4.5 Article Proceedings Paper

Trajectory of Cognitive Decline as a Predictor of Psychosis in Early Alzheimer Disease in the Cardiovascular Health Study

Journal

AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY
Volume 19, Issue 2, Pages 160-168

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1097/JGP.0b013e3181e446c8

Keywords

Alzheimer disease; MCI (mild cognitive impairment); psychosis

Funding

  1. NHLBI NIH HHS [N01 HC045133, N01 HC035129, N01-HC-75150, N01 HC085079, N01HC85079, N01HC75150, N01 HC085084, N01 HC055222, N01-HC-85079, N01 HC085086, N01 HC-55222, N01 HC085080, N01 HC085081, N01 HC085082, N01HC55222, U01 HL080295-04, N01 HC085085, U01 HL080295, N01 HC075150, N01 HC015103, N01 HC085083, N01-HC-85086, N01HC85086] Funding Source: Medline
  2. NIA NIH HHS [R01 AG027224-04, AG15928, R01 AG015928, R01 AG015928-02, P50 AG005133, P50 AG005133-210020, R01 AG027224, AG05133, R01 AG020098, AG027224] Funding Source: Medline

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Objective: 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). Design: 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. Setting: Community. Participants: 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-epsilon (APOE) genotyping. Measurements: The 3MS and DSST were administered annually and analyzed using mixed-effects models including APOE4 status. Results: 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. Conclusions: 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. (Am J Geriatr Psychiatry 2011; 19: 160-168)

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