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临床试验/NCT03576664
NCT03576664已完成早期 1 期

Effects of Sleep Deprivation and Adrenergic Inhibition on Glymphatic Flow in Humans

Gitte Moos Knudsen1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2018年8月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
发起方
入组人数
22
试验地点
1
主要终点
Measure EEG slow wave activity during Magnetic Resonance imaging and compare Carvedilol with placebo to see how sleep is affected by the treatment

研究概览

简要总结

The project is aimed at identifying how the adrenergic antagonist 'carvedilol' modulates the effects of sleep deprivation in healthy volunteers. The study is a double-blind, randomized, placebo-controlled, cross-over study. Investigators will include 20 healthy volunteers who will undergo three functional magnetic resonance (fMRI) imaging sessions, one at baseline, and two after sleep deprivation (one night without sleep). The two sleep-deprivation scans are performed in a randomized order where subjects receive placebo or carvedilol, in a within-subject, cross-over study design.

The following domains will be described: 1) fMRI imaging of cerebrospinal fluid (CSF) pulsations (glymphatic flow) in the human brain, performed by a combination of fMRI protocols that includes structural (T1, T2, diffusion weighted) and functional (multiband/fast imaging, spectroscopy) imaging. 2) fMRI imaging during wakefulness and sleep are determined by simultaneous electroencephalographic (EEG) recordings. 3) The effects of sleep deprivation on the fMRI derived glymphatic flow signal. 4) The effects of the adrenergic antagonist carvedilol on fMRI measurements and sleep intensity. 5) Quantification of cognitive performance before and after a nap in the MRI. Cognitive testing includes: assessments of visual attention, reaction time, paired-associative memory, working memory, emotional recognition and subjective ratings of sleepiness and mood.

详细描述

Aims and background:

Sleep is a universal biological process. Lack of, or insufficient sleep, has been associated with a range of diseases including obesity, cardiovascular disease, reduced cognition, impaired learning, and increased risk of motor vehicle accidents. Sleep is also associated with neuromolecular alterations in the brain, including reduced firing of arousal maintaining epinephrine and norepinephrine neurons.

A novel molecular function of sleep known as the glymphatic system has recently been described in rodents. This system is specifically activated during non-rapid eye movement (NREM) sleep, and glymphatic flow appear strongly enhanced during sleep when compared to wakefulness. Moreover, it has been shown that adrenergic antagonists enhance glymphatic clearance and flow in rodents. This study aims at applying newly developed functional magnetic resonance imaging (fMRI) protocols to investigate the extent of the glymphatic system non-invasively in humans.

In order for us to quantify the change in glymphatic clearance between sleep and wakefulness, it is necessary to measure the glymphatic process in both vigilance states, requiring that volunteers nap in the MRI scanner. Moreover, to clarify causal relationships, this study will challenge the glymphatic system via adrenergic inhibition. To do so, the investigators will administer the adrenergic antagonist Carvedilol, which can cross the blood-brain barrier. The drug will be perorally administered before a nap in the MRI, in a double blind, placebo controlled manner. To assess sleep quality and function, cognitive testing will be performed before and after the nap in the MRI scanner. Moreover, to distinguish sleep and wakefulness, electroencephalographic (EEG) recordings will be performed during magnetic resonance (MR)-imaging. Because sleep is a strong homeostatic regulated process, sleep quality, duration and timing will be controlled by EEG monitoring, immediately prior to and during the study to ensure that data is intra- and inter-individually comparable.

Hypotheses:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy volunteer (male or female) between 18 and 35 years.
  • Good sleeper with sleep efficiency above 80%.

排除标准

  • Current or former primary psychiatric disorder in volunteer of first degree relatives (DSM IV Axis I or WHO ICD-10 diagnostic classification).
  • Current or previous neurological disease, severe somatic disease, or the consumption of drugs likely to influence the test results.
  • Claustrophobia or fear of being in an MR-scanner.
  • Alcohol or drug abuse.
  • Regular smoking or nicotine addiction
  • Extreme morning or evening type, or extreme short or long sleeper.
  • Disordered sleep, regular shift-work or extreme tiredness (e.g. Epworth Sleepiness Scale (ESS) > 10).
  • Crossing of multiple time zones within the last 6 months.
  • Extreme use of stimulants such as caffeine.
  • Not adhering to the prescribed sleep-wake schedule before study initiation.
  • Left handedness.
  • Obesity (BMI > 27.5).
  • Non-fluent in Danish or pronounced visual or auditory impairments.
  • Current or past learning disability.
  • Large head size (>59 cm in circumference).
  • Pregnancy
  • Contraindications for MRI (pacemaker, metal implants, etc.).
  • Allergy to the ingredients in the administered drug.
  • Abnormal ECG (e.g. prolonged QT syndrome, etc.)
  • Dizzy when changing from supine to upright position (e.g. postural orthostatic tachycardia syndrome).
  • Mild hypotension (blood pressure below 100/70 mmHg)
  • Hypertension (blood pressure above 140/90 mmHg).

