The main objective of the Vascular Subcore is to provide the essential clinical and pathologic resources to study the contribution of cerebrovascular disease to dementia. Several pathogenetic mechanisms have been proposed to explain how vascular disease can lead to cognitive impairment, including: acute infarction, chronic ischemia and compromise of the blood-brain barrier. Various forms of cerebrovascular disease are highly prevalent in elderly persons and are often integral components of AD. These categories of patients, however, have traditionally been excluded from ADRC Clinical Cores. The unique mission of this Subcore is to recruit and follow patients with vascular or mixed dementias.
The specific aims i nclude: 1) recruitment of well-characterized subjects with ischemic vascular dementia, as well as appropriate controls (e.g. subjects with mixed dementia, AD or who are cognitively normal), 2) longitudinal follow-up of subjects, including enrollment in the Rancho Brain Research autopsy program; 3) post-mortem examination of patients including semiquantitative and quantitative characterization of vascular and degenerative lesions in the brain; and 4) distribution of autopsy tissues to ADRC investigators. The resources of this Subcore will support several other research projects, including a comprehensive investigation of neuronal degeneration in the AD visual system. In years 11 to 15, Rancho Los Amigos Medical Center (RLAMC) has been chosen to support these activities for several reasons. Rancho is the site of one of nine State-supported Alzheimer Disease Diagnostic and Treatment Centers (ADDTC) which provides clinical diagnoses and assessment for a variety of dementia patients (120 new patients per year). Approximately 25% of these new patients have mild to moderate dementia and would be appropriate for clinical studies of vascular dementia and vision. An autopsy program has been in smooth operation at Rancho since 1984 (previously, known as the ADRC Cell Quantimetric Core) and will provide neuropathologic data and tissues for research studies.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
5P50AG005142-14
Application #
6234086
Study Section
Project Start
1997-04-15
Project End
1998-03-31
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
14
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Southern California
Department
Type
DUNS #
041544081
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
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
Petok, Jessica R; Myers, Catherine E; Pa, Judy et al. (2018) Impairment of memory generalization in preclinical autosomal dominant Alzheimer's disease mutation carriers. Neurobiol Aging 65:149-157
Cruchaga, Carlos; Del-Aguila, Jorge L; Saef, Benjamin et al. (2018) Polygenic risk score of sporadic late-onset Alzheimer's disease reveals a shared architecture with the familial and early-onset forms. Alzheimers Dement 14:205-214
Davis, Jeremy J (2018) Performance validity in older adults: Observed versus predicted false positive rates in relation to number of tests administered. J Clin Exp Neuropsychol 40:1013-1021
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:
Lin, Ming; Gong, Pinghua; Yang, Tao et al. (2018) Big Data Analytical Approaches to the NACC Dataset: Aiding Preclinical Trial Enrichment. Alzheimer Dis Assoc Disord 32:18-27
Weissberger, Gali H; Nation, Daniel A; Nguyen, Caroline P et al. (2018) Meta-analysis of cognitive ability differences by apolipoprotein e genotype in young humans. Neurosci Biobehav Rev 94:49-58
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
Wang, Junyan; Aydogan, Dogu Baran; Varma, Rohit et al. (2018) Modeling topographic regularity in structural brain connectivity with application to tractogram filtering. Neuroimage 183:87-98

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