Validation of machine learning models to detect amyloid pathologies across institutions

被引:0
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作者
Juan C. Vizcarra
Marla Gearing
Michael J. Keiser
Jonathan D. Glass
Brittany N. Dugger
David A. Gutman
机构
[1] Georgia Institute of Technology and Emory University,The Wallace H. Coulter Department of Biomedical Engineering
[2] Emory University School of Medicine,Department of Neurology
[3] Emory University School of Medicine,Department of Pathology and Laboratory Medicine
[4] Institute for Neurodegenerative Diseases,Department of Pharmaceutical Chemistry, Department of Bioengineering and Therapeutic Sciences
[5] Kavli Institute for Fundamental Neuroscience,Center for Neurodegenerative Disease
[6] and Bakar Computational Health Sciences Institute,Department of Pathology and Laboratory Medicine
[7] University of California,undefined
[8] Emory University School of Medicine,undefined
[9] Whitehead Biomedical Research Building,undefined
[10] University of California-Davis School of Medicine,undefined
关键词
Neuropathology; Deep learning; Amyloid beta; Alzheimer’s disease; Concomitant diagnosis; Whole-slide imaging;
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摘要
Semi-quantitative scoring schemes like the Consortium to Establish a Registry for Alzheimer’s Disease (CERAD) are the most commonly used method in Alzheimer’s disease (AD) neuropathology practice. Computational approaches based on machine learning have recently generated quantitative scores for whole slide images (WSIs) that are highly correlated with human derived semi-quantitative scores, such as those of CERAD, for Alzheimer’s disease pathology. However, the robustness of such models have yet to be tested in different cohorts. To validate previously published machine learning algorithms using convolutional neural networks (CNNs) and determine if pathological heterogeneity may alter algorithm derived measures, 40 cases from the Goizueta Emory Alzheimer’s Disease Center brain bank displaying an array of pathological diagnoses (including AD with and without Lewy body disease (LBD), and / or TDP-43-positive inclusions) and levels of Aβ pathologies were evaluated. Furthermore, to provide deeper phenotyping, amyloid burden in gray matter vs whole tissue were compared, and quantitative CNN scores for both correlated significantly to CERAD-like scores. Quantitative scores also show clear stratification based on AD pathologies with or without additional diagnoses (including LBD and TDP-43 inclusions) vs cases with no significant neurodegeneration (control cases) as well as NIA Reagan scoring criteria. Specifically, the concomitant diagnosis group of AD + TDP-43 showed significantly greater CNN-score for cored plaques than the AD group. Finally, we report that whole tissue computational scores correlate better with CERAD-like categories than focusing on computational scores from a field of view with densest pathology, which is the standard of practice in neuropathological assessment per CERAD guidelines. Together these findings validate and expand CNN models to be robust to cohort variations and provide additional proof-of-concept for future studies to incorporate machine learning algorithms into neuropathological practice.
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