UF1NS100599
Cooperative Agreement
Overview
Grant Description
Longitudinal Validation of Cerebral Small Vessel Disease Biomarkers in Diverse Community-Based Older Adults Without Dementia - Abstract
Cerebral small vessel disease (SVD) encompasses a range of common processes and pathologies (arteriolosclerosis, cerebral amyloid angiopathy, small vessel atherosclerosis, small and microscopic infarcts and bleeds, enlarged perivascular spaces, and white matter disease) that we and others have shown are associated with impaired cognition and dementia (VCID). High-quality biomarkers of SVD are critically needed to advance the diagnosis, prevention, and treatment of small vessel VCID.
The mission of the MARKVCID consortium has been to identify the most promising biomarkers of SVD and conduct analytical (instrumental) validation and preliminary clinical validation. Our team at Rush University Medical Center and Illinois Institute of Technology was privileged to be active participants in this initial work. We are now eager to continue this collaborative effort with this proposal.
The objective of the proposed project is to conduct rigorous longitudinal clinical validation of MARKVCID-selected biomarkers in a diverse cohort free of dementia, and to investigate the associations of these biomarkers with SVD neuropathologic indices, working synergistically with other consortium sites and contributing scientific expertise, experimental infrastructure, and scientific guidance.
Specifically, we propose to recruit, enroll, and longitudinally assess a large, diverse, community-based group of older adults without dementia using MARKVCID clinical evaluation and biomarkers, to test the hypotheses that the biomarkers are associated with cognitive decline and SVD neuropathologic indices.
This will be a nested sub-study of participants of the Rush Memory and Aging Project (MAP), Minority Aging Research Study (MARS), Religious Orders Study (ROS), Clinical Core (CC), and Latino Core (LATC) of the Rush Alzheimer's Disease Research Center, which are ongoing longitudinal, clinical-pathologic cohort studies of aging that recruit non-demented individuals and have high follow-up rates. MARS and CC recruit exclusively African Americans, and LATC recruits Latino older adults.
Our past contributions to MARKVCID support our current aims. First, we demonstrated our ability to recruit and follow a large and diverse group of non-demented older adults, some of whom died, enabling autopsy studies. Second, we developed and made publicly available a novel biomarker of arteriolosclerosis with high performance, named ARTS, which we trained using machine learning on MRI and pathology data. Third, we contributed to the analytical and initial clinical validation of multiple MARKVCID biomarkers. Fourth, we led the MARKVCID imaging biomarkers committee and were active in all functions of the consortium.
We propose to leverage our expertise and infrastructure to conduct rigorous longitudinal clinical validation of MARKVCID biomarkers in a diverse population, and to investigate the associations of these biomarkers with SVD neuropathologic indices.
Cerebral small vessel disease (SVD) encompasses a range of common processes and pathologies (arteriolosclerosis, cerebral amyloid angiopathy, small vessel atherosclerosis, small and microscopic infarcts and bleeds, enlarged perivascular spaces, and white matter disease) that we and others have shown are associated with impaired cognition and dementia (VCID). High-quality biomarkers of SVD are critically needed to advance the diagnosis, prevention, and treatment of small vessel VCID.
The mission of the MARKVCID consortium has been to identify the most promising biomarkers of SVD and conduct analytical (instrumental) validation and preliminary clinical validation. Our team at Rush University Medical Center and Illinois Institute of Technology was privileged to be active participants in this initial work. We are now eager to continue this collaborative effort with this proposal.
The objective of the proposed project is to conduct rigorous longitudinal clinical validation of MARKVCID-selected biomarkers in a diverse cohort free of dementia, and to investigate the associations of these biomarkers with SVD neuropathologic indices, working synergistically with other consortium sites and contributing scientific expertise, experimental infrastructure, and scientific guidance.
Specifically, we propose to recruit, enroll, and longitudinally assess a large, diverse, community-based group of older adults without dementia using MARKVCID clinical evaluation and biomarkers, to test the hypotheses that the biomarkers are associated with cognitive decline and SVD neuropathologic indices.
This will be a nested sub-study of participants of the Rush Memory and Aging Project (MAP), Minority Aging Research Study (MARS), Religious Orders Study (ROS), Clinical Core (CC), and Latino Core (LATC) of the Rush Alzheimer's Disease Research Center, which are ongoing longitudinal, clinical-pathologic cohort studies of aging that recruit non-demented individuals and have high follow-up rates. MARS and CC recruit exclusively African Americans, and LATC recruits Latino older adults.
Our past contributions to MARKVCID support our current aims. First, we demonstrated our ability to recruit and follow a large and diverse group of non-demented older adults, some of whom died, enabling autopsy studies. Second, we developed and made publicly available a novel biomarker of arteriolosclerosis with high performance, named ARTS, which we trained using machine learning on MRI and pathology data. Third, we contributed to the analytical and initial clinical validation of multiple MARKVCID biomarkers. Fourth, we led the MARKVCID imaging biomarkers committee and were active in all functions of the consortium.
We propose to leverage our expertise and infrastructure to conduct rigorous longitudinal clinical validation of MARKVCID biomarkers in a diverse population, and to investigate the associations of these biomarkers with SVD neuropathologic indices.
Awardee
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Funding Agency
Place of Performance
Chicago,
Illinois
606123833
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have decreased 43% from $2,472,997 to $1,417,802.
Rush University Medical Center was awarded
Longitudinal Validation of SVD Biomarkers in Diverse Older Adults
Cooperative Agreement UF1NS100599
worth $1,417,802
from National Institute on Aging in September 2016 with work to be completed primarily in Chicago Illinois United States.
The grant
has a duration of 6 years 10 months and
was awarded through assistance program 93.866 Aging Research.
The Cooperative Agreement was awarded through grant opportunity Small Vessel VCID Biomarker Validation Consortium Sites (U01)(Clinical Trials Not Allowed).
Status
(Complete)
Last Modified 3/20/24
Period of Performance
9/1/16
Start Date
7/31/23
End Date
Funding Split
$1.4M
Federal Obligation
$0.0
Non-Federal Obligation
$1.4M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for UF1NS100599
Transaction History
Modifications to UF1NS100599
Additional Detail
Award ID FAIN
UF1NS100599
SAI Number
UF1NS100599-761045737
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Nonprofit With 501(c)(3) IRS Status (Other Than An Institution Of Higher Education)
Awarding Office
75NQ00 NIH NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
Funding Office
75NN00 NIH NATIONAL INSITUTE ON AGING
Awardee UEI
C155UU2TXCP3
Awardee CAGE
3F752
Performance District
IL-07
Senators
Richard Durbin
Tammy Duckworth
Tammy Duckworth
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Institute on Aging, National Institutes of Health, Health and Human Services (075-0843) | Health research and training | Grants, subsidies, and contributions (41.0) | $1,013,102 | 100% |
Modified: 3/20/24