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Multiple system atrophy: advances in pathophysiology, diagnosis, and treatment. | LitMetric

AI Article Synopsis

  • Multiple system atrophy (MSA) is a rare, progressive neurological disorder that usually starts in adulthood and features a variety of both motor and non-motor symptoms, often resembling other conditions like Parkinson's disease.
  • Research over the past five years has deepened understanding of MSA, particularly regarding the role of α-synuclein inclusions, which are linked to the disease's progression.
  • Updated diagnostic criteria in 2022 aim to improve early diagnosis, and while recent clinical trials show promise for new treatments, definitive evidence of neuroprotection is still lacking.

Article Abstract

Multiple system atrophy is an adult-onset, sporadic, and progressive neurodegenerative disease. People with this disorder report a wide range of motor and non-motor symptoms. Overlap in the clinical presentation of multiple system atrophy with other movement disorders (eg, Parkinson's disease and progressive supranuclear palsy) is a concern for accurate and timely diagnosis. Over the past 5 years, progress has been made in understanding key pathophysiological events in multiple system atrophy, including the seeding of α-synuclein inclusions and the detection of disease-specific α-synuclein strains. Diagnostic criteria were revised in 2022 with the intention to improve the accuracy of a diagnosis of multiple system atrophy, particularly for early disease stages. Early signals of efficacy in clinical trials have indicated the potential for disease-modifying therapies for multiple system atrophy, although no trial has yet provided unequivocal evidence of neuroprotection in this rare disease. The advances in pathophysiology could play a part in biomarker discovery for early diagnosis as well as in the development of disease-modifying therapies.

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Source
http://dx.doi.org/10.1016/S1474-4422(24)00396-XDOI Listing

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