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Effect of 1 night of total sleep deprivation on cerebrospinal fluid β-amyloid 42 in healthy middle-aged men: a randomized clinical trial

Authors

Ooms, Sharon, Overeem, Sebastiaan, Besse, Kees, Rikkert, Marcel Olde, Verbeek, Marcel, Claassen, Jurgen A. H. R.

Journal

JAMA Neurology, Volume: 71, No.: 8, Pages.: 971-977

Year of Publication

2014

Abstract

Importance: Increasing evidence suggests a relationship between poor sleep and the risk of developing Alzheimer disease. A previous study found an effect of sleep on β-amyloid (Aβ), which is a key protein in Alzheimer disease pathology.; Objective: To determine the effect of 1 night of total sleep deprivation on cerebrospinal fluid Aβ42 protein levels in healthy middle-aged men.; Design, Setting, and Participants: The Alzheimer, Wakefulness, and Amyloid Kinetics (AWAKE) study at the Radboud Alzheimer Center, a randomized clinical trial that took place between June 1, 2012, and October 1, 2012. Participants were cognitively normal middle-aged men (40-60 years of age) with normal sleep (n = 26) recruited from the local population.; Interventions: Participants were randomized to 1 night with unrestricted sleep (n = 13) or 1 night of total sleep deprivation (24 hours of wakefulness) (n = 13).; Main Outcomes and Measures: Sleep was monitored using continuous polysomnographic recording from 3 pm until 10 am. Cerebrospinal fluid samples were collected using an intrathecal catheter at defined times to compare cerebral Aβ42 concentrations between evening and morning.; Results: A night of unrestricted sleep led to a 6% decrease in Aβ42 levels of 25.3 pg/mL (95% CI [0.94, 49.6], P = .04), whereas sleep deprivation counteracted this decrease. When accounting for the individual trajectories of Aβ42 over time, a difference of 75.8 pg/mL of Aβ42 was shown between the unrestricted sleep and sleep deprivation group (95% CI [3.4, 148.4], P = .04). The individual trajectories of evening and morning Aβ42 concentrations differed between the unrestricted sleep and sleep deprivation groups (P = .04) in contrast to stable Aβ40, tau, and total protein levels.; Conclusions and Relevance: Sleep deprivation, or prolonged wakefulness, interferes with a physiological morning decrease in Aβ42. We hypothesize that chronic sleep deprivation increases cerebral Aβ42 levels, which elevates the risk of Alzheimer disease.; Trial Registration: clinicaltrials.gov Identifier: NCT01194713.;

Bibtex Citation

@article{Ooms_2014, doi = {10.1001/jamaneurol.2014.1173}, url = {http://dx.doi.org/10.1001/jamaneurol.2014.1173}, year = 2014, month = {aug}, publisher = {American Medical Association ({AMA})}, volume = {71}, number = {8}, pages = {971}, author = {Sharon Ooms and Sebastiaan Overeem and Kees Besse and Marcel Olde Rikkert and Marcel Verbeek and Jurgen A. H. R. Claassen}, title = {Effect of 1 Night of Total Sleep Deprivation on Cerebrospinal Fluid $upbeta$-Amyloid 42 in Healthy Middle-Aged Men}, journal = {{JAMA} Neurology} }

Keywords

adult, cerebral, cerebrospinal fluid, humans, levels, male, middle aged, peptide fragments, physiology, polysomnography, sleep, sleep deprivation, time factors

Countries of Study

Netherlands

Types of Dementia

Alzheimer’s Disease

Types of Study

Randomised Controlled Trial

Type of Outcomes

Other

Type of Interventions

Risk Factor Modification

Risk Factor Modifications

General population health promotion