Project Grant R01AG083423
- This Project Grant award of $4,787,820.00 from the National Institute on Aging (CFDA 93.866 - Aging Research) aims to gain a better understanding of the individual- and system-level characteristics that influence diagnosis of mild cognitive impairment (MCI) and Alzheimer's disease and related dementias (ADRD), and how diagnosis can moderate the effects of cognitive decline on employment, future care, and quality of life. The key objectives are to: 1) examine whether older adults experiencing...
- The National Institute on Aging (NIA) awarded a $3,281,385 Project Grant under the Aging Research federal grant program (CFDA 93.866) to the University of California, San Diego (UCSD) to leverage 30 years of Alzheimer's disease clinical trials data. The goal is to examine the role of specific patient phenotypes, such as sex/gender, APOE4 status, and polygenic hazard scores, on response to drug or lifestyle interventions. The project will analyze data from 14,602 participants across multiple...
- This Project Grant award of $353,391.00, provided by the National Institute on Aging (CFDA 93.866 - Aging Research), aims to validate the use of a "Personal Learning Curve" paradigm as a sensitive marker of early memory decline related to Alzheimer's disease (AD) biomarkers in a large, diverse sample of older adults. The study seeks to determine if this digital cognitive assessment tool, which measures learning over repeated evaluations, can detect subtle AD-related memory failures...
- This Project Grant award from the National Institute on Aging (CFDA 93.866 - Aging Research) for $791,086 aims to develop computational models that can predict the presence of non-Alzheimer's disease neuropathological changes, such as Lewy body disease, TDP-43 proteinopathy, and cerebral amyloid angiopathy, in individuals with Alzheimer's disease neuropathological changes. The project will leverage data from autopsy-confirmed datasets, in vivo neuroimaging, and clinical assessments to build...
- This Project Grant award from the National Institute on Aging (CFDA 93.866 Aging Research) in the amount of $297,000.00 will support a mixed methods study to understand the challenges and benefits of delivering new Alzheimer's disease (AD) drugs equitably to African American and white patients in Alabama. The objective is to assess access to care barriers, perceived value, and costs and benefits of new AD drugs for these two populations. In the initial R61 planning phase, the University of...
- This federal Project Grant award of $372,690, provided by the National Institute on Aging (CFDA 93.866 Aging Research), aims to comprehensively understand the heterogeneous causal pathophysiology of Alzheimer's disease (AD). The key objectives are to: (1) develop new statistical methods for uncovering heterogeneous causal relationships among amyloid-beta, tau accumulation, and cognition across diverse AD datasets; (2) apply these methods to reveal optimal treatment windows and target populations...
- This $1,012,879 Project Grant was awarded by the National Institute on Aging (CFDA 93.866 - Aging Research) to New York University (NYU) to develop three novel statistical machine learning methods for Alzheimer's disease (AD) research using multi-view imaging, genomic, and clinical data. The specific aims include: 1) developing a multi-view data decomposition method to construct brain and genomic networks across AD statuses, 2) developing an optimal false discovery rate control method to...
- This Project Grant award from the National Institutes of Health (NIH) Office of the Director under the Trans-NIH Research Support program (CFDA 93.310) provides $322,000.00 to Case Western Reserve University to perform the following: Analyze electroencephalographic (EEG) and plasma Alzheimer's disease (AD) biomarker data collected during a previous clinical trial studying the effects of the drug memantine on adolescents and young adults with Down syndrome. The analysis will examine the...
- The National Institute on Aging (NIA), under the Aging Research Federal Grant Program (CFDA 93.866), awarded a $129,330 Project Grant to The General Hospital Corporation, doing business as Massachusetts General Hospital (MGH), to conduct research on profiling and forecasting individual progression in Alzheimer's disease and related dementias (ADRD). The key objectives of this 5-year project are to: 1) deploy a multi-modal information framework that leverages decades-long in vivo and digital...
- This federal Project Grant award of $307,000.00 from the National Institute on Aging (CFDA 93.866 - Aging Research) aims to conduct a single, highly powered study to identify memory processes that are most sensitive to the asymptomatic, preclinical stage of Alzheimer's disease (AD) pathology. The study combines a continuous report item-location associative memory task with advanced behavioral and neural modeling to estimate subtle changes in memory precision that may differentiate healthy...
