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Updated: Aug 2, 2026

Visualization of Amyloid β Deposits in the Human Brain with Matrix-assisted Laser Desorption/Ionization Imaging Mass Spectrometry
Published on: March 7, 2019
MRAβ: A multimodal MRI-derived amyloid-β biomarker for Alzheimer's disease
1Department of Radiology and Tianjin Key Lab of Functional Imaging, Tianjin Medical University General Hospital, Tianjin, China.
Abstract:
Florbetapir 18 F (AV45), a highly sensitive and specific positron emission tomographic (PET) molecular biomarker binding to the amyloid-β of Alzheimer's disease (AD), is constrained by radiation and cost. We sought to combat it by combining multimodal magnetic resonance imaging (MRI) images and a collaborative generative adversarial networks model (CollaGAN) to develop a multimodal MRI-derived Amyloid-β (MRAβ) biomarker. We collected multimodal MRI and PET AV45 data of 380 qualified participants from the ADNI dataset and 64 subjects from OASIS3 dataset. A five-fold cross-validation CollaGAN were applied to generate MRAβ. In the ADNI dataset, we found MRAβ could characterize the subject-level AV45 spatial variations in both AD and mild cognitive impairment (MCI). Voxel-wise two-sample t-tests demonstrated amyloid-β depositions identified by MRAβ in AD and MCI were significantly higher than healthy controls (HCs) in widespread cortices (p < .05, corrected) and were much similar to those by AV45 (r > .92, p < .001). Moreover, a 3D ResNet classifier demonstrated that MRAβ was comparable to AV45 in discriminating AD from HC in both the ADNI and OASIS3 datasets, and in discriminate MCI from HC in ADNI. Finally, we found MRAβ could mimic cortical hyper-AV45 in HCs who later converted to MCI (r = .79, p < .001) and was comparable to AV45 in discriminating them from stable HC (p > .05). In summary, our work illustrates that MRAβ synthesized by multimodal MRI could mimic the cerebral amyloid-β depositions like AV45 and lends credence to the feasibility of advancing MRI toward molecular-explainable biomarkers.
Insights
A new multimodal MRI-derived biomarker (MRAβ) effectively mimics Alzheimer's disease amyloid-β PET imaging (AV45), offering a radiation-free, cost-effective alternative for diagnosis and prediction.
Area of Science:
- Neuroimaging
- Biomarker Development
- Artificial Intelligence in Medicine
Background:
- Florbetapir 18 F (AV45) PET imaging is a sensitive biomarker for Alzheimer's disease (AD) amyloid-β but is limited by radiation exposure and cost.
- Developing non-irradiating, cost-effective biomarkers is crucial for widespread AD diagnosis and monitoring.
Purpose of the Study:
- To develop a multimodal MRI-derived Amyloid-β (MRAβ) biomarker using a collaborative generative adversarial networks (CollaGAN) model.
- To evaluate MRAβ's ability to mimic AV45 PET imaging and its diagnostic performance in distinguishing Alzheimer's disease and mild cognitive impairment from healthy controls.
Main Methods:
- Collected multimodal MRI and AV45 PET data from 380 participants in the ADNI dataset and 64 in the OASIS3 dataset.
- Applied a five-fold cross-validation CollaGAN model to generate MRAβ from multimodal MRI data.
- Utilized voxel-wise t-tests and a 3D ResNet classifier to assess MRAβ's accuracy and comparability to AV45.
Main Results:
- MRAβ successfully characterized subject-level AV45 spatial variations in AD and MCI patients.
- Amyloid-β depositions identified by MRAβ in AD and MCI were significantly higher than in healthy controls and highly correlated with AV45 findings (r > .92).
- MRAβ demonstrated comparable performance to AV45 in discriminating AD from healthy controls and MCI from healthy controls.
Conclusions:
- Multimodal MRI-derived MRAβ can effectively mimic cerebral amyloid-β depositions detected by AV45 PET imaging.
- MRAβ shows promise as a radiation-free, cost-effective molecular-explainable biomarker for Alzheimer's disease.
- This approach supports the advancement of MRI techniques for molecular biomarker applications in neurodegenerative diseases.
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