PET-validated EEG-machine learning algorithm predicts brain amyloid pathology in pre-dementia Alzheimer's disease

초록

Developing reliable biomarkers is important for screening Alzheimer's disease (AD) and monitoring its progression. Although EEG is non-invasive direct measurement of brain neural activity and has potentials for various neurologic disorders, vulnerability to noise, difficulty in clinical interpretation and quantification of signal information have limited its clinical application. There have been many research about machine learning (ML) adoption with EEG, but the accuracy of detecting AD is not so high or not validated with A beta PET scan. We developed EEG-ML algorithm to detect brain A beta pathology among subjective cognitive decline (SCD) or mild cognitive impairment (MCI) population, and validated it with A beta PET. 19-channel resting-state EEG and A beta PET were collected from 311 subjects: 196 SCD(36 A beta+, 160 A beta -), 115 MCI(54 A beta+, 61A beta -). 235 EEG data were used for training ML, and 76 for validation. EEG features were standardized for age and sex. Multiple important features sets were selected by 6 statistics analysis. Then, we trained 8 multiple machine learning for each important features set. Meanwhile, we conducted paired t-test to find statistically different features between amyloid positive and negative group. The best model showed 90.9% sensitivity, 76.7% specificity and 82.9% accuracy in MCI+SCD (33 A beta+, 43 A beta -). Limited to SCD, 92.3% sensitivity, 75.0% specificity, 81.1% accuracy (13 A beta+, 24 A beta -). 90% sensitivity, 78.9% specificity and 84.6% accuracy for MCI (20 A beta+, 19 A beta -). Similar trends of EEG power have been observed from the group comparison between A beta+and A beta -, and between MCI and SCD: enhancement of frontal/ frontotemporal theta; attenuation of mid-beta in centroparietal areas. The present findings suggest that accurate classification for beta-amyloid accumulation in the brain based on QEEG alone could be possible, which implies that QEEG is a promising biomarker for beta-amyloid. Since QEEG is more accessible, cost-effective, and safer than amyloid PET, QEEG-based biomarkers may play an important role in the diagnosis and treatment of AD. We expect specific patterns in QEEG could play an important role to predict future progression of cognitive impairment in the preclinical stage of AD. Further feature engineering and validation with larger dataset is recommended.

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