STATISTICAL METHODS TO CHARACTERIZE PATIENTS WHO HIGHLY BENEFIT ACROSS MULTIFACETED CLINICAL OUTCOMES, FROM TREATMENTS IN ALZHEIMERS DISEASE AND RELATED DEMENTIAS (ADRD) - PROJECT SUMMARY METHODS TO CHARACTERIZE PATIENTS WHO HIGHLY BENEFIT ON MULTIPLE CLINICAL OUTCOMES, FROM TREATMENTS IN ALZHEIMER'S DISEASE AND RELATED DEMENTIAS (ADRD), ARE NECESSARY TO TREAT PATIENTS EFFECTIVELY. TREATMENTS MAY BENEFIT SOME PATIENTS ON TARGETED OUTCOMES, BUT HARM SOME PATIENTS ON OTHER, E.G., COGNITIVE, OUTCOMES. SO, CHARACTERIZING PATIENTS WHO HIGHLY BENEFIT ON MULTIPLE OUTCOMES IS SIGNIFICANT: FIRST IT ALLOWS THESE PATIENTS TO CHOOSE A TREATMENT IF IT IS PREDICTED TO GIVE THEM HIGH BENEFITS WITHOUT THE HARMS; SECOND, ACCURATE CHARACTERIZATION METHODS DO NOT EXIST. GENERALLY, A CHARACTERIZATION METHOD HAS TWO STAGES. ONE STAGE "CONSTRUCTS" OUTCOME PREDICTIONS BASED ON PATIENTS' COVARIATES; AND ANOTHER STAGE "SYNTHESIZES" THE PREDICTIONS TO ESTIMATE THE GOAL - A LARGE HIGH BENEFIT GROUP. AS THE "CONSTRUCTION" STAGE USES MANY COVARIATES, IT NEEDS METHODS TO ESTIMATE PREDICTIONS FROM A MODEL, I.E., FROM A LARGE SET OF POSSIBLE DISTRIBUTIONS (E.G., REGRESSION, NEURAL NETWORKS). THESE PREDICTIONS ARE THEN USED IN THE "SYNTHESIS" STAGE FOR THE GOAL. SUCH EXISTING METHODS, HOWEVER, DO NOT USE THE CLINICAL GOAL (TO CHARACTERIZE HIGH-BENEFIT PATIENTS) AS A GUIDE INSIDE THE CONSTRUCTION STAGE. FOR A SINGLE OUTCOME, RECENT WORK HAS SHOWN THAT THIS LACK OF LINKING CAN PRODUCE DRAMATICALLY INACCURATE CHARACTERIZATIONS, NO MATTER THE MODEL. FOR CHARACTERIZING PATIENTS WITH MULTIPLE HIGH BENEFITS, NEW METHODS MUST EXPLICITLY LINK ALL MULTIPLE CLINICAL GOALS (I.E. HIGH BENEFITS IN ALL OUTCOMES) IN THE CONSTRUCTION STAGE. IN PREPARATORY WORK, WE SHOWED THAT EXISTING METHODS FOR MULTIPLE OUTCOMES, CAN MISS EVEN MOST OF THE HIGH BENEFIT PATIENTS, AND WE DEVELOPED A PRELIMINARY BETTER METHOD BY ESTABLISHING THE MISSING LINKS. THIS NEW PROJECT IS MOTIVATED BY OUR ONGOING WORK WITH TWO STUDIES. THE FIRST STUDY TESTED IF CITALOPRAM REDUCES AGITATION IN ALZHEIMER'S PATIENTS. SINCE CITALOPRAM MAY HARM COGNITIVE FUNCTION, WE SET TO CHARACTERIZE PATIENTS WITH HIGH CITALOPRAM EFFECT IN (A) REDUCING AGITATION AND (B) MAINTAINING COGNITIVE FUNCTION. THE SECOND STUDY TESTS THE EFFECT OF TRANSCRANIAL DIRECT CURRENT STIMULATION ON PRIMARY PROGRESSIVE APHASIA OUTCOMES, WITH RELATED GOALS. IN PREPARATORY WORK, WE FOUND STRONG EVIDENCE THAT STANDARD METHODS MISS UP TO 70% OF THE PATIENTS WITH MULTIPLE HIGH BENEFITS, COMPARED TO THE NEW METHODS. FOR THIS PROJECT WE PROPOSE TO FULLY DEVELOP METHODS TO CHARACTERIZE PATIENTS WHO HIGHLY BENEFIT ON MULTIPLE OUTCOMES. THE METHODS WILL BE APPLIED TO THE ABOVE STUDIES, AND CAN HELP MORE GENERALLY IN OTHER ADRD STUDIES. AIM 1. DEVELOP METHODS TO CHARACTERIZE PATIENTS WHO HIGHLY-BENEFIT IN MULTIPLE OUTCOMES IN RANDOMIZED TRIALS. THESE METHODS ARE SIGNIFICANT BECAUSE THEY ALLOW ACCURATE PERSONALIZED TREATMENT CHOICES. AIM 2. DEVELOP METHODS TO FIND IF A SIMPLER SUBSET OF THE FULL MULTIPLE OUTCOMES, CAN HAVE SIMILAR PATIENT CHARACTERIZATION AS THE FULL OUTCOMES. THESE METHODS ARE SIGNIFICANT BECAUSE THEY CAN SUGGEST IF A HIGH-EFFECT ON EARLIER OUTCOMES IS NECESSARY BEFORE A HIGH-EFFECT ON THE LATER OUTCOMES OCCURS. AIM 3. DEVELOP METHODS TO CHARACTERIZE PATIENTS WHO HIGHLY BENEFIT IN MULTIPLE OUTCOMES IN OBSERVATIONAL STUDIES. THESE METHODS ARE SIGNIFICANT WHEN RANDOMIZATION IS INFEASIBLE.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $35.2k | 8/14/25 | ||
| Not listed | $396.2k | 1/16/25 | ||
| Not listed | $396.2k | 1/16/25 | ||
| Not listed | $471.9k | 4/23/24 | ||
| Not listed | $471.9k | 4/23/24 |
GrantNumber | Description | Subgrantee | Prime Award | Dollars Obligated | Updated At |
|---|---|---|---|---|---|
2006415094S | Temple University-Of The Commonwealth System Of Higher Education | Project Grant R01AG083423 | $164.7k | 5/1/25 | |
2006438415S | The Leland Stanford Junior University | Project Grant R01AG083423 | $305.6k | 3/14/25 |