Novel imaging markers for altered cerebrovascular morphology in aging, stroke, and Alzheimer's disease
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Laksari_JON.pdf
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2023-07-15
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Final Accepted Manuscript
Author
Deshpande, AditiElliott, Jordan
Kari, Nitya
Jiang, Bin
Michel, Patrik
Toosizadeh, Nima
Fahadan, Pouya Tahsili
Kidwell, Chelsea
Wintermark, Max
Laksari, Kaveh
Affiliation
Department of Biomedical Engineering, University of ArizonaDepartment of Aerospace and Mechanical Engineering, University of Arizona
Issue Date
2022-07-15
Metadata
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WileyCitation
Deshpande, A., Elliott, J., Kari, N., Jiang, B., Michel, P., Toosizadeh, N., Fahadan, P. T., Kidwell, C., Wintermark, M., & Laksari, K. (2022). Novel imaging markers for altered cerebrovascular morphology in aging, stroke, and Alzheimer’s disease. Journal of Neuroimaging.Journal
Journal of NeuroimagingRights
© 2022 American Society of Neuroimaging.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Background and Purpose: Altered brain vasculature is a key phenomenon in several neurologic disorders. This paper presents a quantitative assessment of the anatomical variations in the Circle of Willis (CoW) and vascular morphology in healthy aging, acute ischemic stroke (AIS) and Alzheimer's Disease (AD). Methods: We used our novel automatic method to segment and extract geometric features of the cerebral vasculature from MR angiography scans of 175 healthy subjects, which were used to create a probabilistic atlas of cerebrovasculature and to study normal aging and intersubject variations in CoW anatomy. Subsequently, we quantified and analyzed vascular alterations in 45AIS and 50 AD patients, two prominent cerebrovascular and neurodegenerative disorders. Results: In the sampled cohort, we determined that the CoW is fully formed in only 35% of healthy adults and found significantly (p <.05) increased tortuosity and fractality, with increasing age and also with disease in both AIS and AD. We also found significantly lower vessel length, volume, and number of branches in AIS patients, as expected. The AD cerebral vessels exhibited significantly smaller diameter and more complex branching patterns, compared to age-matched healthy adults. These changes were significantly heightened (p <.05) among healthy, early onset mild AD, and moderate/severe dementia groups. Conclusion: Although our study does not include longitudinal data due to paucity of such datasets, the specific geometric features and quantitative comparisons demonstrate the potential for using vascular morphology as a noninvasive imaging biomarker for neurologic disorders.Note
12 month embargo; first published: 15 July 2022ISSN
1051-2284EISSN
1552-6569Version
Final accepted manuscriptae974a485f413a2113503eed53cd6c53
10.1111/jon.13023