Brain Advance Access originally published online on March 3, 2004
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Brain, Vol. 127, No. 5, 1061-1074, 2004
© 2004 Guarantors of Brain
doi: 10.1093/brain/awh129
Disrupted daily activity/rest cycles in relation to daily cortisol rhythms of home-dwelling patients with early Alzheimer’s dementia
1 Department of Anatomy, Cambridge University, Cambridge CB2 3DY, UK, 2 Netherlands Institute for Brain Research and VU University Medical Center, Amsterdam, The Netherlands, 3 MRC-CBU, Cambridge CB2 2EF and 4 MRC-LMB, Neurobiology Division, Cambridge, UK
Correspondence to: M. H. Hastings, MRC Laboratory of Molecular Biology, Neurobiology Division, Hills Road, Cambridge CB2 2QH, UK E-mail: mha{at}mrc-lmb.cam.ac.uk
Disturbed sleep cycles are the principal cause of institutionalization in dementia, and therefore represent a major clinical problem. They may arise from dysfunction within the circadian clock of the hypothalamus that times and consolidates wakefulness, or from neuropathology in output pathways and/or target sites of the clock specifically controlling sleep and wakefulness. To determine the relationship of disturbed activity cycles to other circadian clock-controlled rhythms, cross-sectional and longitudinal actigraphy and serial sampling of saliva were used to compare the impact of early Alzheimer’s dementia on activity/rest and cortisol rhythms in home-dwelling subjects. Mildly demented subjects had daily activity rhythms comparable to those of healthy age-matched subjects. Moderately demented subjects exhibited a range of disturbances of the activity/rest cycle, with reduced stability, increased fragmentation and loss of amplitude. Within the moderately demented group, however, the degree of circadian disruption was not correlated with the individual severity of dementia. All groups of subjects, mild, moderate with normal activity cycles and moderate with abnormal activity cycles, exhibited robust daily profiles of salivary cortisol, with highest levels in the morning (08:00 h) and an evening nadir (20:00–24:00 h). Salivary cortisol levels tended to be higher in the moderately demented subjects in the afternoon, but this effect was not specific to those with abnormal activity/rest patterns. The actimetric data confirm that deterioration of activity/rest cycles is a common and progressive feature in home-dwelling Alzheimer’s patients, occurring early in the disease but after the measurable onset of dementia. The maintenance of highly rhythmic daily cortisol profiles in association with disturbed activity profiles, both on an individual and on a group basis, demonstrates that loss of circadian control to activity/rest cycles is not a consequence of global circadian disruption in early dementia. Rather, pathology may develop in discrete elements of the circadian clockwork and/or its output systems that control activity/rest, sleep and wakefulness. Further characterization of this pathology will facilitate more effective management of sleep patterns in home-dwelling demented patients.
Key Words: actimetry; body clock; circadian; cortisol; sleep
Abbreviations: ANOVA = analysis of variance; HPA = hypothalamo-pituitary-adrenal; IS = inter-daily stability; IV = intra-daily variability; MMSE = Mini-Mental State Examination; NPCRA = non-parametric circadian rhythm analysis; PSG = polysomnographic; RA = rhythm analysis; SCN = suprachiasmatic nuclei of the hypothalamus
Received July 28, 2003. Revised November 4, 2003. Accepted December 21, 2003.
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  D. G. Harper, E. G. Stopa, V. Kuo-Leblanc, A. C. McKee, K. Asayama, L. Volicer, N. Kowall, and A. Satlin Dorsomedial SCN neuronal subpopulations subserve different functions in human dementia Brain, June 1, 2008; 131(6): 1609 - 1617. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 P. N. Pallier, E. S. Maywood, Z. Zheng, J. E. Chesham, A. N. Inyushkin, R. Dyball, M. H. Hastings, and A. Jennifer Morton Pharmacological Imposition of Sleep Slows Cognitive Decline and Reverses Dysregulation of Circadian Gene Expression in a Transgenic Mouse Model of Huntington's Disease J. Neurosci., July 18, 2007; 27(29): 7869 - 7878. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 D. L. Woods and J. L. Martin Cortisol and Wake Time in Nursing Home Residents With Behavioral Symptoms of Dementia Biol Res Nurs, July 1, 2007; 9(1): 21 - 29. [Abstract] [PDF]
|
|
|
|
 |
|
 H. M. Prosser, A. Bradley, J. E. Chesham, F. J. P. Ebling, M. H. Hastings, and E. S. Maywood Prokineticin receptor 2 (Prokr2) is essential for the regulation of circadian behavior by the suprachiasmatic nuclei PNAS, January 9, 2007; 104(2): 648 - 653. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
L. Esposito, J. Raber, L. Kekonius, F. Yan, G.-Q. Yu, N. Bien-Ly, J. Puolivali, K. Scearce-Levie, E. Masliah, and L. Mucke Reduction in mitochondrial superoxide dismutase modulates Alzheimer's disease-like pathology and accelerates the onset of behavioral changes in human amyloid precursor protein transgenic mice. J. Neurosci., May 10, 2006; 26(19): 5167 - 5179. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. J. Morton, N. I. Wood, M. H. Hastings, C. Hurelbrink, R. A. Barker, and E. S. Maywood Disintegration of the Sleep-Wake Cycle and Circadian Timing in Huntington's Disease J. Neurosci., January 5, 2005; 25(1): 157 - 163. [Abstract] [Full Text] [PDF]
|
|