Affiliation:
1. Institute of Clinical Neuroscience and Medical Psychology, Medical Faculty Heinrich Heine University Düsseldorf Germany
2. Center of Movement Disorders and Neuromodulation, Department of Neurology University Hospital Düsseldorf Düsseldorf Germany
Abstract
AbstractBackgroundDiagnosis of atypical parkinsonian syndromes (APS) mostly relies on clinical presentation as well as structural and molecular brain imaging. Whether parkinsonian syndromes are distinguishable based on neuronal oscillations has not been investigated so far.ObjectiveThe aim was to identify spectral properties specific to atypical parkinsonism.MethodsWe measured resting‐state magnetoencephalography in 14 patients with corticobasal syndrome (CBS), 16 patients with progressive supranuclear palsy (PSP), 33 patients with idiopathic Parkinson's disease, and 24 healthy controls. We compared spectral power as well as amplitude and frequency of power peaks between groups.ResultsAtypical parkinsonism was associated with spectral slowing, distinguishing both CBS and PSP from Parkinson's disease (PD) and age‐matched healthy controls. Patients with atypical parkinsonism showed a shift in β peaks (13–30 Hz) toward lower frequencies in frontal areas bilaterally. A concomitant increase in θ/α power relative to controls was observed in both APS and PD.ConclusionSpectral slowing occurs in atypical parkinsonism, affecting frontal β oscillations in particular. Spectral slowing with a different topography has previously been observed in other neurodegenerative disorders, such as Alzheimer's disease, suggesting that spectral slowing might be an electrophysiological marker of neurodegeneration. As such, it might support differential diagnosis of parkinsonian syndromes in the future. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
Subject
Neurology (clinical),Neurology
Cited by
3 articles.
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