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Predicting amyloid risk by machine learning algorithms based on the A4 screen data: Application to the Japanese
Kenichiro Sato1, Ryoko Ihara2,3, Kazushi Suzuki3
1Department of Neurology Graduate School of Medicine The University of Tokyo Tokyo Japan.
Machine learning models can identify elderly individuals at higher risk for amyloid buildup, aiding Alzheimer's disease prevention trials. This helps prioritize participants for efficient recruitment in preclinical Alzheimer's disease studies.
Area of Science:
- Neuroscience
- Medical Imaging
- Machine Learning
Background:
- Identifying individuals at high risk for brain amyloid deposition is crucial for Alzheimer's disease (AD) prevention trials.
- Early detection of preclinical AD is essential for effective intervention.
Purpose of the Study:
- To develop and validate machine learning models for predicting amyloid positron emission tomography (PET) standard uptake value ratio (SUVr) in cognitively normal elderly individuals.
- To assess the feasibility of using these models for participant prioritization in Alzheimer's disease prevention studies.
Main Methods:
- Machine learning models were developed using data from the Anti-Amyloid Treatment in Asymptomatic Alzheimer's Disease study.
- Models were applied to 3081 participants in the Japanese Trial-Ready Cohort (J-TRC) webstudy.
- Predictive performance was evaluated using amyloid PET SUVr and confirmed with a subgroup of 37 participants with known amyloid status.
Main Results:
- Key predictors for amyloid deposition included age, family history, and cognitive test scores (Cognitive Function Instrument, CogState).
- The machine learning models demonstrated good performance in predicting amyloid status, with an area under the curve of 0.806 in the J-TRC subgroup.
- Predicted SUVr values correlated well with self-reported amyloid test results.
Conclusions:
- The developed algorithms show potential for automatically prioritizing individuals with higher amyloid risk from the J-TRC webstudy.
- This automated prioritization can enhance the efficiency of recruiting participants for in-person studies, accelerating the identification of preclinical AD cases.
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