研究组 & 干预措施

Carvedilol first

Experimental

Carvedilol (25 mg) followed by Placebo oral capsule is administered in a crossover manner.

干预措施: Carvedilol 25mg (Drug)

Carvedilol first

Experimental

Carvedilol (25 mg) followed by Placebo oral capsule is administered in a crossover manner.

干预措施: Placebo oral capsule (Drug)

Placebo first

Experimental

Placebo oral capsule followed by Carvedilol (25 mg) is administered in a crossover manner.

干预措施: Carvedilol 25mg (Drug)

Placebo first

Experimental

Placebo oral capsule followed by Carvedilol (25 mg) is administered in a crossover manner.

干预措施: Placebo oral capsule (Drug)

结局指标

主要结局

Measure EEG slow wave activity during Magnetic Resonance imaging and compare Carvedilol with placebo to see how sleep is affected by the treatment

时间窗: Placebo compared to treatment 5±3 days apart.

Measure if fMRI-detected glymphatic flow correlates with subjective sleepiness ratings

时间窗: Measurements collected within the same 1 day

Measure whether Carvedilol improves sleepiness after the MR scan compared to placebo

时间窗: Measurements collected within the same 1 day

Measure fMRI-detected glymphatic flow and whether it correlates with cognitive performance before and after MR imaging

时间窗: Measurements collected within the same 1 day

Measure and compare functional Magnetic Resonance Imaging (fMRI)-detected glymphatic flow in baseline sleep and in sleep-deprived sleep

时间窗: Baseline to follow-up 5±3 days

Measure and compare fMRI-detected glymphatic flow in placebo and carvedilol condition

时间窗: Placebo compared to treatment 5±3 days apart.

Correlate fMRI-detected glymphatic flow with simultaneous detected EEG sleep slow wave activity

时间窗: Nocturnal sleep compared to sleep during Magnetic Resonance scans within same 1 day.

Measure the change in functional Magnetic Resonance Imaging (fMRI)-detected glymphatic flow in wakefulness and sleep at baseline

时间窗: Baseline compared to baseline - within same 1 day

Measure fMRI-detected glymphatic flow and whether correlates with changes in cognitive performance from before to after MR imaging

时间窗: Measurements collected within the same 1 day

Measure whether Carvedilol improves cognitive performance (measurement: psychomotor vigilance test) after the MR scan compared to placebo

时间窗: Measurements collected within the same 1 day

次要结局

  • Measure whether fMRI-detected glymphatic flow is positively correlated with sleep driven structural changes in T2 and diffusion weighted (DWI) images(Measurements collected within the same 1 day)
  • Measure whether the visual attention (measurement: Theory of Visual Attention task) is modulated by sleep-deprivation(Baseline to follow-up 5±3 days)
  • Measure whether fMRI-detected glymphatic flow correlates with simultaneous NREM EEG activity(Measurements collected within the same 1 day)
  • Measure whether fMRI-detected glymphatic flow is spatially correlated with simultaneous EEG NREM slow wave activity(Measurements collected within the same 1 day)
  • Measure whether the visual attention (measurement: Theory of Visual Attention task) is modulated by carvedilol(Placebo compared to treatment 5±3 days apart.)
  • Measure whether emotional memory performance (measurement: emotional word pair task) is modulated by carvedilol(Placebo compared to treatment 5±3 days apart.)
  • Measure whether Carvedilol modulates nocturnal recovery sleep (measurement: EEG slow wave activity) after sleep deprivation(Baseline to follow-up 5±3 days)
  • Measure whether the psychomotor vigilance test is modulated by carvedilol(Placebo compared to treatment 5±3 days apart.)
  • Measure whether emotional memory performance (measurement: emotional word pair task) is modulated by sleep-deprivation(Baseline to follow-up 5±3 days)

研究者

发起方
Gitte Moos Knudsen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Gitte Moos Knudsen

Center director of Center for Integrated Molecular Brain Imaging

Rigshospitalet, Denmark

研究点 (1)

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