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Altered Low-beta Characteristics in Individuals With Alcohol Use Disorder: A Pilot Resting Electroencephalography
Bing Li1,2, Jie Wang1,2, Shuaiyu Long1,2
1Hebei Provincial Mental Health Center, 071000 Baoding, Hebei, China.
Resting-state electroencephalography (EEG) with power spectral analysis (PSA) and dynamic functional connectivity (dFC) may offer objective biomarkers for alcohol use disorder (AUD). This study found distinct EEG patterns in AUD patients, suggesting potential for improved diagnosis.
Area of Science:
- Neuroscience
- Clinical Psychology
- Biomarker Discovery
Background:
- Alcohol use disorder (AUD) pathophysiology is poorly understood, and current clinical assessments rely on subjective measures.
- Objective biomarkers for AUD diagnosis are lacking, hindering effective clinical evaluation and treatment.
Purpose of the Study:
- To explore resting-state electroencephalography (EEG) with power spectral analysis (PSA) and dynamic functional connectivity (dFC) as potential objective biomarkers for AUD.
- To differentiate individuals with AUD from healthy controls (HCs) using neurophysiological measures.
Main Methods:
- A case-control study involving resting-state EEG data collection from individuals with AUD and HCs.
- Power spectral analysis (PSA) to quantify EEG energy distribution and receiver operating characteristic (ROC) analysis for discriminatory capacity.
- Dynamic functional connectivity (dFC) analysis using a sliding window approach and weighted phase-lag index (wPLI) to identify brain states.
Main Results:
- The AUD group showed significantly elevated low-beta power at specific frontal and central electrode sites compared to HCs, with high diagnostic accuracy (AUC > 0.76).
- dFC analysis identified three distinct brain connectivity states (S1, S2, S3) with varying proportions.
- Correlations were found between identified connectivity patterns and clinical indices within the AUD cohort.
Conclusions:
- Resting-state EEG, particularly when analyzed with PSA and dFC, shows promise as a potential objective biomarker for AUD detection.
- Increased brain activity in medial frontal and left central gyri, along with low-beta frequency changes in dFC, are characteristic of AUD.
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