The Genetics Coordinating Core (GCC) at Columbia has been in existence for two years. The Core was initially supported through a supplement from the National Institute on Aging (NIA), Alzheimer's Disease Research Centers (ADRC/ADC) Program, with the goal of coordinating the collection of families in which two or more individuals have Alzheimer's disease from the collaborating centers. The overall program is entitled the NIA-Genetics Initiative for Late-Onset Alzheimer's Disease (NIA-LOAD Study). The collection of these families was designed using a multi-center approach that originally included 10 ADCs and was later expanded to include 18 centers for which Columbia University's ADRC has been the Coordinating Center. In addition, ADCs not included in the NIA Genetics Initiative have been able to submit families for consideration. Over the past year and a half, the GCC at the Columbia ADRC has developed, circulated and refined a procedures manual, reviewed and approved over 500 families for inclusion in the National Cell Repository for Alzheimer's Disease (NCRAD), specified the type of data to be collected and transmitted to NCRAD and have developed standardized format to collect age-at-onset, assess cognitive performance, collect biomarkers and autopsy material. The goals for the GCC over the next 5 years are to: expand the current collection of families by identifying and examining new families meeting NIA-LOAD criteria for inclusion, assist the participating centers to identify newly affected family members within existing families, develop and implement follow-up procedures, including autopsy, for the participating families and family members, facilitate and coordinate the recruitment of up to 1,000 individuals unrelated to the participating families without dementia to form """"""""control"""""""" group similar in age, sex and ethnic background for association analyses by using similar methods to identify potential individuals, and develop and implement methods for standardized assessment of a series of quantitative traits for application in the NIA-LOAD study.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
5P50AG008702-19
Application #
7628489
Study Section
Special Emphasis Panel (ZAG1)
Project Start
Project End
Budget Start
2008-06-01
Budget End
2009-05-31
Support Year
19
Fiscal Year
2008
Total Cost
$375,156
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Guerreiro, Rita; Ross, Owen A; Kun-Rodrigues, Celia et al. (2018) Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study. Lancet Neurol 17:64-74
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
Miranda, André M; Lasiecka, Zofia M; Xu, Yimeng et al. (2018) Neuronal lysosomal dysfunction releases exosomes harboring APP C-terminal fragments and unique lipid signatures. Nat Commun 9:291
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
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
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
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
Ting, Simon Kang Seng; Foo, Heidi; Chia, Pei Shi et al. (2018) Dyslexic Characteristics of Chinese-Speaking Semantic Variant of Primary Progressive Aphasia. J Neuropsychiatry Clin Neurosci 30:31-37
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:
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

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