Psychiatry Investig.  2023 Dec;20(12):1195-1203. 10.30773/pi.2023.0052.

A Case-Control Clinical Trial on a Deep Learning-Based Classification System for Diagnosis of Amyloid-Positive Alzheimer’s Disease

Affiliations
  • 1Department of Neuropsychiatry, Seoul National University Bundang Hospital, Seongnam, Republic of Korea
  • 2Department of Psychiatry, Seoul National University, College of Medicine, Seoul, Republic of Korea
  • 3Department of Brain and Cognitive Sciences, Seoul National University College of Natural Sciences, Seoul, Republic of Korea
  • 4VUNO Inc., Seoul, Republic of Korea
  • 5Institute of Human Behavioral Medicine, Seoul National University Medical Research Center, Seoul, Republic of Korea
  • 6Department of Radiology, Seoul National University Bundang Hospital, Seongnam, Republic of Korea
  • 7Department of Nuclear Medicine, Seoul National University Bundang Hospital, Seongnam, Republic of Korea
  • 8Center for Nanomolecular Imaging and Innovative Drug Development, Advanced Institutes of Convergence Technology, Suwon, Republic of Korea

Abstract


Objective
A deep learning-based classification system (DLCS) which uses structural brain magnetic resonance imaging (MRI) to diagnose Alzheimer’s disease (AD) was developed in a previous recent study. Here, we evaluate its performance by conducting a single-center, case-control clinical trial.
Methods
We retrospectively collected T1-weighted brain MRI scans of subjects who had an accompanying measure of amyloid-beta (Aβ) positivity based on a 18F-florbetaben positron emission tomography scan. The dataset included 188 Aβ-positive patients with mild cognitive impairment or dementia due to AD, and 162 Aβ-negative controls with normal cognition. We calculated the sensitivity, specificity, positive predictive value, negative predictive value, and area under the receiver operating characteristic curve (AUC) of the DLCS in the classification of Aβ-positive AD patients from Aβ-negative controls.
Results
The DLCS showed excellent performance, with sensitivity, specificity, positive predictive value, negative predictive value, and AUC of 85.6% (95% confidence interval [CI], 79.8–90.0), 90.1% (95% CI, 84.5–94.2), 91.0% (95% CI, 86.3–94.1), 84.4% (95% CI, 79.2–88.5), and 0.937 (95% CI, 0.911–0.963), respectively.
Conclusion
The DLCS shows promise in clinical settings where it could be routinely applied to MRI scans regardless of original scan purpose to improve the early detection of AD.

Keyword

Alzheimer disease; Magnetic resonance imaging; Clinical trial; Deep learning
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