There are approximately 1.3 million cases of severe dementia in the United States affecting 5% to 15% of the population age 65 or older. Recent estimates suggest that 20-46% of the population may be affected by age 85. Alzheimer's Disease (AD) accounts for the largest proportion of cases of dementia in persons over the age of 65 years. Of the more common complications of AD, behavioral disturbances such as psychosis and agitation dramatically impact on the quality of life of the patient and caregiver. Psychosis develops in approximately one-third of patients with AD. AD patients who become psychotic often pose a threat to themselves and occasionally to others. Psychotic symptoms often require chronic neuroleptic treatment which may produce neuroleptic sensitivity syndrome and tardive dyskinesia. The management of psychosis and behavioral disturbances in AD often requires intensive care, greater follow-up, and sometimes institutionalization, all of which increase the economic burden of the illness. The ability to predict the development of psychosis or other behavioral disturbances such as agitation would influence the pharmacologic management of AD patients. Because of the many disabling side-effects of neuroleptics, any information delimiting their use would be clinically helpful. If it could be determined early that certain characteristics identify patients who are less likely to develop psychosis, and therefore less likely to require chronic neuroleptic treatment, then, should such patients develop behavioral problems, extra consideration could be given to the use of non-neuroleptic approaches. Also, the economic burden and perhaps the course of the illness could be more realistically estimated for a given patient. Although previous long-term prospective investigations have examined potential risk factors for clinical decline in AD, none has specifically examined risk factors for the development of psychosis or agitation. Because there is evidence from cross-sectional studies that suggests a relationship between EPS, neuropsychological and psychosocial disturbances and psychosis in AD, we considered that these measures, in various combinations, will predict the development and time course of psychosis in AD. The goal of the proposed research is to undertake a five-year prospective study of AD patients in order to identify important motor, neuropsychological, psychosocial and demographic factors related to the risk of developing neurobehavioral disturbances and the time course over which these disturbances develop.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG014291-02
Application #
2517066
Study Section
Mental Disorders of Aging Review Committee (MDA)
Project Start
1996-09-30
Project End
2001-08-31
Budget Start
1997-09-01
Budget End
1998-08-31
Support Year
2
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Psychiatry
Type
Schools of Medicine
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Caligiuri, M P; Peavy, G; Salmon, D P et al. (2003) Neuromotor abnormalities and risk for psychosis in Alzheimer's disease. Neurology 61:954-8
Caligiuri, M P; Peavy, G; Galasko, D R (2001) Extrapyramidal signs and cognitive abilities in Alzheimer's disease. Int J Geriatr Psychiatry 16:907-11
Samuel, W; Caligiuri, M; Galasko, D et al. (2000) Better cognitive and psychopathologic response to donepezil in patients prospectively diagnosed as dementia with Lewy bodies: a preliminary study. Int J Geriatr Psychiatry 15:794-802
Caligiuri, M P; Peavy, G (2000) An instrumental study of the relationship between extrapyramidal signs and psychosis in Alzheimer's disease. J Neuropsychiatry Clin Neurosci 12:34-9
Caligiuri, M P; Rockwell, E; Jeste, D V (1998) Extrapyramidal side effects in patients with Alzheimer's disease treated with low-dose neuroleptic medication. Am J Geriatr Psychiatry 6:75-82