» Articles » PMID: 38600857

Automatic Sleep-wake Classification and Parkinson's Disease Recognition Using Multifeature Fusion with Support Vector Machine

Overview
Specialties Neurology
Pharmacology
Date 2024 Apr 11
PMID 38600857
Authors
Affiliations
Soon will be listed here.
Abstract

Aims: Sleep disturbance is a prevalent nonmotor symptom of Parkinson's disease (PD), however, assessing sleep conditions is always time-consuming and labor-intensive. In this study, we performed an automatic sleep-wake state classification and early diagnosis of PD by analyzing the electrocorticography (ECoG) and electromyogram (EMG) signals of both normal and PD rats.

Methods: The study utilized ECoG power, EMG amplitude, and corticomuscular coherence values extracted from normal and PD rats to construct sleep-wake scoring models based on the support vector machine algorithm. Subsequently, we incorporated feature values that could act as diagnostic markers for PD and then retrained the models, which could encompass the identification of vigilance states and the diagnosis of PD.

Results: Features extracted from occipital ECoG signals were more suitable for constructing sleep-wake scoring models than those from frontal ECoG (average Cohen's kappa: 0.73 vs. 0.71). Additionally, after retraining, the new models demonstrated increased sensitivity to PD and accurately determined the sleep-wake states of rats (average Cohen's kappa: 0.79).

Conclusion: This study accomplished the precise detection of substantia nigra lesions and the monitoring of sleep-wake states. The integration of circadian rhythm monitoring and disease state assessment has the potential to improve the efficacy of therapeutic strategies considerably.

Citing Articles

Automatic sleep-wake classification and Parkinson's disease recognition using multifeature fusion with support vector machine.

Shen Y, Huai B, Wang X, Chen M, Shen X, Han M CNS Neurosci Ther. 2024; 30(4):e14708.

PMID: 38600857 PMC: 11007385. DOI: 10.1111/cns.14708.

References
1.
French I, Muthusamy K . A Review of Sleep and Its Disorders in Patients with Parkinson's Disease in Relation to Various Brain Structures. Front Aging Neurosci. 2016; 8:114. PMC: 4876118. DOI: 10.3389/fnagi.2016.00114. View

2.
Liu J, Sheng Y, Liu H . Corticomuscular Coherence and Its Applications: A Review. Front Hum Neurosci. 2019; 13:100. PMC: 6435838. DOI: 10.3389/fnhum.2019.00100. View

3.
Li Y, Luo Y, Xu W, Ge J, Cherasse Y, Wang Y . Ventral pallidal GABAergic neurons control wakefulness associated with motivation through the ventral tegmental pathway. Mol Psychiatry. 2020; 26(7):2912-2928. PMC: 8505244. DOI: 10.1038/s41380-020-00906-0. View

4.
Dejean C, Arbuthnott G, Wickens J, Le Moine C, Boraud T, Hyland B . Power fluctuations in beta and gamma frequencies in rat globus pallidus: association with specific phases of slow oscillations and differential modulation by dopamine D1 and D2 receptors. J Neurosci. 2011; 31(16):6098-107. PMC: 6632973. DOI: 10.1523/JNEUROSCI.3311-09.2011. View

5.
Sharott A, Magill P, Harnack D, Kupsch A, Meissner W, Brown P . Dopamine depletion increases the power and coherence of beta-oscillations in the cerebral cortex and subthalamic nucleus of the awake rat. Eur J Neurosci. 2005; 21(5):1413-22. DOI: 10.1111/j.1460-9568.2005.03973.x. View