Monitoring Alzheimer's Disease Progression in Mild Cognitive Impairment Stage Using Machine Learning-Based FDG-PET Classification Methods

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Abstract

Background: We previously introduced a machine learning-based Alzheimer's Disease Designation (MAD) framework for identifying AD-related metabolic patterns among neurodegenerative subjects. Objective: We sought to assess the efficiency of our MAD framework for tracing the longitudinal brain metabolic changes in the prodromal stage of AD. Methods: MAD produces subject scores using five different machine-learning algorithms, which include a general linear model (GLM), two different approaches of scaled subprofile modeling, and two different approaches of a support vector machine. We used our pre-trained MAD framework, which was trained based on metabolic brain features of 94 patients with AD and 111 age-matched cognitively healthy (CH) individuals. The MAD framework was applied on longitudinal independent test sets including 54 CHs, 51 stable mild cognitive impairment (sMCI), and 39 prodromal AD (pAD) patients at the time of the clinical diagnosis of AD, and two years prior. Results: The GLM showed excellent performance with area under curve (AUC) of 0.96 in distinguishing sMCI from pAD patients at two years prior to the time of the clinical diagnosis of AD while other methods showed moderate performance (AUC: 0.7-0.8). Significant annual increment of MAD scores were identified using all five algorithms in pAD especially when it got closer to the time of diagnosis (p < 0.001), but not in sMCI. The increased MAD scores were also significantly associated with cognitive decline measured by Mini-Mental State Examination in pAD (q < 0.01). Conclusion: These results suggest that MAD may be a relevant tool for monitoring disease progression in the prodromal stage of AD.
Original languageEnglish
Pages (from-to)1493-1502
Number of pages10
JournalJournal of Alzheimer's Disease
Volume89
Issue number4
DOIs
StatePublished - Sep 2 2022

Bibliographical note

Publisher Copyright:
© 2022 - The authors. Published by IOS Press.

Funding

This study is supported by grant number RGPIN-2016-05964 from Natural Science and Engineering Research Council of Canada (NSERC). Student stipends and postdoctoral salary support was provided by MITACS and Parkinson Canada. For MAD algorithm development, data collection and sharing were funded by the Alzheimer’s Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant U01 AG024904) and DOD ADNI (Department of Defense award number W81XWH-12-2-0012). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: AbbVie, Alzheimer’s Association; Alzheimer’s Drug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen; Bristol-Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hoffmann-La Roche Ltd and its affiliated company Genentech, Inc.; Fujirebio; GE Healthcare; IXICO Ltd.;Janssen Alzheimer Immunotherapy Research & Development, LLC.; Johnson & Johnson Pharmaceutical Research & Development LLC.; Lumosity; Lundbeck; Merck & Co., Inc.;Meso Scale Diagnostics, LLC.; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health (https://www.fnih.org). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer’s Therapeutic Research Institute at the University of Southern California. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California. We also acknowledge support from the St. Boniface Hospital Research Foundation (Grant Nos. 1406–3216 and 1410–3216), the Canadian Institute of Health Research (CIHR; Grant No. PJT-162144) to B.C.A., the Honourable Douglas and Patricia Everett, Royal Canadian Properties Limited Endowment Fund (Grant No. 1403–3131) to B.C.A. B.C.A. also previously held the Manitoba Dementia Research Chair (funded by the Alzheimer’s Society of Manitoba and Research Manitoba).

FundersFunder number
Natural Sciences and Engineering Research Council of CanadaRGPIN-2016-05964
Alzheimer’s Disease Neuroimaging InitiativeNational Institutes of Health Grant U01 AG024904
Alzheimer’s Disease Neuroimaging InitiativeDepartment of Defense award number W81XWH-12-2-0012
St. Boniface Hospital Research Foundation1406–3216, 1410–3216
Canadian Institutes of Health ResearchPJT-162144

    ASJC Scopus Subject Areas

    • General Neuroscience
    • Clinical Psychology
    • Geriatrics and Gerontology
    • Psychiatry and Mental health

    Keywords

    • Alzheimer's disease
    • brain metabolism
    • FDG PET
    • machine learning
    • Humans
    • Fluorodeoxyglucose F18
    • Alzheimer Disease/diagnostic imaging
    • Cognitive Dysfunction/diagnostic imaging
    • Prodromal Symptoms
    • Machine Learning
    • Disease Progression

    Disciplines

    • Pharmacy and Pharmaceutical Sciences

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