Principal Investigators

    OSORIO, RICARDO S

    Institution

    NEW YORK UNIVERSITY SCHOOL OF MEDICINE

    Contact information of lead PI

    Country

    USA

    Title of project or programme

    Brain Sleep Clearance of Amyloid-Beta Peptides Study (Brain SCRAPS)

    Source of funding information

    NIH (NIA)

    Total sum awarded (Euro)

    416513.7615

    Start date of award

    01/08/2015

    Total duration of award in years

    2

    Keywords

    Acquired Cognitive Impairment... Aging... Alzheimer's Disease... Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)... Behavioral and Social Science... Brain Disorders... Clinical Research... Clinical Research - Extramural... Dementia... Lung... Neurodegenerative... Neurosciences... Sleep Research

    Research Abstract

    ? DESCRIPTION (provided by applicant): Alzheimer’s disease (AD) is a common neurodegenerative disease characterized by the accumulation of amyloid plaques and neurofibrillary tangles. Recent studies support the hypothesis that amyloid beta (Aß) dynamics in the brain are influenced by the sleep-wake cycle, with increases in the production of soluble Aß during wakefulness and decreases during slow wave sleep (SWS). In this model, prior to amyloid deposition, brain soluble Aß levels may be relatively increased in the elderly primarily due to loss of total sleep time and slow wave sleep (SWS) that occur with normal aging and/or secondarily, due to sleep disturbances such as Sleep Disordered Breathing (SDB) or insomnia that are common in late life. We have preliminary evidence showing that: a) SDB advances cognitive decline in normal elderly; b) SDB increases cerebrospinal fluid (CSF) Aß42 levels in middle age adults; and, c) increased CSF Aß42 is associated with reduced SWS in normal elderly. Our goal is to test this hypothesis in 20 cognitively normal elderly with no SDB or brain amyloid (Aim 1), and a group of 22 middle age adults with severe SDB treated with therapeutic continuous positive airway pressure (CPAP) and good treatment compliance (Aim 2). In the elderly group, we will evaluate the relationship between SWS and CSF Aß42/Aß40 ratio in the absence of SDB or amyloid burden (measured with a 18F-florbetaben PET scan). In the middle age group, we will disrupt sleep by withdrawing CPAP on one night and allow participants to sleep with therapeutic CPAP on a second night. A morning lumbar puncture will be performed in both visits to evaluate the effect of disrupting sleep by acute CPAP withdrawal on CSF Aß42 levels. This project will be the first to explore the protective effect of SWS on Aß42 dynamics in a group of elderly subjects as well as the effect of acute sleep disruption by CPAP withdrawal on CSF Aß42 levels in a well- characterized clinical sample of severe middle age obstructive SDB patients. This proposal may identify: 1) evidence of age-related SWS loss effects on CSF Aß42 dynamics; 2) a mechanism by which a highly prevalent sleep disorder may contribute to AD pathology; and, 3) SWS as new therapeutic target for AD prevention.

    Further information available at:

Types: Investments < €500k
Member States: United States of America
Diseases: N/A
Years: 2016
Database Categories: N/A
Database Tags: N/A

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