Alzheimer’s disease (AD) is a progressive neurodegenerative disorder that significantly affects cognitive function. Early and accurate diagnosis is crucial for timely intervention, yet traditional diagnostic methods can be costly and invasive. This study explores a machine learning (ML) approach leveraging the Bio-Hermes dataset, which integrates blood-derived proteomics, neuropsychological test results, and demographic variables to improve the classification of individuals into cognitively normal (CN), mild cognitive impairment (MCI), and AD categories. We implement four ML models: Elastic Net, Classification and Regression Trees (CART), Random Forest, and Extreme Gradient Boosting (XGBoost). The results indicate that XGBoost achieves the highest accuracy (0.81) and a strong area under the receiver operating characteristic curve (AUCROC) (0.94), highlighting the potential of multimodal ML models in dementia classification. Additionally, the Mini-Mental State Exam (MMSE) and the proteomic marker pTau181 emerged as key predictive variables. This study underscores the feasibility of using blood-based proteomics in conjunction with cognitive assessments for early AD detection and advocates for further validation on larger, diverse cohorts.

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Proteomics, Neuropsychological and Demographics Multimodal Machine Learning Approach to Alzheimer’s Disease Prediction on the Bio-Hermes Study Cohort

  • Henry Musto,
  • Daniel Stamate,
  • David Reeves,
  • Catharine Morgan,
  • Roxana Hutanu,
  • Kalliopi Mavromati,
  • Dorina Cadar,
  • Daniel Stahl

摘要

Alzheimer’s disease (AD) is a progressive neurodegenerative disorder that significantly affects cognitive function. Early and accurate diagnosis is crucial for timely intervention, yet traditional diagnostic methods can be costly and invasive. This study explores a machine learning (ML) approach leveraging the Bio-Hermes dataset, which integrates blood-derived proteomics, neuropsychological test results, and demographic variables to improve the classification of individuals into cognitively normal (CN), mild cognitive impairment (MCI), and AD categories. We implement four ML models: Elastic Net, Classification and Regression Trees (CART), Random Forest, and Extreme Gradient Boosting (XGBoost). The results indicate that XGBoost achieves the highest accuracy (0.81) and a strong area under the receiver operating characteristic curve (AUCROC) (0.94), highlighting the potential of multimodal ML models in dementia classification. Additionally, the Mini-Mental State Exam (MMSE) and the proteomic marker pTau181 emerged as key predictive variables. This study underscores the feasibility of using blood-based proteomics in conjunction with cognitive assessments for early AD detection and advocates for further validation on larger, diverse cohorts.