R01AG084710
Project Grant
Overview
Grant Description
Epigenetics biomarker of post operative delirium and long term cognitive decline among elderly dementia patients - Project summary/abstract
Delirium exposes patients to a greater risk of developing Alzheimer’s disease and dementia, and patients with Alzheimer’s disease and dementia are more likely to develop delirium.
Delirium among elderly patients is dangerous and common, yet it is underdiagnosed and undertreated.
Especially common in patients with Alzheimer’s disease, delirium is a strong predictor of poor outcomes including post-operative cognitive decline (POCD) and mortality.
The key to reducing the burden associated with delirium is early identification of those at high risk for it, especially prior to surgery, which is known to be a major risk factor for delirium.
However, currently, there are no reliable tools available to predict the risk of post-operative delirium (POD).
Also, there is no clear understanding of the pathophysiological mechanism of delirium.
The long-term goal of this project is to investigate the role of epigenetics to better understand the molecular mechanism of pathogenesis of POD and to identify potential biomarkers associated with POD and POCD.
We will test for a specific type of epigenetic modification, DNA methylation (DNAM), which is known to be induced by environmental factors.
Previous searches for biomarkers of delirium in humans led to the proposal that inflammation and pro-inflammatory cytokines play a key role in the pathophysiology of delirium.
Yet, how the aging process enhances cytokine release remains unclear.
Aging is known to have a strong effect on gene expression, and such changes in gene expression are tightly controlled by DNAM.
Thus, it is suspected that DNAM changes over the course of aging, leading to enhanced cytokine release due to altered control of gene expression, and that such DNAM modification contributes to delirium.
This project will be the first to investigate the role of epigenetics associated with POD in humans, and the objective of the project is to identify potential biomarkers for elevated risk of POD and subsequent patient outcomes related to delirium such as POCD and dementia.
The proposed research will accomplish its objective by following a large sample of elderly patients going through hip fracture surgery throughout their hospital stay, comparing differences in genome-wide DNAM between those who develop POD and those who do not.
Lastly, the project will test if DNAM is predictive of patient outcomes including survival and long-term memory problems after surgery.
This research will enhance our understanding of the epigenetic mechanisms in the pathogenesis of delirium and its interplay with the progression of dementia, and may identify biomarkers predictive of their risk.
The identification of epigenetic markers of delirium would hopefully lead to improvement in medical and surgical practice.
Delirium exposes patients to a greater risk of developing Alzheimer’s disease and dementia, and patients with Alzheimer’s disease and dementia are more likely to develop delirium.
Delirium among elderly patients is dangerous and common, yet it is underdiagnosed and undertreated.
Especially common in patients with Alzheimer’s disease, delirium is a strong predictor of poor outcomes including post-operative cognitive decline (POCD) and mortality.
The key to reducing the burden associated with delirium is early identification of those at high risk for it, especially prior to surgery, which is known to be a major risk factor for delirium.
However, currently, there are no reliable tools available to predict the risk of post-operative delirium (POD).
Also, there is no clear understanding of the pathophysiological mechanism of delirium.
The long-term goal of this project is to investigate the role of epigenetics to better understand the molecular mechanism of pathogenesis of POD and to identify potential biomarkers associated with POD and POCD.
We will test for a specific type of epigenetic modification, DNA methylation (DNAM), which is known to be induced by environmental factors.
Previous searches for biomarkers of delirium in humans led to the proposal that inflammation and pro-inflammatory cytokines play a key role in the pathophysiology of delirium.
Yet, how the aging process enhances cytokine release remains unclear.
Aging is known to have a strong effect on gene expression, and such changes in gene expression are tightly controlled by DNAM.
Thus, it is suspected that DNAM changes over the course of aging, leading to enhanced cytokine release due to altered control of gene expression, and that such DNAM modification contributes to delirium.
This project will be the first to investigate the role of epigenetics associated with POD in humans, and the objective of the project is to identify potential biomarkers for elevated risk of POD and subsequent patient outcomes related to delirium such as POCD and dementia.
The proposed research will accomplish its objective by following a large sample of elderly patients going through hip fracture surgery throughout their hospital stay, comparing differences in genome-wide DNAM between those who develop POD and those who do not.
Lastly, the project will test if DNAM is predictive of patient outcomes including survival and long-term memory problems after surgery.
This research will enhance our understanding of the epigenetic mechanisms in the pathogenesis of delirium and its interplay with the progression of dementia, and may identify biomarkers predictive of their risk.
The identification of epigenetic markers of delirium would hopefully lead to improvement in medical and surgical practice.
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Palo Alto,
California
94304
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 198% from $1,137,836 to $3,393,148.
The Leland Stanford Junior University was awarded
Epigenetic Biomarkers Post-Operative Delirium in Elderly Dementia Patients
Project Grant R01AG084710
worth $3,393,148
from National Institute on Aging in September 2024 with work to be completed primarily in Palo Alto California United States.
The grant
has a duration of 4 years 7 months and
was awarded through assistance program 93.866 Aging 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
9/1/24
Start Date
4/30/29
End Date
Funding Split
$3.4M
Federal Obligation
$0.0
Non-Federal Obligation
$3.4M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01AG084710
Transaction History
Modifications to R01AG084710
Additional Detail
Award ID FAIN
R01AG084710
SAI Number
R01AG084710-1768422858
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NN00 NIH National Insitute on Aging
Funding Office
75NN00 NIH National Insitute on Aging
Awardee UEI
HJD6G4D6TJY5
Awardee CAGE
1KN27
Performance District
CA-16
Senators
Dianne Feinstein
Alejandro Padilla
Alejandro Padilla
Modified: 5/21/26