ESTABLISHING THE LIMITS AND CHARACTERISTICS OF NORMAL AGE-RELATED COGNITIVE DECLINE

Citation
K. Ritchie et al., ESTABLISHING THE LIMITS AND CHARACTERISTICS OF NORMAL AGE-RELATED COGNITIVE DECLINE, Revue d'epidemiologie et de sante publique, 45(5), 1997, pp. 373-381
Citations number
18
Categorie Soggetti
Public, Environmental & Occupation Heath
ISSN journal
03987620
Volume
45
Issue
5
Year of publication
1997
Pages
373 - 381
Database
ISI
SICI code
0398-7620(1997)45:5<373:ETLACO>2.0.ZU;2-H
Abstract
Background : Research into ageing-related pathology relies not only on exploration of disease aetiology, but also a clear understanding of t he normal ageing process. The present study aims to examine the charac teristics of elderly subjects who lie on the borderline between normal and pathological ageing. Method : Cognitive functioning is examined u sing computerized neuropsychometric assessment in a population of 833 normal elderly from which a cohort of 397 subjects with sub-clinical c ognitive impairment are followed over three years. Subjects receive a standardized neurological examination and ApoE genotypes are establish ed. Results: Analysis of covariance revealed no cross-sectional age di fferences for syntax comprehension (p = 0.19), articulation (p = 0.46) , semantic matching (p = 0.12), reading (p 0.79), and implicit memory (p = 0.21) while explicit memory, language skills and visuospatial ski lls were found to deteriorate both in the cross-sectional age comparis ons and across time. An overall intellectual ability factor; derived f rom Principal Components Analysis, was found by regression to decline principally in persons with low education, and a high initial Ie level was observed to provide a protective effect over age 75. Persons with higher levels of education show relative stability over time on langu age and secondary memory tasks but deteriorate as rapidly as persons w ith low education on visuospatial tasks. Five separate patterns of sub -clinical cognitive deficit were isolated by cluster analysis. Two gro ups, with differing clinical profiles (of which only one manifested th e ApoE4 allele), were found to have an increased risk of developing se nile dementia (OR = 4.4 and 3.9). A third group had a high prevalence of depressive illness, and the remaining two showed very little change . Conclusion : Ageing does not affect all cognitive functions uniforml y; a high initial education level slowing rate of decline for certain tasks. Separate patterns of cognitive change are observed in early sen ile dementia, benign change and changes related to depressive illness. Results suggest the need for more stringent selection of normal contr ol groups.