Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.604200
Title: A new approach to studying prevalence and incidence of cognitive decline and dementia in older adults with Down Syndrome
Author: Hon, Johnny Sei-Hoe
Awarding Body: University of Cambridge
Current Institution: University of Cambridge
Date of Award: 1998
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Abstract:
The aim of this longitudinal study was to investigate the extent of clinical and psychological changes with age using established diagnostic and neuropsychological instruments in a population-based sample of older people with DS. The effects of various risk factors for Alzheimer's Disease (AD) which have been suggested for the general elderly population were also investigated. This is the first population-based study using established methods to assess cognitive impairments and dementia in the DS population. Changes in memory and other cognitive functions, personality, general mental functioning and daily living skills were assessed using a modified version of the informant interview of the Cambridge Examination for Mental Disorders of the Elderly (CAMDEX) together with a number of well established neuropsychological batteries. Age-related prevalence and incidence rates of dementia varied according to the diagnostic criteria used. Significant differences in cognitive functions were found between younger (30-44 years) and older (45+years) subjects. The older group was also found to show greater cognitive deterioration over the 18-month period. In addition, the results demonstrate the erroneous conclusions which may be reached when samples are drawn from day centres rather than through the present unbiased method of sampling. After chronological age, the apo Σ4 genotype was found to be the most important risk factor for AD in the DS population. Overall, the age-related pattern of presentation and dementia diagnoses differs from that seen in the general elderly population. However, age-specific prevalence and incidence rates of AD and the pattern of cognitive decline were similar though appearing approximately 30-40 years earlier in life in the DS population. The results also suggest that most of the neuropsychological test batteries and diagnostic instruments used in the study are suitable for assessing cognitive functions and cognitive decline in adults with DS. Certain risk factors were found to be more important than others in this population. Possible explanations for these findings are proposed.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.604200  DOI: Not available
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