diabetes or clinical suspicion of sarcopenia. Diagnosis was based on the presence of criteria of low muscle strength (probable sarcopenia) and low muscle mass (confirmed sarcopenia) using methods available in any clinical consultation room, such as dynamometry, the chair stand test, and Body Mass Index (BMI)-adjusted calf circumference. DS was classified into 4 stages: Stage I corresponds to sarcopenic patients with no other diabetes complication, and Stage II corresponds to patients with some type of involvement. Within Stage II are three sublevels (a, b and c). Stage IIa refers to individuals with sarcopenic diabetes and some diabetes-specific impairment, IIb to sarcopenia with functional impairment, and IIc to sarcopenia with diabetes complications and changes in function measured using standard tests Conclusion: Diabetic sarcopenia has a significant impact on function and quality of life in people with type 2 diabetes mellitus (T2DM), and it is important to give it the same attention as all other traditionally described complications of T2DM. This document aims to establish the foundation for protocolising the screening and diagnosis of diabetic sarcopenia in a manner that is simple and accessible for all levels of healthcare.

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