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DOI: 10.1177/0891988703261994 Sleep/Wake Disruption in Alzheimers Disease: APOE Status and Longitudinal CourseNational Institute of Aging Alzheimers Disease Core Center, Palo Alto VA Health Care System (151Y), 3801 Miranda Avenue, Palo Alto, CA 94304yesavage{at}stanford.edu
Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California
Palo Alto Veterans Affairs Health Care System, Palo Alto, California; Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California
Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California
Palo Alto Veterans Affairs Health Care System, Palo Alto, California; Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California
Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California Disturbed sleep is a major clinical problem in Alzheimers disease (AD). Apolipoprotein 4 (APOE 4) carrier status may increase risk of AD, yet there are no data on relations between APOE status and progression of sleep disturbance in AD. The objective of this study was to determine if sleep parameters in AD patients change over time as a function of APOE carrier status. Forty-four community-dwelling AD patients with diagnosis of probable AD were followed from early stages of disease. Their sleep/wake parameters were compared according to APOE status. For APOE 4 carriers, only wake after sleep onset (WASO) increased in association with lower cognitive function as indicated by the Mini-Mental State Examination (MMSE); for non-4 subjects, increases in WASO and declines in total sleep time, sleep efficiency, and the amplitude of the rest/activity circadian rhythm over time were associated with lower performance on the MMSE. In these data, APOE status was associated with the progression of sleep/wake disturbances in AD. Overall, there was greater deterioration on sleep parameters in patients negative for the 4 allele.
Key Words: Alzheimers disease dementia severity longitudinal studies sleep/wake disturbances circadian rhythm apolipoprotein
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