R01HL159987
Project Grant
Overview
Grant Description
Interplay of Myocardial Fibrosis and Cardiac TTR Amyloid in Age-Related Cardiac Remodeling in MESA-Multi-Ethnic Study of Atherosclerosis - Project Summary:
Myocardial fibrosis is characterized by the accumulation of extracellular matrix in the myocardium and has been identified as one of the main determinants of age-related cardiac remodeling. This can manifest as either increased diffuse interstitial fibrosis or focal fibrosis as a scar and lead to cardiac dysfunction. On the other hand, cardiac transthyretin amyloidosis, characterized by infiltration of the myocardium by misfolded transthyretin protein, has emerged as an important cause of accelerated remodeling leading to heart failure and cardiovascular disease (CVD), and predisposing to frailty and dementia. Importantly, novel FDA-approved therapies (tafamidis, inotersen) may allow treatment of cardiac amyloidosis, highlighting the need for early detection.
We expect this study to establish the pivotal importance of quantifying fibrosis and amyloidosis at the population level to facilitate clinical detection and orient the development of novel strategies to prevent heart failure, atrial fibrillation, and complications of CVD in older adults. Therefore, our specific aims are:
Aim 1A) Determine the cross-sectional associations of presence as well as extent of amyloidosis measured by TC-PYP, with extent of myocardial fibrosis measured by MRI T1 mapping at MESA Exam 7.
1B) Determine cross-sectional associations of presence and extent of amyloidosis as well as fibrosis, with magnitude of cardiac remodeling defined as structural and functional alterations of the left and right heart chambers by cine MRI at MESA Exam 7.
1C) Construct prediction models for presence as well as for extent of both cardiac amyloidosis and progressive fibrosis at Exam 7, by combining risk factor exposure and subclinical disease trajectories based on phenotypes obtained from all MESA Exams (1-6) prior to Exam 7.
In Aim 2A) we will compare the magnitude of ECV change between MESA Exams 5 and 7 in the absence versus presence, as well as extent of amyloidosis measured at Exam 7.
2B) Compare the magnitude of 12-14 year changes in 4 chamber cardiac remodeling attributed to amyloidosis versus those attributed to progressive fibrosis.
2C) Construct longitudinal predictive models of 12-14 year change in ECV attributed to amyloidosis versus ECV changes attributed to progressive fibrosis, using all phenotypic variables obtained from MESA Exams 1 through 5.
We propose to use data acquired during 2010-2012 in 800 individuals (400 men and 400 women) as part of the MESA 5 Exam. As part of this proposal, all participants will undergo a repeat MRI exam and TC-99m-PYP at Exam 7. This study leverages the already acquired MESA phenotypic data to predict amyloidosis and malignant progressive fibrosis leading to adverse remodeling, CVD, frailty, and dementia.
Myocardial fibrosis is characterized by the accumulation of extracellular matrix in the myocardium and has been identified as one of the main determinants of age-related cardiac remodeling. This can manifest as either increased diffuse interstitial fibrosis or focal fibrosis as a scar and lead to cardiac dysfunction. On the other hand, cardiac transthyretin amyloidosis, characterized by infiltration of the myocardium by misfolded transthyretin protein, has emerged as an important cause of accelerated remodeling leading to heart failure and cardiovascular disease (CVD), and predisposing to frailty and dementia. Importantly, novel FDA-approved therapies (tafamidis, inotersen) may allow treatment of cardiac amyloidosis, highlighting the need for early detection.
We expect this study to establish the pivotal importance of quantifying fibrosis and amyloidosis at the population level to facilitate clinical detection and orient the development of novel strategies to prevent heart failure, atrial fibrillation, and complications of CVD in older adults. Therefore, our specific aims are:
Aim 1A) Determine the cross-sectional associations of presence as well as extent of amyloidosis measured by TC-PYP, with extent of myocardial fibrosis measured by MRI T1 mapping at MESA Exam 7.
