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Predicting Alzheimer's disease CSF core biomarkers: a multimodal Machine Learning approach
Anna Michela Gaeta1, María Quijada-López2, Ferran Barbé3,4
1Servicio de Neumología, Hospital Universitario Severo Ochoa, Leganés, Spain.
Frontiers in Aging Neuroscience
|July 11, 2024
Summary
Machine learning models can predict Alzheimer's disease (AD) biomarkers using non-invasive sleep data. This approach offers a promising, cost-effective screening tool for early AD detection and risk assessment.
Area of Science:
- Neuroscience
- Biomarker Discovery
- Machine Learning
Background:
- Alzheimer's disease (AD) diagnosis relies on invasive cerebrospinal fluid (CSF) biomarkers, limiting their use in screening.
- Sleep disturbances are linked to AD pathology, suggesting potential for non-invasive biomarkers.
- Quantitative analysis of polysomnography (PSG) signals for AD detection is underexplored.
Purpose of the Study:
- To evaluate a multimodal machine learning (ML) approach for predicting core AD CSF biomarkers.
- To assess the effectiveness of non-invasive quantitative sleep electroencephalography (EEG) features as AD biomarkers.
- To determine if ML can identify AD neuropathology using accessible data.
Main Methods:
- Recruited mild-moderate AD patients for PSG, CSF, and blood biomarker analysis.
- Extracted quantitative features (non-linear, time, frequency domains) from PSG signals.
- Trained ML algorithms on clinical variables (CLINVAR), conventional PSG (SLEEPVAR), quantitative PSG (PSGVAR), and combined (ALL) features.
Main Results:
- Gradient Boosting Regressors showed best performance in estimating biomarker levels.
- The combined feature subset (ALL) generally yielded the lowest training errors.
- The SLEEPVAR subset excelled in predicting Aβ42, while ALL best predicted p-tau and t-tau.
Conclusions:
- Multimodal ML effectively predicts CSF biomarkers in early AD using non-invasive data.
- This approach provides a feasible and economical screening tool for AD risk.
- Integrating computational models aids clinical decisions and early AD patient identification.

