Article

Trajectory of cognitive decline as a predictor of psychosis in early Alzheimer disease in the cardiovascular health study.

Departments of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.
The American journal of geriatric psychiatry: official journal of the American Association for Geriatric Psychiatry (impact factor: 3.35). 02/2011; 19(2):160-8. DOI:10.1097/JGP.0b013e3181e446c8 pp.160-8
Source: PubMed

ABSTRACT To compare the trajectories of cognitive decline between groups with, and without, the later development of psychotic symptoms during Alzheimer disease (AD) or mild cognitive impairment (MCI).
: The authors examined cognitive function in a new analysis of an existing data set, the Cardiovascular Health Study, an epidemiologic, longitudinal follow-up study. Our analyses examined 9 years of follow-up data.
Community.
The authors examined subjects who were without dementia at study entry, received a diagnosis of AD or MCI during follow-up, and had been rated on the Neuropsychiatric Inventory for the presence of psychosis; 362 participants for the modified Mini-Mental State Examination (3MS) analysis and 350 participants for the digit symbol substitution test (DSST) analysis had sufficient follow-up data and apolipoprotein-∊ (APOE) genotyping.
The 3MS and DSST were administered annually and analyzed using mixed-effects models including APOE4 status.
: Mean 3MS and DSST scores did not differ between AD with psychosis (AD + P) and without psychosis groups at baseline. The 3MS and DSST scores decreased more rapidly in subjects who ultimately developed psychosis.
Individuals who ultimately develop psychosis have more rapid cognitive deterioration during the earliest phases of AD than individuals with AD not developing psychosis. The genetic and other neurobiologic factors leading to the expression of AD + P may exert their effects by acceleration of the neurodegenerative process.

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Keywords

350 participants
 
362 participants
 
AD + P
 
APOE4 status
 
Cardiovascular Health Study
 
digit symbol substitution test
 
earliest phases
 
epidemiologic
 
existing data
 
follow-up data
 
longitudinal follow-up study
 
Mean 3MS
 
mild cognitive impairment
 
modified Mini-Mental State Examination
 
neurodegenerative process
 
Neuropsychiatric Inventory
 
psychosis
 
psychosis groups
 
psychotic symptoms
 
rapid cognitive deterioration