The purpose of this application is to establish an Imaging Core for the Northwestern Alzheimer?s Disease Center (ADC) to enhance research activities on aging and dementia within and outside of Northwestern University.
The Aims of this proposal are to: 1) Initiate a Imaging Core in our current cycle focusing on the spectrum from healthy cognitive aging to dementia, including the FTLD-spectrum of disorders using imaging modalities that will yield optimal quantitative information on brain structure (MP-RAGE), white matter integrity (FLAIR), axonal pathways (dMRI), resting state hemodynamic fluctuations for establishing functional connectivity (rs-fMRI), blood flow (ASL) as well as amyloid and tau binding (amyloid-PET, tau-PET). 2) Establish a secure database, automated pipelines for processing imaging files, and tools for exploring and accessing the data to facilitate data analysis in order to leverage projects of our collaborators and to contribute to multi-center data repositories such as the National Alzheimer?s Coordinating Center (NACC). 3) Integrate imaging parameters with clinical and post-mortem information on Clinical Core subjects in a unified database so that control subjects can be more fully characterized, patient groups have more solid diagnostic information and clinico- pathologic correlations can be guided by pre-mortem imaging biomarkers. Nearly all aspects of the Northwestern ADC will be enhanced by the availability of the Imaging Core. For example, the diagnostic, anatomical and physiological characterization of Clinical Core subjects who participate in collaborative studies will be improved and all clinical investigations at the Northwestern ADC will be able to access more sophisticated tools for correlating imaging markers with behavioral and clinical parameters. The Imaging Core will unburden researchers using Clinical Core subjects from the need to gather ad hoc imaging data and will add a new dimension to clinicopathologic investigations of autopsy specimens. Thus, the range of hypotheses that can be addressed by collaborative projects relying on Northwestern ADC resources will be increased. An additional and consequential benefit will be to create new training and research opportunities for young investigators and clinicians at the Northwestern ADC. The imaging data generated by this proposal will also improve the amount of available multimodal data available in NACC, which will benefit extramural research.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
3P30AG013854-23S2
Application #
9358004
Study Section
Special Emphasis Panel (ZAG1)
Project Start
Project End
Budget Start
2017-07-01
Budget End
2018-06-30
Support Year
23
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Northwestern University at Chicago
Department
Type
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
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
Bergeron, David; Gorno-Tempini, Maria L; Rabinovici, Gil D et al. (2018) Prevalence of amyloid-? pathology in distinct variants of primary progressive aphasia. Ann Neurol 84:729-740
Kim, Garam; Bolbolan, Kabriya; Gefen, Tamar et al. (2018) Atrophy and microglial distribution in primary progressive aphasia with transactive response DNA-binding protein-43 kDa. Ann Neurol 83:1096-1104
Pottier, Cyril; Zhou, Xiaolai; Perkerson 3rd, Ralph B et al. (2018) Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. Lancet Neurol 17:548-558
Gefen, Tamar; Papastefan, Steven T; Rezvanian, Aras et al. (2018) Von Economo neurons of the anterior cingulate across the lifespan and in Alzheimer's disease. Cortex 99:69-77
Kim, Garam; Vahedi, Shahrooz; Gefen, Tamar et al. (2018) Asymmetric TDP pathology in primary progressive aphasia with right hemisphere language dominance. Neurology 90:e396-e403
Burke, Shanna L; Maramaldi, Peter; Cadet, Tamara et al. (2018) Decreasing hazards of Alzheimer's disease with the use of antidepressants: mitigating the risk of depression and apolipoprotein E. Int J Geriatr Psychiatry 33:200-211
Weintraub, Sandra; Besser, Lilah; Dodge, Hiroko H et al. (2018) Version 3 of the Alzheimer Disease Centers' Neuropsychological Test Battery in the Uniform Data Set (UDS). Alzheimer Dis Assoc Disord 32:10-17
Qian, Winnie; Fischer, Corinne E; Schweizer, Tom A et al. (2018) Association Between Psychosis Phenotype and APOE Genotype on the Clinical Profiles of Alzheimer's Disease. Curr Alzheimer Res 15:187-194
Wilmoth, Kristin; LoBue, Christian; Clem, Matthew A et al. (2018) Consistency of traumatic brain injury reporting in older adults with and without cognitive impairment. Clin Neuropsychol 32:524-529

Showing the most recent 10 out of 443 publications