1B) Determine cross-sectional associations of presence and extent of amyloidosis as well as fibrosis, with magnitude of cardiac remodeling defined as structural and functional alterations of the left and right heart chambers by cine MRI at MESA Exam 7.
1C) Construct prediction models for presence as well as for extent of both cardiac amyloidosis and progressive fibrosis at Exam 7, by combining risk factor exposure and subclinical disease trajectories based on phenotypes obtained from all MESA Exams (1-6) prior to Exam 7.
In Aim 2A) we will compare the magnitude of ECV change between MESA Exams 5 and 7 in the absence versus presence, as well as extent of amyloidosis measured at Exam 7.
2B) Compare the magnitude of 12-14 year changes in 4 chamber cardiac remodeling attributed to amyloidosis versus those attributed to progressive fibrosis.
2C) Construct longitudinal predictive models of 12-14 year change in ECV attributed to amyloidosis versus ECV changes attributed to progressive fibrosis, using all phenotypic variables obtained from MESA Exams 1 through 5.
We propose to use data acquired during 2010-2012 in 800 individuals (400 men and 400 women) as part of the MESA 5 Exam. As part of this proposal, all participants will undergo a repeat MRI exam and TC-99m-PYP at Exam 7. This study leverages the already acquired MESA phenotypic data to predict amyloidosis and malignant progressive fibrosis leading to adverse remodeling, CVD, frailty, and dementia.
Awardee
Funding Goals
TO FOSTER HEART AND VASCULAR RESEARCH IN THE BASIC, TRANSLATIONAL, CLINICAL AND POPULATION SCIENCES, AND TO FOSTER TRAINING TO BUILD TALENTED YOUNG INVESTIGATORS IN THESE AREAS, FUNDED THROUGH COMPETITIVE RESEARCH TRAINING GRANTS. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, USE SMALL BUSINESS TO MEET FEDERAL RESEARCH AND DEVELOPMENT NEEDS, FOSTER AND ENCOURAGE PARTICIPATION IN INNOVATION AND ENTREPRENEURSHIP BY SOCIALLY AND ECONOMICALLY DISADVANTAGED PERSONS, AND INCREASE PRIVATE-SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT FUNDING. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, FOSTER TECHNOLOGY TRANSFER THROUGH COOPERATIVE R&D BETWEEN SMALL BUSINESSES AND RESEARCH INSTITUTIONS, AND INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL R&D.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Baltimore,
Maryland
212051832
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 280% from $1,461,844 to $5,552,808.
The Johns Hopkins University was awarded
Cardiac Fibrosis & Amyloidosis in Age-Related Remodeling - MESA Study
Project Grant R01HL159987
worth $5,552,808
from National Heart Lung and Blood Institute in April 2022 with work to be completed primarily in Baltimore Maryland United States.
The grant
has a duration of 4 years and
was awarded through assistance program 93.837 Cardiovascular Diseases Research.
The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 7/3/25
Period of Performance
4/1/22
Start Date
3/31/26
End Date
Funding Split
$5.6M
Federal Obligation
$0.0
Non-Federal Obligation
$5.6M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01HL159987
Transaction History
Modifications to R01HL159987
Additional Detail
Award ID FAIN
R01HL159987
SAI Number
R01HL159987-3698405568
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Private Institution Of Higher Education
Awarding Office
75NH00 NIH National Heart, Lung, and Blood Institute
Funding Office
75NH00 NIH National Heart, Lung, and Blood Institute
Awardee UEI
FTMTDMBR29C7
Awardee CAGE
5L406
Performance District
MD-07
Senators
Benjamin Cardin
Chris Van Hollen
Chris Van Hollen
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Heart, Lung, and Blood Institute, National Institutes of Health, Health and Human Services (075-0872) | Health research and training | Grants, subsidies, and contributions (41.0) | $2,840,478 | 100% |
Modified: 7/3/25