Sarcopenia is an age-related loss of skeletal muscle mass, strength, and function that causes various health problems. In contrast, late-onset primary myopathies, which occur in the older population, are caused by a variety of factors, including genetic mutations, autoimmune processes, and metabolic abnormalities. Although sarcopenia and primary myopathy are two distinct disease processes, their symptoms can overlap, making differentiation challenging. The diagnostic criteria for sarcopenia have evolved over time, and various criteria have been proposed by expert groups. Late-onset primary muscle diseases such as inclusion body myositis, sporadic late-onset nemaline myopathy, muscular dystrophies, distal myopathies, myofibrillar myopathies, metabolic myopathies, and mitochondrial myopathies share common pathogenic mechanisms with sarcopenia, further complicating the diagnostic process. Appropriate clinical evaluation, including detailed history-taking, physical examination, and diagnostic testing, is essential for accurate diagnosis and management. Treatment approaches, including exercise, nutritional support, and disease-specific therapies, must be tailored to the characteristics of each disease. Despite these differences, sarcopenia and primary myopathies require careful consideration in the clinical setting for proper diagnosis and management. This review outlines the evolution of diagnostic criteria and diagnostic items for sarcopenia, late-onset primary myopathies that should be differentiated from sarcopenia, common pathomechanisms, and diagnostic algorithms to properly differentiate primary myopathies. Geriatr Gerontol Int 2024; 24: 1099–1110.
肌肉疏松症是一种与年龄有关的骨骼肌质量、力量和功能的丧失,会导致各种健康问题。相比之下,发生在老年人群中的晚发性原发性肌病由多种因素引起,包括基因突变、自身免疫过程和代谢异常。虽然肌肉疏松症和原发性肌病是两种不同的疾病过程,但它们的症状可能会重叠,因此很难区分。随着时间的推移,肌肉疏松症的诊断标准也在不断演变,专家组提出了各种不同的标准。晚发性原发性肌肉疾病,如包涵体肌炎、散发性晚发性神经性肌病、肌肉营养不良症、远端肌病、肌纤维肌病、代谢性肌病和线粒体肌病与肌少症有着共同的致病机制,使诊断过程更加复杂。适当的临床评估,包括详细的病史采集、体格检查和诊断测试,对于准确诊断和治疗至关重要。治疗方法,包括运动、营养支持和特定疾病疗法,都必须针对每种疾病的特点。尽管存在这些差异,肌少症和原发性肌病仍需要在临床环境中仔细考虑,以进行正确的诊断和管理。本综述概述了肌肉疏松症诊断标准和诊断项目的演变、应与肌肉疏松症区分开来的晚发性原发性肌病、常见的病理机制以及正确区分原发性肌病的诊断算法。Geriatr Gerontol Int 2024; --:-----.
{"title":"Late-onset primary muscle diseases mimicking sarcopenia","authors":"Satoshi Yamashita","doi":"10.1111/ggi.15000","DOIUrl":"10.1111/ggi.15000","url":null,"abstract":"<p>Sarcopenia is an age-related loss of skeletal muscle mass, strength, and function that causes various health problems. In contrast, late-onset primary myopathies, which occur in the older population, are caused by a variety of factors, including genetic mutations, autoimmune processes, and metabolic abnormalities. Although sarcopenia and primary myopathy are two distinct disease processes, their symptoms can overlap, making differentiation challenging. The diagnostic criteria for sarcopenia have evolved over time, and various criteria have been proposed by expert groups. Late-onset primary muscle diseases such as inclusion body myositis, sporadic late-onset nemaline myopathy, muscular dystrophies, distal myopathies, myofibrillar myopathies, metabolic myopathies, and mitochondrial myopathies share common pathogenic mechanisms with sarcopenia, further complicating the diagnostic process. Appropriate clinical evaluation, including detailed history-taking, physical examination, and diagnostic testing, is essential for accurate diagnosis and management. Treatment approaches, including exercise, nutritional support, and disease-specific therapies, must be tailored to the characteristics of each disease. Despite these differences, sarcopenia and primary myopathies require careful consideration in the clinical setting for proper diagnosis and management. This review outlines the evolution of diagnostic criteria and diagnostic items for sarcopenia, late-onset primary myopathies that should be differentiated from sarcopenia, common pathomechanisms, and diagnostic algorithms to properly differentiate primary myopathies. <b>Geriatr Gerontol Int 2024; 24: 1099–1110</b>.</p>","PeriodicalId":12546,"journal":{"name":"Geriatrics & Gerontology International","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142462643","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}