Title project: ?leptomeningeal vessel wall enhancement as an early pathophysiological marker of cerebral amyloid angiopathy? Cerebral amyloid angiopathy (CAA) is a significant contributor to cognitive impairment and dementia and a leading cause of intracerebral hemorrhage (ICH) in older individuals. CAA is characterized by the accumulation of A? in the walls of cortical and leptomeningeal vessels. It has been suggested that vascular A? deposition involves a self-reinforcing cycle of reduced vascular reactivity and impaired perivascular clearance of A? from the brain, eventually resulting in vessel wall breakdown and the formation of hemorrhages. Currently, CAA patients are only recognized during the late stages of the disease by the detection of hemorrhages on brain MRI. Bleeding from leptomeningeal vessels, recognized as superficial siderosis on MRI, has recently emerged as one of the strongest predictors for future symptomatic ICH. However, there are currently no in vivo tools available to identify vessels at risk for superficial siderosis. In this proposal, we aim to determine the potential of contrast agent leakage as an early detection strategy to predict future sites of bleeding. We will utilize high-resolution heavily T2-weighted post-contrast fluid-attenuated inversion recovery (FLAIR) MRI after intravenous gadolinium administration to detect leakage from individual leptomeningeal vessels at the surface of the brain. Leveraging the dataset acquired in this patient population, we will further assess the clearance of gadolinium after focal leakage into perivascular spaces to determine the feasibility of mapping perivascular clearance routes in humans non-invasively. The results will inform the design of future mechanistic studies looking at perivascular clearance dynamics in CAA and Alzheimer?s disease. The proposal builds on the applicants? international leadership in CAA, their strong background in advanced neuroimaging, and translational research program involving ex vivo MRI-guided neuropathology and in vivo two-photon imaging in mouse models. Combined with the world-class resources and international collaborations with experts in the field to perform advanced image processing, the proposed set of experiments will likely yield much needed answers regarding the early pathophysiology in CAA. Novel insights resulting from this project may also yield promising new targets to prevent vascular cognitive impairment and dementia in the elderly.

Public Health Relevance

The proposed research aims to determine the potential of contrast agent leakage as an early detection strategy to identify vessel wall breakdown in patients with cerebral amyloid angiopathy with the goal to predict future sites of bleeding. In addition, leveraging post-contrast neuroimaging data in this patient population we will study clearance of gadolinium within perivascular spaces after focal leakage. The results will inform the design of future mechanistic studies into perivascular A? clearance, which plays an important role in the early pathophysiology of cerebral amyloid angiopathy and Alzheimer?s disease.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AG070363-01
Application #
10108743
Study Section
Acute Neural Injury and Epilepsy Study Section (ANIE)
Program Officer
Hsiao, John
Project Start
2020-09-15
Project End
2022-08-31
Budget Start
2020-09-15
Budget End
2022-08-31
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02114