R01HL157220
Project Grant
Overview
Grant Description
Intradialytic Myocardial Stunning in Hemodialysis Patients - A Novel Cardiovascular Risk Factor
Despite rigorous investigations and the expenditure of nearly 6% of Medicare funds on their care, annual mortality among the 511,000 dialysis patients in the United States is extraordinarily high. Approximately, 17% of patients die annually with half of deaths attributable to cardiovascular (CV) causes, particularly sudden cardiac death. Current therapies do not effectively lower CV mortality in hemodialysis (HD) patients, thus highlighting the importance of addressing existing gaps in understanding the mechanisms underlying CV complications in HD patients and identifying novel therapeutic targets.
Transient intra-dialytic myocardial stunning (IDMS) during HD—the dominant dialysis modality in the US—has been increasingly implicated as one such mechanism potentially responsible for progressive myocardial damage and subsequent development of heart failure, arrhythmia, and CV death. However, current understanding of this novel risk factor is woefully incomplete. Prior studies were small, included few women, non-white, or incident patients—those with the highest risk of CV death—and variation in estimated prevalence was extreme (20-100%). In addition, studies of IDMS risk factors were underpowered and conflicting, and it remains unknown whether IDMS occurs intermittently or repetitively. Finally, although our both our own preliminary data and studies by other groups implicate a potential role for autonomic dysfunction in IDMS pathophysiology, there have been few mechanistic investigations and understanding of the underlying pathophysiology is incomplete.
In short, IDMS is a potentially important and treatable contributor to CV death in the HD population, but there are major gaps in understanding its epidemiology, risk factors, and mechanisms. We propose studies designed to address these critical knowledge gaps and provide the necessary information to determine whether and how IDMS should be targeted to reduce CV mortality in HD:
In Aim 1, we propose performing intradialytic echocardiography on a large, diverse cohort of 400 incident HD patients to facilitate stable, generalizable estimates of IDMS prevalence, the analysis of important subgroups, and the study of associations with key risk factors.
In Aim 2, we propose a comprehensive investigation of the hypothesis that unopposed surges in sympathetic tone underlie susceptibility to IDMS. Myocardial 11C-hydroxyephedrine PET scanning and dedicated studies in an autonomic function lab will be utilized to assess systematic and myocardial-specific autonomic function. Conversely, intradialytic autonomic tone and circulating hormones will be measured during dialysis to systematically define the patterns of change in autonomic tone preceding and predisposing to episodes of IDMS.
These studies will improve understanding of the epidemiology and physiology of a potentially critical contributor to cardiovascular morbidity and mortality in the dialysis population, improve basic understanding of the pathophysiologic impact of HD on the heart, and provide the necessary data to design targeted therapeutics to reduce CV death for high-risk patients.
Despite rigorous investigations and the expenditure of nearly 6% of Medicare funds on their care, annual mortality among the 511,000 dialysis patients in the United States is extraordinarily high. Approximately, 17% of patients die annually with half of deaths attributable to cardiovascular (CV) causes, particularly sudden cardiac death. Current therapies do not effectively lower CV mortality in hemodialysis (HD) patients, thus highlighting the importance of addressing existing gaps in understanding the mechanisms underlying CV complications in HD patients and identifying novel therapeutic targets.
Transient intra-dialytic myocardial stunning (IDMS) during HD—the dominant dialysis modality in the US—has been increasingly implicated as one such mechanism potentially responsible for progressive myocardial damage and subsequent development of heart failure, arrhythmia, and CV death. However, current understanding of this novel risk factor is woefully incomplete. Prior studies were small, included few women, non-white, or incident patients—those with the highest risk of CV death—and variation in estimated prevalence was extreme (20-100%). In addition, studies of IDMS risk factors were underpowered and conflicting, and it remains unknown whether IDMS occurs intermittently or repetitively. Finally, although our both our own preliminary data and studies by other groups implicate a potential role for autonomic dysfunction in IDMS pathophysiology, there have been few mechanistic investigations and understanding of the underlying pathophysiology is incomplete.
In short, IDMS is a potentially important and treatable contributor to CV death in the HD population, but there are major gaps in understanding its epidemiology, risk factors, and mechanisms. We propose studies designed to address these critical knowledge gaps and provide the necessary information to determine whether and how IDMS should be targeted to reduce CV mortality in HD:
In Aim 1, we propose performing intradialytic echocardiography on a large, diverse cohort of 400 incident HD patients to facilitate stable, generalizable estimates of IDMS prevalence, the analysis of important subgroups, and the study of associations with key risk factors.
In Aim 2, we propose a comprehensive investigation of the hypothesis that unopposed surges in sympathetic tone underlie susceptibility to IDMS. Myocardial 11C-hydroxyephedrine PET scanning and dedicated studies in an autonomic function lab will be utilized to assess systematic and myocardial-specific autonomic function. Conversely, intradialytic autonomic tone and circulating hormones will be measured during dialysis to systematically define the patterns of change in autonomic tone preceding and predisposing to episodes of IDMS.
These studies will improve understanding of the epidemiology and physiology of a potentially critical contributor to cardiovascular morbidity and mortality in the dialysis population, improve basic understanding of the pathophysiologic impact of HD on the heart, and provide the necessary data to design targeted therapeutics to reduce CV death for high-risk patients.
Awardee
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
New York,
New York
100169196
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 367% from $740,651 to $3,460,403.
New York University was awarded
IDMS in Hemodialysis Patients: Novel Cardiovascular Risk Factor Study
Project Grant R01HL157220
worth $3,460,403
from National Heart Lung and Blood Institute in December 2021 with work to be completed primarily in New York New York United States.
The grant
has a duration of 5 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 5/21/26
Period of Performance
12/24/21
Start Date
11/30/26
End Date
Funding Split
$3.5M
Federal Obligation
$0.0
Non-Federal Obligation
$3.5M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01HL157220
Transaction History
Modifications to R01HL157220
Additional Detail
Award ID FAIN
R01HL157220
SAI Number
R01HL157220-3695998072
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
M5SZJ6VHUHN8
Awardee CAGE
3D476
Performance District
NY-12
Senators
Kirsten Gillibrand
Charles Schumer
Charles Schumer
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) | $1,433,316 | 100% |
Modified: 5/21/26