Novel imaging markers for altered cerebrovascular morphology in aging, stroke, and Alzheimer's disease.


Journal

Journal of neuroimaging : official journal of the American Society of Neuroimaging
ISSN: 1552-6569
Titre abrégé: J Neuroimaging
Pays: United States
ID NLM: 9102705

Informations de publication

Date de publication:
09 2022
Historique:
revised: 26 06 2022
received: 08 02 2022
accepted: 29 06 2022
pubmed: 16 7 2022
medline: 14 9 2022
entrez: 15 7 2022
Statut: ppublish

Résumé

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). 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. 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. 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.

Sections du résumé

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.

Identifiants

pubmed: 35838658
doi: 10.1111/jon.13023
pmc: PMC9474631
mid: NIHMS1820592
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

956-967

Subventions

Organisme : NINDS NIH HHS
ID : R03 NS108167
Pays : United States
Organisme : NIBIB NIH HHS
ID : R21 EB032187
Pays : United States

Informations de copyright

© 2022 American Society of Neuroimaging.

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Auteurs

Aditi Deshpande (A)

Department of Biomedical Engineering, University of Arizona, Tucson, Arizona, USA.

Jordan Elliott (J)

Department of Biomedical Engineering, University of Arizona, Tucson, Arizona, USA.

Nitya Kari (N)

Department of Biomedical Engineering, University of Arizona, Tucson, Arizona, USA.

Bin Jiang (B)

Department of Radiology, Stanford University, Stanford, California, USA.

Patrik Michel (P)

Department of Neurology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

Nima Toosizadeh (N)

Department of Biomedical Engineering, University of Arizona, Tucson, Arizona, USA.
Arizona Center on Aging, Department of Medicine, University of Arizona, Tucson, Arizona, USA.

Pouya Tahsili Fahadan (PT)

Neuroscience Intensive Care Unit, Medical Critical Care Service and Department of Medical Education, UVA Medicine Inova Campus, Falls Church, Virginia, USA.
Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Chelsea Kidwell (C)

Department of Neurology, University of Arizona, Tucson, Arizona, USA.

Max Wintermark (M)

Department of Neuroradiology, MD Anderson Center, University of Texas, Houston, Texas, USA.

Kaveh Laksari (K)

Department of Biomedical Engineering, University of Arizona, Tucson, Arizona, USA.
Department of Aerospace and Mechanical Engineering, University of Arizona, Tucson, Arizona, USA.

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