This application reflects the continuing commitment of Stanford University to the study of Alzheimer's Disease (AD). Since the inception of the National Institute of Mental Health (NIMH) program for the Study of Psychopathology in the Elderly over 13 years ago, we have had an NIMH Center focusing on the study of AD. Similar to the AIA """"""""Alzheimer's Disease Core Center (ADCC),"""""""" the structure of our NIMH Center focusing on the study of AD. Similar to the NIA """"""""Alzheimer's Disease Core Centers (ADCC), the structure of NIMH Center has been that of an """"""""enabling or core center"""""""" designed to use """"""""core resources"""""""" to facilitate the development of independently funded research on AD. We feel that we been successful in this endeavor, producing funded AD projects at Stanford using the Center's core. Our plan for the future is to continue along this track as an ADCC because the objectives and structure of our Center our Center are more consistent with the mandate of the NIA program than with new NIMH programs that will no long support """"""""core centers"""""""" Given our log history as an enabling center with established cores, we feel that we are ideally suited to accomplish this transition. The primary focus of our Center has been the study of aspects for the heterogeneity of AD. In the current application we have expanded the focus of our proposed ADCC to facilitate research in three major areas: etiology; progression of disease; and pathophysiology of associated behavioral symptoms in AD. This work will be closely integrated with major research programs at the University in basic neurosciences and genetics, neuroimaging, and sleep/chronobiology. Our expectation is that we will not only facilitate research in these three individual areas but also, because of our interdisciplinary experience, we will foster research efforts that bridge disciplines and increase cross-fertilization of ideas. We feel that this multi-factorial and interdisciplinary approach may best address complex questions current to AD research.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
1P30AG017824-01
Application #
6080792
Study Section
Special Emphasis Panel (ZAG1-PCR-5 (J1))
Program Officer
Phelps, Creighton H
Project Start
2000-09-01
Project End
2005-04-30
Budget Start
2000-09-01
Budget End
2001-04-30
Support Year
1
Fiscal Year
2000
Total Cost
$538,217
Indirect Cost
Name
Stanford University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Kawai, Makoto; Beaudreau, Sherry A; Gould, Christine E et al. (2016) Delta Activity at Sleep Onset and Cognitive Performance in Community-Dwelling Older Adults. Sleep 39:907-14
Garrett, A; Gupta, S; Reiss, A L et al. (2015) Impact of 5-HTTLPR on hippocampal subregional activation in older adults. Transl Psychiatry 5:e639
Tinklenberg, Jared R; Kraemer, Helena C; Yaffe, Kristine et al. (2015) Donepezil treatment in ethnically diverse patients with Alzheimer disease. Am J Geriatr Psychiatry 23:384-90
Adamson, Maheen M; Taylor, Joy L; Heraldez, Daniel et al. (2014) Higher landing accuracy in expert pilots is associated with lower activity in the caudate nucleus. PLoS One 9:e112607
Waring, Jill D; Etkin, Amit; Hallmayer, Joachim F et al. (2014) Connectivity underlying emotion conflict regulation in older adults with 5-HTTLPR short allele: a preliminary investigation. Am J Geriatr Psychiatry 22:946-50
Schröder, Carmen M; Primeau, Michelle M; Hallmayer, Joachim F et al. (2014) Serotonin transporter polymorphism is associated with increased apnea-hypopnea index in older adults. Int J Geriatr Psychiatry 29:227-35
OýýHara, Ruth; Marcus, Peter; Thompson, Wesley K et al. (2012) 5-HTTLPR short allele, resilience, and successful aging in older adults. Am J Geriatr Psychiatry 20:452-6
Davies, Helen D; Sridhar, Sneha B; Newkirk, Lori A et al. (2012) Gender differences in sexual behaviors of AD patients and their relationship to spousal caregiver well-being. Aging Ment Health 16:89-101
Thompson, Wesley K; Hallmayer, Joachim; O'Hara, Ruth et al. (2011) Design considerations for characterizing psychiatric trajectories across the lifespan: application to effects of APOE-?4 on cerebral cortical thickness in Alzheimer's disease. Am J Psychiatry 168:894-903
Adamson, Maheen M; Hutchinson, J Benjamin; Shelton, Amy L et al. (2011) Reduced hippocampal activity during encoding in cognitively normal adults carrying the APOE ?4 allele. Neuropsychologia 49:2448-55

Showing the most recent 10 out of 63 publications