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Active NON-SBIR/STTR RPGS NIH (US)

Vascular Imaging Biomarker Relationships to Alzheimer’s disease (VIBRA)

$7.9M USD

Funder NATIONAL INSTITUTE ON AGING
Recipient Organization University of Texas Hlth Science Center
Country United States
Start Date Sep 15, 2024
End Date May 31, 2029
Duration 1,719 days
Number of Grantees 2
Roles Principal Investigator; Co-Investigator
Data Source NIH (US)
Grant ID 10885322
Grant Description

PROJECT SUMMARY / ABSTRACT Improving vascular health is a potential strategy to delay the onset of Alzheimer's disease (AD) and related dementias (ADRD). The overlap of cerebral small vessel disease (SVD) and AD pathology may be the most common neuropathologic phenotype of age-related dementia. However, rarely do imaging studies of ADRD

include measures of SVD commonly observed on brain MRI scans in older adults. Due to challenges in quantification in large cohort studies, manual reads are typically done; these are very time-consuming, prone to human error, and lack spatial anatomic resolution. This distinction is most apparent in the Clinical Core studies

of NIH-funded Alzheimer's Disease Research Centers (ADRCs), where SVD biomarkers are technically challenging, time-consuming, and often overlooked. Filling this critical gap will require technologies to robustly identify SVD lesions on brain MRI. Recent technological advances make computerized SVD biomarkers

possible, reproducible, and feasible for large cohorts. Using various MRI pulse sequences, we have developed novel deep-learning methods to accurately quantify SVD biomarkers, including cerebral microbleeds, white matter hyperintensities, and enlarged perivascular spaces. These reading methods are reliable and offer greater

anatomic precision and dynamic range than previous scoring systems. Thus, our primary aim is to create an inter-ADRC set of objectively measured SVD MRI biomarkers from large and diverse clinical cohorts to determine the role of SVD in vascular contributions to ADRD. These ADRCs include 4,831 (49% minority) individuals at

risk for ADRD. We will use the rich clinical and neuroimaging (structural MRI) data within the South Texas, Wake Forest, Wisconsin, and the University of California Davis ADRCs and their affiliated cohorts, including the Vascular Contributions to Cognitive Impairment and Dementia consortium, the Multi-Ethnic Study of

Atherosclerosis, and The Wisconsin Registry for Alzheimer's Prevention to address unanswered questions related to the contribution of SVD to ADRD. We will apply our deep learning models to address the following Specific Aims: 1) Standardize quantification of cerebral SVD markers in diverse cohorts to allow objective

readings from neuroimaging data currently missing in the ADRCs. 2) Relate cerebral SVD lesions with clinical cognitive staging, ADRD neuroimaging, and biofluid biomarkers in diverse ADRC cohorts. 3) Explore vascular and metabolic pathways linking SVD to worse cognition and longitudinal cognitive decline in the context of ADRD

biomarkers. Further, we will share our robust machine learning models and implementation software with the scientific community. This foundational work will produce and validate computerized methods for SVD characterization and build a much-needed resource to assess vascular contributions to cognitive impairment in

AD/ADRD research in under-represented populations. Furthermore, this project will provide evidence for reproducible and harmonized SVD outcomes critical to understanding the complexity of ADRD for adoption by ADRC MRI research studies, which would be scalable with future grant-supported initiatives.

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All Grantees

University of Texas Hlth Science Center

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