This application proposes the addition of a Neuroimaging Core (NIC) to the newly established Alzheimer?s Disease Core Center (ADCC) at Wake Forest School of Medicine. The NIC will address a critical need to establish biomarkers that reliably differentiate Alzheimer?s disease (AD) from other conditions that affect cognition in aging. Recently, an AD research framework was developed for a biologically-based classification to enhance identification of disease mechanisms, to appropriately target therapeutic interventions, and to track therapeutic response and disease progression. Neuroimaging techniques, such as magnetic resonance imaging (MRI) to measure structural changes and positron emission tomography (PET) to track changes in pathological hallmarks such as b-amyloid and tau, comprise a powerful approach to characterize the progressive pathology associated with cognitive decline and to differentiate AD from other dementias. To establish reliable biomarkers associated with AD and other conditions that impair cognition with aging will require a large collaborative effort and the national NIH ADC network is ideally suited to address this need. The Wake Forest ADCC can make unique contributions to the network; the NIC will conduct longitudinal, multimodal neuroimaging paired with phenotypic and genomic characterization of a diverse cohort of participants. The NIC will provide expertise and resources to complement the ADCC themes, which focus on: 1) early transitions from normal aging to mild cognitive impairment (MCI) and AD; 2) the role of metabolic and vascular risk in these transitions; and 3) ethnic differences modulating these relationships.
The first aim of the NIC will be to leverage existing Clinical Core and imaging infrastructure, including research-dedicated PET and MRI, cyclotron, and advanced analytic pipelines to help identify the causes of AD and develop novel strategies for prevention and treatment. As a second aim, the NIC will optimize participation of underrepresented groups in neuroimaging protocols, with a special focus on African-Americans, to better understand and reduce disparities in their risk of AD and other dementias.
The third aim will be to expand interactions with the ADC network and NACC, and with institutional partners through aligned neuroimaging methods and new collaborations.
The final aim will be to provide training and consultation on the latest scientific advances in neuroimaging to ADCC-affiliated investigators. Through these aims, the Wake Forest ADCC NIC will further the understanding of AD pathology and its relationship to cognitive decline and will significantly enhance the Center?s contribution to the ADC network and to investigators worldwide.

Public Health Relevance

This application proposes the addition of a new Neuroimaging Core to the Wake Forest Alzheimer?s Disease Core Center (ADCC). Establishment of this Neuroimaging Core will enable long-term, repeated observation of the pathological changes associated with cognitive decline in Alzheimer?s disease using multiple neuroimaging techniques in well-characterized study participants. The Neuroimaging Core will help Wake Forest ADCC researchers differentiate AD from other dementias and address important scientific questions, such as the contributions of vascular and metabolic risk factors in multiple ethnic groups, and will greatly expand the resources that are provided by the ADCC to the broader Alzheimer?s disease research field. !

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
3P30AG049638-04S1
Application #
9705333
Study Section
Special Emphasis Panel (ZAG1)
Program Officer
Silverberg, Nina B
Project Start
2016-09-01
Project End
2021-06-30
Budget Start
2019-08-01
Budget End
2020-06-30
Support Year
4
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Wake Forest University Health Sciences
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
937727907
City
Winston-Salem
State
NC
Country
United States
Zip Code
27157
Crum, Jana; Wilson, Jeffrey; Sabbagh, Marwan (2018) Does taking statins affect the pathological burden in autopsy-confirmed Alzheimer's dementia? Alzheimers Res Ther 10:104
Kamara, Dennis M; Gangishetti, Umesh; Gearing, Marla et al. (2018) Cerebral Amyloid Angiopathy: Similarity in African-Americans and Caucasians with Alzheimer's Disease. J Alzheimers Dis 62:1815-1826
Kaur, Antarpreet; Edland, Steven D; Peavy, Guerry M (2018) The MoCA-Memory Index Score: An Efficient Alternative to Paragraph Recall for the Detection of Amnestic Mild Cognitive Impairment. Alzheimer Dis Assoc Disord 32:120-124
Brenowitz, Willa D; Han, Fang; Kukull, Walter A et al. (2018) Treated hypothyroidism is associated with cerebrovascular disease but not Alzheimer's disease pathology in older adults. Neurobiol Aging 62:64-71
Gallagher, Damien; Kiss, Alex; Lanctot, Krista L et al. (2018) Toward Prevention of Mild Cognitive Impairment in Older Adults With Depression: An Observational Study of Potentially Modifiable Risk Factors. J Clin Psychiatry 80:
Espeland, Mark A; Carmichael, Owen; Yasar, Sevil et al. (2018) Sex-related differences in the prevalence of cognitive impairment among overweight and obese adults with type 2 diabetes. Alzheimers Dement 14:1184-1192
Barnes, Josephine; Bartlett, Jonathan W; Wolk, David A et al. (2018) Disease Course Varies According to Age and Symptom Length in Alzheimer's Disease. J Alzheimers Dis 64:631-642
Gallagher, Damien; Kiss, Alex; Lanctot, Krista et al. (2018) Depression and Risk of Alzheimer Dementia: A Longitudinal Analysis to Determine Predictors of Increased Risk among Older Adults with Depression. Am J Geriatr Psychiatry 26:819-827
Haaksma, Miriam L; Calderón-Larrañaga, Amaia; Olde Rikkert, Marcel G M et al. (2018) Cognitive and functional progression in Alzheimer disease: A prediction model of latent classes. Int J Geriatr Psychiatry 33:1057-1064
Ramsey, Christine M; Gnjidic, Danijela; Agogo, George O et al. (2018) Longitudinal patterns of potentially inappropriate medication use following incident dementia diagnosis. Alzheimers Dement (N Y) 4:1-10

Showing the most recent 10 out of 34 publications