Frontiers in Aging Neuroscience (Feb 2024)

Comparative analysis of multimodal biomarkers for amyloid-beta positivity detection in Alzheimer's disease cohorts

  • Mostafa Mehdipour Ghazi,
  • Per Selnes,
  • Per Selnes,
  • Santiago Timón-Reina,
  • Sandra Tecelão,
  • Silvia Ingala,
  • Atle Bjørnerud,
  • Atle Bjørnerud,
  • Bjørn-Eivind Kirsebom,
  • Bjørn-Eivind Kirsebom,
  • Tormod Fladby,
  • Tormod Fladby,
  • Mads Nielsen

DOI
https://doi.org/10.3389/fnagi.2024.1345417
Journal volume & issue
Vol. 16

Abstract

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IntroductionEfforts to develop cost-effective approaches for detecting amyloid pathology in Alzheimer's disease (AD) have gained significant momentum with a focus on biomarker classification. Recent research has explored non-invasive and readily accessible biomarkers, including magnetic resonance imaging (MRI) biomarkers and some AD risk factors.MethodsIn this comprehensive study, we leveraged a diverse dataset, encompassing participants with varying cognitive statuses from multiple sources, including cohorts from the Alzheimer's Disease Neuroimaging Initiative (ADNI) and our in-house Dementia Disease Initiation (DDI) cohort. As brain amyloid plaques have been proposed as sufficient for AD diagnosis, our primary aim was to assess the effectiveness of multimodal biomarkers in identifying amyloid plaques, using deep machine learning methodologies.ResultsOur findings underscore the robustness of the utilized methods in detecting amyloid beta positivity across multiple cohorts. Additionally, we investigated the potential of demographic data to enhance MRI-based amyloid detection. Notably, the inclusion of demographic risk factors significantly improved our models' ability to detect amyloid-beta positivity, particularly in early-stage cases, exemplified by an average area under the ROC curve of 0.836 in the unimpaired DDI cohort.DiscussionThese promising, non-invasive, and cost-effective predictors of MRI biomarkers and demographic variables hold the potential for further refinement through considerations like APOE genotype and plasma markers.

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