Practical Geriatrics ›› 2025, Vol. 39 ›› Issue (2): 116-120.doi: 10.3969/j.issn.1003-9198.2025.02.003

Previous Articles     Next Articles

Advances in the diagnosis of multiple system atrophy

LI Lin, LIU Anru, WAN Lijun, LIU Xuewu   

  1. Department of Neurology, Qilu Hospital of Shandong University, Jinan 250012, China(LI Lin);Department of Neurology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, China(LIU Anru); Department of Neurology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan 250021, China(WAN Lijun, LIU Xuewu)
  • Received:2024-10-25 Online:2025-02-20 Published:2025-03-03
  • Contact: LIU Xuewu, Email: snlxw1966@163.com

Abstract: Multiple system atrophy(MSA) is a rapidly progressive neurodegenerative disease characterized by a variety of clinical symptoms such as Parkinson's disease-like symptom clusters, cerebellar ataxia and autonomic dysfunction. At present, the biomarkers used in clinical diagnosis of MSA lack specificity, which makes early diagnosis difficult and easy to misdiagnose. MRI and cerebro spinal fluid(CSF) examination can assist in the diagnosis of MSA, but they are costly and have low specificity. It will take some time for the latest early detection technology of MSA, α-synuclein positron emission computed tomography (PET) imaging, to be applied in clinical practice. Blood and urine α-synuclein testing has the potential to be used in clinical diagnosis. Neurofilament light chain (NfL) and glial fibrillary acidic protein(GFAP) can also be used as biomarkers for the diagnosis of MSA, but further research is needed. The development of precise molecular biomarkers for the diagnosis of MSA is crucial, as it can revolutionize the diagnosis and treatment of MSA, and will facilitate early intervention and improve prognosis of the disease.

Key words: multiple system atrophy, diagnosis, parkinson's disease, α-synuclein

CLC Number: