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Cognitive decline in patients with familial Alzheimer's disease associated with E280a presenilin-1 mutation: a longitudinal study.

Authors :
Rosselli MC
Ardila AC
Moreno SC
Standish VC
Arango-Lasprilla JC
Tirado VM
Ossa JM
Goate AM
Kosik KS
Lopera F
Source :
Journal of clinical and experimental neuropsychology [J Clin Exp Neuropsychol] 2000 Aug; Vol. 22 (4), pp. 483-95.
Publication Year :
2000

Abstract

Few longitudinal studies have been carried out to investigate the cognitive decline in early onset of familial Alzheimer's disease (FAD). In this study 12 patients with FAD (M age = 49.61 years, SD = 4.99), 10 patients with sporadic Alzheimer's disease (SAD) (M age = 71.40, SD =10.00), and 15 matched normal controls (M age = 45.01, SD = 7.24) were selected. A comprehensive neuropsychological battery was administered three times over a period of 18 months. Individuals designated as FAD met the criteria for dementia and were positive for the E280A presenilin 1 mutation. Participants with SAD met the criteria for dementia and were negative for the E280A presenilin 1 mutation. Normal control participants were the FAD patients' relatives, who were negative for the mutation. Two groups of neuropsychological instruments were administered: (1) The Consortium to Establish a Registry for Alzheimer's Disease (CERAD) neuropsychological test battery, and (2) additional neuropsychological tests of abstraction and constructional abilities. Patients with FAD were significantly impaired on all measures at the first examination except for reading of words. While the performance of the normal controls remained unchanged over the 18 months for most neuropsychological tests, the patients with FAD displayed a decline in verbal memory, language, constructional and abstraction tests. The greatest decline was observed on the Mini-Mental State Exam scores. Patients with SAD demonstrated a similar pattern of cognitive decline, but the decline was faster in FAD than in SAD participants.

Details

Language :
English
ISSN :
1380-3395
Volume :
22
Issue :
4
Database :
MEDLINE
Journal :
Journal of clinical and experimental neuropsychology
Publication Type :
Academic Journal
Accession number :
10923058
Full Text :
https://doi.org/10.1076/1380-3395(200008)22:4;1-0;FT483