Machine Learning for the Prediction of Amyloid Positivity in Amnestic Mild Cognitive Impairment

Author:

Kang Sung Hoon123,Cheon Bo Kyoung124,Kim Ji-Sun12,Jang Hyemin12,Kim Hee Jin12,Park Kyung Won5,Noh Young6,Lee Jin San7,Ye Byoung Seok8,Na Duk L.12,Lee Hyejoo12,Seo Sang Won124910

Affiliation:

1. Departments of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

2. Neuroscience Center, Samsung Medical Center, Seoul, Korea

3. Department of Neurology, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Korea

4. Department of Digital Health, SAIHST, Sungkyunkwan University, Seoul, Korea

5. Department of Neurology, Dong-A University Medical Center, Dong-A University College of Medicine, Busan, Korea

6. Department of Neurology, Gachon University Gil Medical Center, Incheon, Korea

7. Department of Neurology, Kyung Hee University Hospital, Seoul, Korea

8. Department of Neurology, Severance hospital, Yonsei University School of Medicine, Seoul, Korea

9. Samsung Alzheimer Research Center and Center for Clinical Epidemiology Medical Center, Seoul, Korea

10. Department of Intelligent Precision Healthcare Convergence, SAIHST, Sungkyunkwan University, Seoul, Korea

Abstract

Background: Amyloid-β (Aβ) evaluation in amnestic mild cognitive impairment (aMCI) patients is important for predicting conversion to Alzheimer’s disease. However, Aβ evaluation through Aβ positron emission tomography (PET) is limited due to high cost and safety issues. Objective: We therefore aimed to develop and validate prediction models of Aβ positivity for aMCI using optimal interpretable machine learning (ML) approaches utilizing multimodal markers. Methods: We recruited 529 aMCI patients from multiple centers who underwent Aβ PET. We trained ML algorithms using a training cohort (324 aMCI from Samsung medical center) with two-phase modelling: model 1 included age, gender, education, diabetes, hypertension, apolipoprotein E genotype, and neuropsychological test scores; model 2 included the same variables as model 1 with additional MRI features. We used four-fold cross-validation during the modelling and evaluated the models on an external validation cohort (187 aMCI from the other centers). Results: Model 1 showed good accuracy (area under the receiver operating characteristic curve [AUROC] 0.837) in cross-validation, and fair accuracy (AUROC 0.765) in external validation. Model 2 led to improvement in the prediction performance with good accuracy (AUROC 0.892) in cross validation compared to model 1. Apolipoprotein E genotype, delayed recall task scores, and interaction between cortical thickness in the temporal region and hippocampal volume were the most important predictors of Aβ positivity. Conclusion: Our results suggest that ML models are effective in predicting Aβ positivity at the individual level and could help the biomarker-guided diagnosis of prodromal AD.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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