Cerebral Blood Flow Associations with Apolipoprotein E4 and Cerebral Amyloid Burden in Cognitively Intact Individuals
Motivation: Understanding how cerebral perfusion can inform mechanisms behind amyloid plaque accumulation, aiding early intervention strategies for Alzheimer's disease. Goal(s): To investigate the differences in cerebral perfusion in cognitively intact individuals with and without positive amyloid-PET and create a predictive model of amyloid plaque deposition. Approach: Utilizing neuroimaging techniques, we calculated cerebral perfusion metrics and compared them among amyloid positive vs negative individuals compensating for age, sex, APOE4 carriage and vascular comorbidities. Results: A predictive model that includes cerebral perfusion and APOE4 has increased sensitivity and specificity of amyloid burden prediction, proposing potential vascular targets for therapeutic interventions in neurodegeneration. Impact: Our results will impact researchers and clinicians, enhancing early Alzheimer's diagnosis and intervention. Future research may explore lifestyle and other vascular-targeting modifications for APOE4 carriers, allowing for personalized treatment strategies, and improving patient outcomes.
Authors
- Gina Dumkrieger (ORCID: https://orcid.org/0000-0001-9519-5370)
- Oana Dumitrașcu (ORCID: https://orcid.org/0000-0002-1031-9184)
- Leslie C. Baxter (ORCID: https://orcid.org/0000-0002-3971-863X)
- Bryan K. Woodruff (ORCID: https://orcid.org/0000-0002-4728-7294)
- Richard J. Caselli (ORCID: https://orcid.org/0000-0001-5784-2987)
- Simona Nikolova (ORCID: https://orcid.org/0000-0002-9203-1159)
Publication Details
- Journal
- Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
- Published
- 2025-09-16
- DOI
- https://doi.org/10.58530/2025/4575
- Primary Topic
- Neurological Disorders and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00