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AutoML-Multiverse: An Instability-Aware Framework for Quantifying Analytic Variability in Alzheimer's Disease

Maitrei Kohli1, Gonzalo Castro Leal1, Douglas Wyllie1,2

  • 1UCL Hawkes Institute, University College London, London, UK.

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Summary
This summary is machine-generated.

Machine learning models for Alzheimer's disease (AD) can be unreliable due to analysis choices. AutoML-Multiverse addresses this by exploring thousands of analysis pipelines, improving the robustness of AD prediction models.

Keywords:
Alzheimer’s diseaseAnalytical flexibilityAutomated machine learningCross-cohort validationModel stabilityMultimodal integrationMultiverse analysisUncertainty quantification

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Area of Science:

  • Artificial Intelligence
  • Computational Neuroscience
  • Biomedical Informatics

Background:

  • Machine learning (ML) models for Alzheimer's disease (AD) often produce inconsistent results, impacting their reliability and interpretability.
  • Analytic variability and researcher biases contribute to the instability of ML models in AD research.
  • Clinical heterogeneity and cohort differences further complicate the development of robust AD prediction models.

Purpose of the Study:

  • To introduce AutoML-Multiverse, a novel framework designed to characterize how analytical choices influence ML conclusions in AD research.
  • To systematically quantify analytic instability in clinical ML models for AD.
  • To improve the robustness and clinical applicability of ML-based prediction models for Alzheimer's disease.

Main Methods:

  • Explored a vast space of approximately 20,000 analysis pipelines using the AutoML-Multiverse framework.
  • Evaluated the framework across 20 classification tasks in two independent Alzheimer's disease progression cohorts (ADNI and NACC).
  • Utilized multiple data modalities including neuroimaging, clinical/cognitive data, and fluid biomarkers.

Main Results:

  • AutoML-Multiverse demonstrated performance equal to or better than non-automated models across all classification tasks.
  • Classification accuracy for stable vs. progressive mild cognitive impairment (MCI) was 0.68±0.06 (ADNI) and 0.63±0.08 (NACC).
  • Accuracy for Alzheimer's disease (AD) vs. cognitively normal (CN) classification reached 0.97±0.01 (ADNI), with modality utility varying by task and cohort.

Conclusions:

  • Analytic choices significantly impact ML model rankings and biomarker importance in AD research.
  • Cross-cohort variability underscores the limitations of single-dataset studies and highlights the need for instability-aware evaluation.
  • The AutoML-Multiverse framework enhances the robustness of AI-driven research by reducing analysis-driven variability and characterizing uncertainty.