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The NYU Alzheimer’s Disease Center (ADC) is part of
the Department of Psychiatry at New York University School of Medicine, located
in midtown Manhattan, in New York City, New York. The ADC is one of thirty Alzheimer's
disease research centers in the United States supported by the National Institute
on Aging (NIA). As an NIA-supported research facility, the center's goals are
to advance current knowledge and understanding of brain aging and Alzheimer's
disease, to expand the numbers of scientists working in the field of aging and
Alzheimer's research, to work toward better treatment options and care for those
living with memory impairment, and most importantly, to apply its findings to
the care of patients and their families, and share these findings with healthcare
providers, researchers, and the general public.
The ADC's programs and services are directed toward providing its patients
and their families with the highest quality diagnostic evaluations, the latest
treatment options available, psychosocial support and education that reflect the
most up-to-date information about Alzheimer's disease and memory impairment. The
ADC's programs and services extend to other research facilities and to healthcare
professionals through shared knowledge and collaboration, and to the general public
through seminars, presentations at community centers, the ADC's newsletter and
this web site.
The NYU ADC is made up of seven core facilities that provide
important resources to aging and dementia research programs and scientists at
NYU. Each of these cores has the dual goal of providing quality service to patients
while also furthering the goals of Alzheimer’s research.
The Administrative Core
Clinical Core
Neuropathology Core
Education Core
Data Management and Biostatistics Core
Neuroimaging Core
Psychosocial Core
ADMINISTRATIVE CORE
The Administrative Core of the ADC provides overall administrative
supervision and coordination of the Center to optimize the scientific progress
of affiliated researchers, to ensure an environment conducive to the conduct
of productive research on Alzheimer’s disease and to make certain that
the basic objectives of the ADC are achieved. Annual solicitation and review
of pilot studies to be funded by the ADC is also coordinated by the Administrative
Core.
CLINICAL CORE
The Clinical Core provides well-diagnosed research participants for scientists
conducting clinical studies therefore provides participants with expert, accurate
diagnostic cognitive evaluations and maintains the information and clinical material
from these evaluations for further study. Participants are followed over time
from first diagnosis to post mortem examination, for those enrolled in the brain
donation program. The Core ensures that participants are matched with clinical
research projects that are appropriate for them.
NEUROPATHOLOGY CORE
The Neuropathology Core is best known to research participants
and their families for its brain donation program. Through the brain donation
program and other efforts, this core conducts thorough postmortem examinations
(autopsies) and maintains a brain bank for continued study by Alzheimer’s
researchers.
The studies conducted by this Core, either independently
or through collaboration with other research facilities, provide information
valuable to understanding the progression of Alzheimer’s disease, from
its earliest onset to its latest stages, and to contribute to discovering the
causes of this disease.
EDUCATION CORE
Most ADC research participants learn about the Alzheimer’s
Disease Center through the outreach efforts of this Core. The Education Core
provides the general public with information through seminars, education meetings,
memory screenings, newsletters and this web site.
The goals of this Core are to:
- educate the elderly and their family members about normal aging and dementia
- educate caregivers, providing them with up-to-date information
available at research institutions about diagnosis and management of Alzheimer’s
disease.
- educate health care professionals -
physicians, nurses and social workers - and students entering these professions
about state-of-the-art methods for accurate diagnosis of MCI and AD, the importance
of participating in clinical trials, and best practices for caring for a person
with MCI and AD and helping their family members.
- educate support and resource providers in the community
about normal cognitive change to be expected with aging, recognition of early
signs of dementia in the elderly and the benefits of early diagnosis, treatment
and appropriate referral.
In addition to working with the general public and health and service providers,
this Core also works to expand the number of scientists trained to conduct AD
research and facilitate transfer of information among research specialties in
AD.
THE DATA MANAGEMENT AND STATISTICS CORE (DATA CORE)
The Data Core performs data management and analysis for all the Cores of the ADC and for individual research projects. The Core maintains all data in a centralized database, and offers consultation in statistical analysis. The centralization of these functions makes it possible for each of the research projects to benefit from more sophisticated and flexible statistical and computer tools than would normally be available for any single project and fosters sharing of data among collaborating investigators in the ADC.
NEUROIMAGING CORE
The MRI and PET scan studies for participants of the ADC undergoing a comprehensive
memory evaluation are provided and interpreted under the mandate of the Neuroimaging
core. This data together with other research efforts contribute to the understanding
of the markers that signify the progression of the illness. This data is categorized
and organized in a user friendly format that facilitates its use by the other
cores and by collaborating researchers.
PSYCHOSOCIAL CORE
The Psychosocial Core provides counseling, support and resource
information to patients and families at the NYU-ADC. This Core contributes to
Alzheimer’s
research by studying the relationship between psychosocial data on individuals
with MCI, AD, and their family members and clinical data collected during the
Clinical Core evaluation of ADC subjects. The Psychosocial Core makes possible
the development of new treatment and care strategies, and investigation of the
impact of living with Alzheimer’s disease and other related disorders either
as the person with the illness or as a caregiving partner.
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