Project: Research project

Project Details


An epidemiologic study of Alzheimer's disease (AD) based on a large
population [that of the Saquenay-Lac-Saint-Jean (SLSJ) region of Quebec]
with several unique and important features, including a computerized
population database and one of the world's largest aluminum refineries, is
proposed. The first phase of this study has 5 aims: (1) to validate a key
informant ascertainment methodology for identifying cases of AD by means of
a prevalence survey of 2 geographic regions in SLSJ; (2) to estimate age-
and sex-specific prevalence rates of dementia and AD; (3) to follow
prevalent cases in order to confirm diagnoses clinically and through
autopsy; (4) to identify a fixed cohort of approximately 1,900 non-demented
individuals that will be utilized in incidence, risk factor and survival
studies; and (5) to perform a population-based case control study of AD
focusing on family history od dementia, education and aluminum as risk
factors. A 3-stage procedure will be utilized to identify cases. Stage 1
will provide initial identification of dementia suspects (by a network of
key informants in year 1; by population screening in years 2 and 3). At
stage 2, suspects will be assessed by specially-trained geriatricians and
general practitioners to determine whether they meet DSM-IIIR criteria for
dementia. At state 3, individuals considered to have dementia will receive
a complete workup to determine the disease responsible for the dementia.
Key informants will include both health professionals and lay persons. The
prevalence survey will utilize a stratified random sample of 2,000
individuals over 64 identified from the socialized health care registry of
Quebec. This sample will be screened, and those individuals who fail the
screen will be evaluated in stages 2 and 3 for dementia. Non-demented
subjects, who will comprise approximately 95% of the sample, will be re-
evaluated and followed for development of dementia. Informants for cases
of possible and probable AD and for 2 matched controls drawn from the non-
demented population will participate in the case-control study. Other non-
demented subjects will be administered the risk factor and family history
questionnaires to study risk factors in relation to later development of
StatusNot started


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