Diagnosing ALS: the Gold Coast criteria and the role of EMG

Journal article

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by the loss of motor neurons in the spinal cord and brain, resulting in motor deficits and muscle atrophy. Approximately 5–10% of ALS patients are familial (fALS), while the rest are sporadic (sALS). Currently, early diagnosis of ALS cannot be achieved based on clinical manifestations and electromyography due to the lack of effective and easily available biomarkers. The skin and central nervous system (CNS) share the same embryonic origin. Several skin biomarkers have been found in many neurodegenerative diseases, such as abnormal deposition of pathological α-synuclein (α-Syn) in Parkinson\u27s disease. Thus, molecular changes in the skin associated with ALS-specific pathological events could readily be detected and become biomarkers for ALS through skin testing. Here, we summarize the literature on pathological changes in the skin of ALS patients and animal models, including structural abnormalities of the skin, reduced density of skin nerve fibers, abnormal protein aggregation, altered mitochondrial morphology and function, and dysregulation of skin inflammation, which may be useful for early diagnosis and monitoring of ALS progression

Authors: Turner, MR; Al-Chalabi, A; Baker, I; Barritt, A; Chandran, S

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: BMJ Publishing Group
• Journal: Practical Neurology
• Volume: 22
• Issue: 3
• Pages: 176-178
• Publication date: 2022-01-06
• Acceptance date: 2021-10-26
• DOI: 10.1136/practneurol-2021-003256
• EISSN: 1474-7766
• ISSN: 1474-7758
• Language: English
• Keywords: Internal medicine; Gold coast; Medicine; Physical medicine and rehabilitation; Neuroscience; Psychology; Archaeology; Gold standard (test); Geography