The Alzheimer's Disease Center (ADC) at New York University Langone Medical Center (NYULMC) is an Alzheimer's Disease Core Center (ADCC) that provides outstanding infrastructure, environment and core resources promoting cutting-edge research by bringing together clinical, translational, basic and psychosocial investigators to study the etiology, pathogenesis, diagnosis, treatment and prevention of Alzheimer's disease and related disorders (collectively referred to as AD). Now entering its 25th year, the NYU ADC continues to provide a mechanism for fostering and coordinating the interdisciplinary cooperation of a group of established investigators conducting programs of research on AD while providing a supportive milieu for early-stage investigators. The ADC supports innovative research by maintaining an integrated array of core facilities, including Administrative, Clinical, Neuropathology, Data Management and Statistical, Outreach, Recruitment and Education, and Neuroimaging and Psychosocial Cores. The principal goal of the ADC is to enhance the performance of innovative AD research, including research that may lead to potential disease-modifying therapies. Along with the overall NIA-ADC program, the NYU ADC has moved into a new era, capitalizing on the extraordinary opportunities presented by leveraging the strengths of the network of centers to provide large numbers of samples and standardized clinical, cognitive and biomarker data from well-characterized participants, as well as a large pool of potential participants for future AD-related research. At the same time, we place a strong emphasis on the unique contributions and new directions of the NYU ADC. Additionally, emphasis is placed on possibilities for utilizing the resources within our ADC and across the ADCs to advance and augment drug discovery and drug development for novel therapeutics for AD. Since its inception in 1990, the NYU ADC has facilitated cutting edge research defining normal aging and the transition to the earliest detectable stages of mild cognitive impairment (MCI) and AD. This longstanding research direction will continue to be our main scientific theme, with a particular focus over the past 15 years on better understanding the preclinical stages that precede MCI and mild AD. Thus, we will continue our scientific focus on elucidating the transition from normal aging to the earliest, preclinical stages of AD. Our collective research efforts investigating the clinical-pathological changes associated with cognitive impairment and the role of co-morbid pathologies and chronic conditions position us well to develop, test and validate novel strategies to address symptomatic, disease-modifying, and preventive therapeutic approaches being developed at our ADC and other ADCs.

Public Health Relevance

Now entering its 25th year, the New York University (NYU) Alzheimer's Disease Center (ADC) continues to foster and coordinate interdisciplinary research on Alzheimer's disease (AD) by providing investigators with shared core resources. The principal scientific goal is to enhance the performance of innovative research on the transition from normal aging to very early AD, and to translate this knowledge into the development of disease-modifying therapies that may lead to AD prevention.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
5P30AG008051-28
Application #
9267075
Study Section
Special Emphasis Panel (ZAG1)
Program Officer
Silverberg, Nina B
Project Start
1997-07-15
Project End
2020-04-30
Budget Start
2017-07-01
Budget End
2018-04-30
Support Year
28
Fiscal Year
2017
Total Cost
Indirect Cost
Name
New York University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10010
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:
Kirson, Noam Y; Scott Andrews, J; Desai, Urvi et al. (2018) Patient Characteristics and Outcomes Associated with Receiving an Earlier Versus Later Diagnosis of Probable Alzheimer's Disease. J Alzheimers Dis 61:295-307
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
Adhikari, Bhim M; Jahanshad, Neda; Shukla, Dinesh et al. (2018) Heritability estimates on resting state fMRI data using ENIGMA analysis pipeline. Pac Symp Biocomput 23:307-318
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
Solesio, MarĂ­a E; Peixoto, Pablo M; Debure, Ludovic et al. (2018) Carbonic anhydrase inhibition selectively prevents amyloid ? neurovascular mitochondrial toxicity. Aging Cell :e12787
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
Masurkar, Arjun V (2018) Towards a circuit-level understanding of hippocampal CA1 dysfunction in Alzheimer's disease across anatomical axes. J Alzheimers Dis Parkinsonism 8:
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
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

Showing the most recent 10 out of 604 publications