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Alzheimer's Disease (AD) is a continually advancing neurodegenerative disorder, distinguished by escalating memory loss, cognitive dysfunction, and dementia. The disease unfolds in three stages: preclinical, mild cognitive impairment (MCI), and dementia. Its onset is insidious, and the progression gradual, with the cause not well explained by other disorders.
The clinical diagnosis of AD hinges on the presence of memory and other cognitive impairments. Biomarkers, such as changes in Aβ...
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A Machine Learning Approach to Design an Efficient Selective Screening of Mild Cognitive Impairment
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Predicting Amyloid-β Levels in Amnestic Mild Cognitive Impairment Using Machine Learning Techniques.

Ali Ezzati1,2, Danielle J Harvey3, Christian Habeck4

  • 1Department of Neurology, Albert Einstein College of Medicine, Bronx, NY, USA.

Journal of Alzheimer'S Disease : JAD
|December 30, 2019
PubMed
Summary

Machine learning models can predict amyloid-beta (Aβ) positivity in individuals with mild cognitive impairment. Cerebrospinal fluid biomarkers significantly improve prediction accuracy for Alzheimer's disease clinical trial eligibility.

Keywords:
Alzheimer’s diseaseamyloid imagingmachine learningmild cognitive impairmentpredictive analytics

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Area of Science:

  • Neuroimaging and Biomarkers
  • Machine Learning in Medicine
  • Alzheimer's Disease Research

Background:

  • Amyloid-beta (Aβ) positivity via PET imaging is crucial for Alzheimer's disease (AD) clinical trial enrollment, especially for amyloid-targeted therapies.
  • Predicting Aβ status pre-PET can reduce patient burden and trial costs.

Purpose of the Study:

  • To evaluate a machine learning model's performance in predicting individual Aβ positivity risk.
  • Utilizing PET imaging as the gold standard for Aβ status confirmation.

Main Methods:

  • Data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) amnestic mild cognitive impairment (aMCI) cohort were used.
  • Models incorporated demographics, ApoE4 status, neuropsychological tests (NP), MRI volumetrics, and cerebrospinal fluid (CSF) biomarkers.

Main Results:

  • Models with NP and MRI measures achieved AUCs of 0.74 and 0.72, respectively.
  • Combining NP and MRI did not enhance prediction.
  • Models incorporating CSF biomarkers demonstrated superior performance with AUCs ranging from 0.89 to 0.92.

Conclusions:

  • Predictive models are effective in identifying individuals with aMCI who are likely to be amyloid-positive.
  • This approach aids in streamlining patient selection for AD clinical trials.