Individualized Spectral Features in First-Episode and Drug-Naïve Major Depressive Disorder: Insights From Periodic and Aperiodic Electroencephalography Analysis.

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Tác giả: Chenyang Gao, Yuanyuan Huang, Jiaxin Li, Zhaobo Li, Yuping Ning, Fengchun Wu, Kai Wu, Dongsheng Xiong, Jing Zhou

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: United States : Biological psychiatry. Cognitive neuroscience and neuroimaging , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 700977

BACKGROUND: The detection of abnormal brain activity plays an important role in the early diagnosis and treatment of major depressive disorder (MDD). Recent studies have shown that the decomposition of the electroencephalography (EEG) spectrum into periodic and aperiodic components is useful for identifying the drivers of electrophysiologic abnormalities and avoiding individual differences. METHODS: In this study, we aimed to elucidate the pathological changes in individualized periodic and aperiodic activities and their relationships with the symptoms of MDD. EEG data in the eyes-closed resting state were continuously recorded from 97 first-episode and drug-naïve patients with MDD and 90 healthy control participants. Both periodic oscillations and aperiodic components were obtained via the fitting oscillations and one-over f (FOOOF) algorithm and then used to compute individualized spectral features. RESULTS: Patients with MDD presented higher canonical alpha and beta band power but lower aperiodic-adjusted alpha and beta power. Furthermore, we found that alpha power was strongly correlated with the age of patients but not with disease symptoms. The aperiodic intercept was lower in the parieto-occipital region and was positively correlated with Hamilton Depression Rating Scale scores after accounting for age and sex. In the asymmetry analysis, alpha activity appeared asymmetrical only in the healthy control group, whereas aperiodic activity was symmetrical in both groups. CONCLUSIONS: The findings of this study provide insights into the role of abnormal neural spiking activity and impaired neuroplasticity in MDD progression and suggest that the aperiodic intercept in resting-state EEG may be a potential biomarker of MDD.
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