Dementia and depression are common problems in geriatric patients and account for many nursing home admissions each year. Mental function loss in the earliest stages of Alzheimer's dementia is often complicated by depression, creating a diagnostic dilemma that hampers treatment and effective coping strategies. Sleep and certain EEG measures are altered in Alzheimer's dementia, perhaps due to degeneration in cholinergic brain pathways. Our initial studies among non-depressed elderly revealed that sleep and EEG variables serve well as markers for early Alzheimer's dementia. This project seeks to confirm and expand these studies, examining these and other potential diagnostic markers in medically healthy communtiy elderly, with and without diagnosable mild Alzheimer's dementia. Sleep and EEG (frequency, power and coherence) measures will be evaluated for two desirable qualities: (1) ability to discriminate mild dementia from non-dementia and (2) ability to discriminate mild dementia from major depression. A major depression subject group will be studied in order to identify and eliminate all measures that are affected in the same way by both depression and dementia. Ability to discriminate mild dementia from non-dementia (or from major depression) will be evaluated using a series of discriminant analyses (DA). Predictor variables emerging in these DAs will be reexamined using previous subject groups in order to replicate results wherever possible. Sensitivity and specificity of the best predictor variables will be calculated. It is possible that useful diagnostic markers for the earliest stages of Alzheimer's dementia may result. A second objective is to further evaluate these predicator variables as correlates of cognitive loss using multiple regression analyses. A series of cognitive tests, covering both dementia and nondementia ranges of cognition will be examined. We hypothesize that primary neuronal degeneration may underlie both cognitive loss and also sleep and EEG changes; this hypothesis would predict that sleep and EEG markers for mild dementia diagnosis will also correlate highly with cognitive loss due to underlying organic changes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH033688-07
Application #
3375435
Study Section
(LCRB)
Project Start
1979-12-01
Project End
1988-03-31
Budget Start
1986-04-01
Budget End
1987-03-31
Support Year
7
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
Schools of Medicine
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
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Moe, K E; Prinz, P N; Larsen, L H et al. (1998) Growth hormone in postmenopausal women after long-term oral estrogen replacement therapy. J Gerontol A Biol Sci Med Sci 53:B117-24
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Larsen, L H; Moe, K E; Vitiello, M V et al. (1995) A note on the night-to-night stability of stages 3 + 4 sleep in healthy older adults: a comparison of visual and spectral evaluations of stages 3 + 4 sleep. Sleep 18:7-10
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Prinz, P N (1995) Sleep and sleep disorders in older adults. J Clin Neurophysiol 12:139-46
Troster, A I; Moe, K E; Vitiello, M V et al. (1994) Predicting long-term outcome in individuals at risk for Alzheimer's disease with the Dementia Rating Scale. J Neuropsychiatry Clin Neurosci 6:54-7
Prinz, P N; Larsen, L H; Moe, K E et al. (1994) C STAGE, automated sleep scoring: development and comparison with human sleep scoring for healthy older men and women. Sleep 17:711-7
Moe, K E; Larsen, L H; Prinz, P N et al. (1993) Major unipolar depression and mild Alzheimer's disease: differentiation by quantitative tonic REM EEG. Electroencephalogr Clin Neurophysiol 86:238-46

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