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Identification of Parkinson's Disease Subtypes from Resting-State Electroencephalography.
Yassine, Sahar; Gschwandtner, Ute; Auffret, Manon; Duprez, Joan; Verin, Marc; Fuhr, Peter; Hassan, Mahmoud.
Afiliação
  • Yassine S; LTSI - INSERM U1099, University of Rennes, Rennes, France.
  • Gschwandtner U; NeuroKyma, Rennes, France.
  • Auffret M; Behavior and Basal Ganglia, CIC1414, CIC-IT, CHU Rennes, Rennes, France.
  • Duprez J; Department of Neurology, Hospitals of the University of Basel, Basel, Switzerland.
  • Verin M; LTSI - INSERM U1099, University of Rennes, Rennes, France.
  • Fuhr P; Behavior and Basal Ganglia, CIC1414, CIC-IT, CHU Rennes, Rennes, France.
  • Hassan M; Institut des Neurosciences Cliniques de Rennes (INCR), Rennes, France.
Mov Disord ; 38(8): 1451-1460, 2023 08.
Article em En | MEDLINE | ID: mdl-37310340
ABSTRACT

BACKGROUND:

Parkinson's disease (PD) patients present with a heterogeneous clinical phenotype, including motor, cognitive, sleep, and affective disruptions. However, this heterogeneity is often either ignored or assessed using only clinical assessments.

OBJECTIVES:

We aimed to identify different PD sub-phenotypes in a longitudinal follow-up analysis and their electrophysiological profile based on resting-state electroencephalography (RS-EEG) and to assess their clinical significance over the course of the disease.

METHODS:

Using electrophysiological features obtained from RS-EEG recordings and data-driven methods (similarity network fusion and source-space spectral analysis), we have performed a clustering analysis to identify disease sub-phenotypes and we examined whether their different patterns of disruption are predictive of disease outcome.

RESULTS:

We showed that PD patients (n = 44) can be sub-grouped into three phenotypes with distinct electrophysiological profiles. These clusters are characterized by different levels of disruptions in the somatomotor network (Δ and ß band), the frontotemporal network (α2 band) and the default mode network (α1 band), which consistently correlate with clinical profiles and disease courses. These clusters are classified into either moderate (only-motor) or mild-to-severe (diffuse) disease. We showed that EEG features can predict cognitive evolution of PD patients from baseline, when the cognitive clinical scores were overlapped.

CONCLUSIONS:

The identification of novel PD subtypes based on electrical brain activity signatures may provide a more accurate prognosis in individual patients in clinical practice and help to stratify subgroups in clinical trials. Innovative profiling in PD can also support new therapeutic strategies that are brain-based and designed to modulate brain activity disruption. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson Idioma: En Ano de publicação: 2023 Tipo de documento: Article