de Luis Román Daniel, Gómez Juana Carretero, García-Almeida José Manuel, Vallo Fernando Garrachón, Rolo German Guzmán, Gómez Juan José López, Tarazona-Santabalbina Francisco José, Sanz-Paris Alejandro
Center Investigación of Endocrinology and Nutrition, University of Valladolid, Valladolid, Spain.
Internal Medicine Department, University Hospital of Badajoz, Badajoz, Spain.
Rev Endocr Metab Disord. 2024 Aug;25(4):651-661. doi: 10.1007/s11154-023-09871-9. Epub 2024 Feb 5.
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.
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.
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.
提出将“糖尿病性肌肉减少症”作为糖尿病一种新的合并症的依据,并建立一种肌肉筛查算法建议,以促进其在临床实践中的诊断和分期。
采用名义小组技术进行了一项定性专家意见研究。使用“筛查”或“诊断标准”以及“肌肉减少”或“肌肉减少症”和“糖尿病”等术语进行文献检索,并将检索结果发送给一个由7名专家组成的多学科小组,这些专家在一次面对面会议上讨论了筛查算法的各个方面。
糖尿病性肌肉减少症(DS)的标志是与肌肉量的组织学和生理正常情况相比,糖尿病患者特有的肌肉量萎缩。筛查的目标人群定义为SARC-F问卷得分>4、糖化血红蛋白(HbA1C)≥8.0%、糖尿病发病超过5年、正在服用磺脲类药物、格列奈类药物和钠/葡萄糖协同转运蛋白抑制剂(SGLT2),以及存在糖尿病慢性并发症或临床怀疑有肌肉减少症的糖尿病患者。诊断基于使用任何临床诊室都可用的方法,如握力测量、椅子站立试验和体重指数(BMI)校正后的小腿围,存在低肌肉力量标准(可能的肌肉减少症)和低肌肉量标准(确诊的肌肉减少症)。DS分为4个阶段:I期对应无其他糖尿病并发症的肌肉减少症患者,II期对应有某种类型受累的患者。在II期内有三个子阶段(a、b和c)。IIa期指患有肌肉减少性糖尿病和某些糖尿病特异性损害的个体,IIb期指伴有功能损害的肌肉减少症,IIc期指伴有糖尿病并发症且使用标准测试测量功能有变化的肌肉减少症。结论:糖尿病性肌肉减少症对2型糖尿病(T2DM)患者的功能和生活质量有重大影响,与T2DM所有其他传统描述的并发症一样重视它很重要。本文档旨在为以一种对各级医疗保健都简单易懂的方式规范糖尿病性肌肉减少症的筛查和诊断奠定基础。