R01AG054070
Project Grant
Overview
Grant Description
Offspring Study of Mechanisms for Racial Disparities in Alzheimer's Disease - Project Summary
The overall aim of this study is to identify social and biological pathways of racial/ethnic disparities for incident mild cognitive impairment (MCI)/Alzheimer's disease and related disorders (ADRD) and cognitive decline that emerge in middle age.
We have recruited over 1,500 middle-aged offspring of participants in the Washington Heights/Inwood Columbia Aging Project (WHICAP), and characterized them at baseline using measures of neuropsychological and psychosocial function, lifecourse measures of social and environmental determinants of health, stored blood samples, and brain structure with MRI.
The offspring study is unique among other cohorts, with large numbers of Latinx and African American participants in middle age who are not a convenience sample and are representative of their age and cultural groups, and whose parents are well-characterized with directly observed clinical and biological data.
Our prior work in the offspring cohort found 1) lower memory and executive function among middle-aged people whose parents have MCI/AD, particularly among non-Latinx whites compared with non-Latinx blacks and Latinx, 2) among whites, parental cognition had a stronger impact on offspring hippocampal volume, and among blacks, parental cognition had a stronger impact on offspring WMH, 3) the negative impact of age on cognitive function and cortical thickness is disproportionately large among black and Latinx participants compared with whites, 4) early life social factors such as parental SES promote cognitive resilience to parental AD history, and 5) racial discrimination has a disproportionate negative impact on cognitive test performance among black and Spanish-speaking Latinx offspring relative to white offspring.
Over the next 5 years, we propose to recruit additional offspring for a total sample of 2,500, obtain baseline MRI scans on an additional 1,000 participants, obtain plasma biomarkers for AD risk and neurodegeneration on baseline blood samples, and obtain two repeat assessments of cognitive, psychosocial, and medical function.
Our overarching hypothesis is that vascular and inflammatory pathways of transmission of parental AD risk play a greater role among black and Latinx older adults compared with whites, and that socioeconomic status, educational quality, and experience of discrimination will moderate the relationship between parental AD status and biomarkers of AD on offspring cognition.
Specifically, the project will 1) examine the impact of biological markers of vascular and inflammatory health, AD pathophysiology, neurodegeneration, biological aging, and genetic risk on cognitive decline and incident impairment across race/ethnicity and sex/gender, and 2) determine the lifecourse educational, economic, and social moderators of parental AD risk and AD biomarkers on cognitive decline and incident impairment across race/ethnicity and sex/gender.
The overall aim of this study is to identify social and biological pathways of racial/ethnic disparities for incident mild cognitive impairment (MCI)/Alzheimer's disease and related disorders (ADRD) and cognitive decline that emerge in middle age.
We have recruited over 1,500 middle-aged offspring of participants in the Washington Heights/Inwood Columbia Aging Project (WHICAP), and characterized them at baseline using measures of neuropsychological and psychosocial function, lifecourse measures of social and environmental determinants of health, stored blood samples, and brain structure with MRI.
The offspring study is unique among other cohorts, with large numbers of Latinx and African American participants in middle age who are not a convenience sample and are representative of their age and cultural groups, and whose parents are well-characterized with directly observed clinical and biological data.
Our prior work in the offspring cohort found 1) lower memory and executive function among middle-aged people whose parents have MCI/AD, particularly among non-Latinx whites compared with non-Latinx blacks and Latinx, 2) among whites, parental cognition had a stronger impact on offspring hippocampal volume, and among blacks, parental cognition had a stronger impact on offspring WMH, 3) the negative impact of age on cognitive function and cortical thickness is disproportionately large among black and Latinx participants compared with whites, 4) early life social factors such as parental SES promote cognitive resilience to parental AD history, and 5) racial discrimination has a disproportionate negative impact on cognitive test performance among black and Spanish-speaking Latinx offspring relative to white offspring.
Over the next 5 years, we propose to recruit additional offspring for a total sample of 2,500, obtain baseline MRI scans on an additional 1,000 participants, obtain plasma biomarkers for AD risk and neurodegeneration on baseline blood samples, and obtain two repeat assessments of cognitive, psychosocial, and medical function.
Our overarching hypothesis is that vascular and inflammatory pathways of transmission of parental AD risk play a greater role among black and Latinx older adults compared with whites, and that socioeconomic status, educational quality, and experience of discrimination will moderate the relationship between parental AD status and biomarkers of AD on offspring cognition.
Specifically, the project will 1) examine the impact of biological markers of vascular and inflammatory health, AD pathophysiology, neurodegeneration, biological aging, and genetic risk on cognitive decline and incident impairment across race/ethnicity and sex/gender, and 2) determine the lifecourse educational, economic, and social moderators of parental AD risk and AD biomarkers on cognitive decline and incident impairment across race/ethnicity and sex/gender.
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
New York,
New York
100323720
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 304% from $3,429,627 to $13,839,964.
The Trustees Of Columbia University In The City Of New York was awarded
Racial Disparities in Alzheimer's Disease Study
Project Grant R01AG054070
worth $13,839,964
from National Institute on Aging in September 2016 with work to be completed primarily in New York New York United States.
The grant
has a duration of 9 years 8 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 6/5/24
Period of Performance
9/1/16
Start Date
5/31/26
End Date
Funding Split
$13.8M
Federal Obligation
$0.0
Non-Federal Obligation
$13.8M
Total Obligated
Activity Timeline
Transaction History
Modifications to R01AG054070
Additional Detail
Award ID FAIN
R01AG054070
SAI Number
R01AG054070-2734126211
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Private Institution Of Higher Education
Awarding Office
75NN00 NIH NATIONAL INSITUTE ON AGING
Funding Office
75NN00 NIH NATIONAL INSITUTE ON AGING
Awardee UEI
QHF5ZZ114M72
Awardee CAGE
3FHD3
Performance District
NY-13
Senators
Kirsten Gillibrand
Charles Schumer
Charles Schumer
Budget Funding
Federal Account | Budget Subfunction | Object Class | Total | Percentage |
---|---|---|---|---|
National Institute on Aging, National Institutes of Health, Health and Human Services (075-0843) | Health research and training | Grants, subsidies, and contributions (41.0) | $7,035,618 | 100% |
Modified: 6/5/24