Hostname: page-component-cd9895bd7-dk4vv Total loading time: 0 Render date: 2024-12-26T06:29:17.897Z Has data issue: false hasContentIssue false

Mortality and Temporal Course of Probable Alzheimer's Disease: A 5-Year Prospective Study

Published online by Cambridge University Press:  07 January 2005

Barry Reisberg
Affiliation:
Aging and Dementia Research Center, New York University Medical Center, New York, New York, U.S.A.
Steven H. Ferris
Affiliation:
Aging and Dementia Research Center, New York University Medical Center, New York, New York, U.S.A.
Emile H. Franssen
Affiliation:
Aging and Dementia Research Center, New York University Medical Center, New York, New York, U.S.A.
Emma Shulman
Affiliation:
Aging and Dementia Research Center, New York University Medical Center, New York, New York, U.S.A.
Isabel Monteiro
Affiliation:
Aging and Dementia Research Center, New York University Medical Center, New York, New York, U.S.A.
Steven G. Sclan
Affiliation:
Aging and Dementia Research Center, New York University Medical Center, New York, New York, U.S.A.
Gertrude Steinberg
Affiliation:
Aging and Dementia Research Center, New York University Medical Center, New York, New York, U.S.A.
Alan Kluger
Affiliation:
Aging and Dementia Research Center, New York University Medical Center, New York, New York, U.S.A.
Carol Torossian
Affiliation:
Aging and Dementia Research Center, New York University Medical Center, New York, New York, U.S.A.
Mony J. de Leon
Affiliation:
Aging and Dementia Research Center, New York University Medical Center, New York, New York, U.S.A.
Eugene Laska
Affiliation:
Nathan S. Kline Istitute for Psychiatric Research, Orangeburg, New York, U.S.A.
Get access

Abstract

Alzheimer's disease (AD) is asociated with an increased mortality in comparison with aged control populations. The relationship between the clinical and the temporal course of AD has not been well studied over significant intervals. Community residing patients with probable AD (N = 103, 42 men, mean age = 70.2 ± 8.0 years) were studied at baseline on demographic and clinical variables, including measures of global deterioration (Global Deterioration Scale; GDS), mental status and cognition (e.g., Mini-Mental State Examination; MMSE), and functional impairment (Functional Assessment Staging; FAST). Baseline characteristics included a GDS range of Stage 4, 5, or 6 (38.8%, 39.8%, and 21.4% respectively) and a mean MMSE score of 15.4 ± 5.6. The mean follow-up interval was 4.6 ± 1.4 year. Follow-ups were done blind to baseline measures and when necessary were conducted in residential and nursing home settings. Of locatable subjects (n = 95, 92%), 30 (31.6%) were deceased. Survivors (n = 65) had a mean GDS stage of 6.2 ± 0.9 and a mean MMSE score of 5.1 ± 6.9; 51% had MMSE scores of 0. Increased age and male gender, but not baseline clinical dementia variables, increased the risk of death (ps < .01). Change in clinical variables correlated significantly with time elapsed (r = .32, p < .05, for MMSE change, to r = .48, p < .001, for GDS change). Significant variance in temporal change (i.e., time elapsed) was accounted for by change in two of the five clinical measures studied (i.e., GDS and FAST; multiple r = .53). The results support previous estimates of mean duration of the GDS and FAST stages. For subjects with probable AD followed over approximately 5 years, clinical variables changed significantly over time in survivors. However, the majority of temporal variance in the course of AD remains unexplained.

Type
Longitudinal Course
Copyright
© 1996 International Psychogeriatric Association

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)