R01NS123734
Project Grant
Overview
Grant Description
Platelet Expression of FcγRIIA and Arterial Hemodynamics to Predict Recurrent Stroke in Intracranial Atherosclerosis - Project Summary/Abstract
The overall goal of this proposal is to determine the potentially pivotal and interactive roles of individual platelet expression of FcγRIIA and wall shear stress (WSS) calculated from patient-specific CT angiography (CTA) computational fluid dynamics (CFD) to explain recurrent ischemia after minor stroke or TIA due to ICAD. A precision model is developed to quantify the risk of recurrent ischemic injury, accounting for FcγRIIA, WSS, anti-platelet therapies, and platelet reactivity, across a diverse population of stroke and TIA patients with ICAD.
Our central hypothesis is that high FcγRIIA plus high shear force pose individual and synergistic risk of stroke recurrence, providing a rational basis for the precision medicine of stroke prevention in ICAD. Our preliminary data reveal that greater platelet FcγRIIA expression identifies patients at greater risk of recurrent cardiovascular events, including stroke, and that high WSS on CTA CFD predicts recurrent stroke due to ICAD at 1 year.
Our three independent specific aims leverage an established research infrastructure and ICAD network of 6 geographically distinct enrolling sites with race-ethnic diverse populations and a longstanding history of productive collaboration to recruit 250 participants with acute cerebral ischemia within 72 hours from symptom onset. The multicenter, observational study will enroll stroke or TIA patients due to 50-99% ICAD diagnosed on routinely acquired CTA and obtain brain MRI and blood sampling for FcγRIIA and platelet assays within 72 hours and again at 1 year after onset. Clinical outcomes will be ascertained at 90 days and at 1 year, with co-registration of serial MRI to quantify interval silent and symptomatic ischemic injury.
The Platelet Biology Core at the University of Vermont will quantify platelet FcγRIIA expression. The Neurovascular Imaging Research Core at UCLA will conduct central imaging analyses, including CTA CFD quantification of WSS, serial MRI co-registration, and imaging adjudication of eligibility and interval endpoints. The Statistical Core will coordinate data management from 6 enrolling sites and the core facilities, conducting predictive statistics, stratification of key biological variables, and novel application of clustering analytic strategies to maximally inform a precision model of ICAD stroke risk at 1 year.
This timely culmination of synergistic work on shear stress-induced platelet activation in ICAD leverages our robust preliminary data on FcγRIIA, CTA CFD of WSS, and precision medicine analytics in stroke, layered on a successful track record of multicenter, observational studies of the most common cause of recurrent stroke. Measurement of individual differences in FcγRIIA and shear stress induced by heterogeneous arterial stenoses inform a logical precision medicine strategy to avert stroke. This novel strategy of using diagnostic data easily acquired shortly after stroke or TIA due to ICAD has clear implications for clinical translation via precision medicine, enabling individualized stroke treatment focused on mechanisms of platelet pathophysiology while addressing clinical events and silent, insidious brain damage due to recurrent ischemia distal to the plaque.
The overall goal of this proposal is to determine the potentially pivotal and interactive roles of individual platelet expression of FcγRIIA and wall shear stress (WSS) calculated from patient-specific CT angiography (CTA) computational fluid dynamics (CFD) to explain recurrent ischemia after minor stroke or TIA due to ICAD. A precision model is developed to quantify the risk of recurrent ischemic injury, accounting for FcγRIIA, WSS, anti-platelet therapies, and platelet reactivity, across a diverse population of stroke and TIA patients with ICAD.
Our central hypothesis is that high FcγRIIA plus high shear force pose individual and synergistic risk of stroke recurrence, providing a rational basis for the precision medicine of stroke prevention in ICAD. Our preliminary data reveal that greater platelet FcγRIIA expression identifies patients at greater risk of recurrent cardiovascular events, including stroke, and that high WSS on CTA CFD predicts recurrent stroke due to ICAD at 1 year.
Our three independent specific aims leverage an established research infrastructure and ICAD network of 6 geographically distinct enrolling sites with race-ethnic diverse populations and a longstanding history of productive collaboration to recruit 250 participants with acute cerebral ischemia within 72 hours from symptom onset. The multicenter, observational study will enroll stroke or TIA patients due to 50-99% ICAD diagnosed on routinely acquired CTA and obtain brain MRI and blood sampling for FcγRIIA and platelet assays within 72 hours and again at 1 year after onset. Clinical outcomes will be ascertained at 90 days and at 1 year, with co-registration of serial MRI to quantify interval silent and symptomatic ischemic injury.
The Platelet Biology Core at the University of Vermont will quantify platelet FcγRIIA expression. The Neurovascular Imaging Research Core at UCLA will conduct central imaging analyses, including CTA CFD quantification of WSS, serial MRI co-registration, and imaging adjudication of eligibility and interval endpoints. The Statistical Core will coordinate data management from 6 enrolling sites and the core facilities, conducting predictive statistics, stratification of key biological variables, and novel application of clustering analytic strategies to maximally inform a precision model of ICAD stroke risk at 1 year.
This timely culmination of synergistic work on shear stress-induced platelet activation in ICAD leverages our robust preliminary data on FcγRIIA, CTA CFD of WSS, and precision medicine analytics in stroke, layered on a successful track record of multicenter, observational studies of the most common cause of recurrent stroke. Measurement of individual differences in FcγRIIA and shear stress induced by heterogeneous arterial stenoses inform a logical precision medicine strategy to avert stroke. This novel strategy of using diagnostic data easily acquired shortly after stroke or TIA due to ICAD has clear implications for clinical translation via precision medicine, enabling individualized stroke treatment focused on mechanisms of platelet pathophysiology while addressing clinical events and silent, insidious brain damage due to recurrent ischemia distal to the plaque.
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Los Angeles,
California
900890146
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 370% from $712,730 to $3,350,551.
University Of Southern California was awarded
Platelet FcγRIIA & Arterial Hemodynamics: Predicting Stroke Recurrence in ICAD
Project Grant R01NS123734
worth $3,350,551
from the National Institute of Neurological Disorders and Stroke in April 2022 with work to be completed primarily in Los Angeles California United States.
The grant
has a duration of 5 years and
was awarded through assistance program 93.853 Extramural Research Programs in the Neurosciences and Neurological Disorders.
The Project Grant was awarded through grant opportunity Change of Recipient Organization (Type 7 Parent Clinical Trial Optional).
Status
(Ongoing)
Last Modified 5/21/26
Period of Performance
4/1/22
Start Date
3/31/27
End Date
Funding Split
$3.4M
Federal Obligation
$0.0
Non-Federal Obligation
$3.4M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01NS123734
Transaction History
Modifications to R01NS123734
Additional Detail
Award ID FAIN
R01NS123734
SAI Number
R01NS123734-3104639361
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Private Institution Of Higher Education
Awarding Office
75NQ00 NIH National Institute of Neurological Disorders and Stroke
Funding Office
75NQ00 NIH National Institute of Neurological Disorders and Stroke
Awardee UEI
G88KLJR3KYT5
Awardee CAGE
1B729
Performance District
CA-34
Senators
Dianne Feinstein
Alejandro Padilla
Alejandro Padilla
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Institute of Neurological Disorders and Stroke, National Institutes of Health, Health and Human Services (075-0886) | Health research and training | Grants, subsidies, and contributions (41.0) | $1,344,900 | 100% |
Modified: 5/21/26