Evidence map›Paper›PMID 30753650›Full record

Trial reportSleep2019

Strengthening sleep-autonomic interaction via acoustic enhancement of slow oscillations.

Daniela Grimaldi, Nelly A Papalambros, Kathryn J Reid, Sabra M Abbott, Roneil G Malkani, Maged Gendy, Marta Iwanaszko, Rosemary I Braun, Daniel J Sanchez, Ken A Paller and 1 more

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Sleep, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.3field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 77 citations in OpenAlex.

  1. Trial
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  4. Acoustic enhancement of sleep slow oscillations in mild cognitive impairment.Annals of clinical and translational neurology · 2019
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Daniela GrimaldiDepartment of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Nelly A PapalambrosDepartment of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Kathryn J ReidDepartment of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Sabra M AbbottDepartment of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Roneil G MalkaniDepartment of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Maged GendyDepartment of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Marta IwanaszkoBiostatistics Division, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Rosemary I BraunBiostatistics Division, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Daniel J SanchezSRI International, Menlo Park, CA.
Ken A PallerDepartment of Psychology, Northwestern University, Evanston, IL.
Phyllis C ZeeDepartment of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Northwestern University · USSRI International · US

Funding

TRAINING PROGRAM IN THE NEUROSCIENCE OF HUMAN COGNITIONT32NS047987 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Rodrigo M Braga, Christina Maria Zelano · 2006 to 2026
$5.6M
NINDS NIH HHS T32 NS047987
6 · The paper itself

Abstract

Slow-wave sleep (SWS) is important for overall health since it affects many physiological processes including cardio-metabolic function. Sleep and autonomic nervous system (ANS) activity are closely coupled at anatomical and physiological levels. Sleep-related changes in autonomic function are likely the main pathway through which SWS affects many systems within the body. There are characteristic changes in ANS activity across sleep stages. Notably, in non-rapid eye-movement sleep, the progression into SWS is characterized by increased parasympathetic activity, an important measure of cardiovascular health. Experimental manipulations that enhance slow-wave activity (SWA, 0.5-4 Hz) can improve sleep-mediated memory and immune function. However, effects of SWA enhancement on autonomic regulation have not been investigated. Here, we employed an adaptive algorithm to deliver 50 ms sounds phase-locked to slow-waves, with regular pauses in stimulation (~5 s ON/~5 s OFF), in healthy young adults. We sought to determine whether acoustic enhancement of SWA altered parasympathetic activity during SWS assessed with heart rate variability (HRV), and evening-to-morning changes in HRV, plasma cortisol, and blood pressure. Stimulation, compared with a sham condition, increased SWA during ON versus OFF intervals. This ON/OFF SWA enhancement was associated with a reduction in evening-to-morning change of cortisol levels and indices of sympathetic activity. Furthermore, the enhancement of SWA in ON intervals during sleep cycles 2-3 was accompanied by an increase in parasympathetic activity (high-frequency, HRV). Together these findings suggest that acoustic enhancement of SWA has a positive effect on autonomic function in sleep. Approaches to strengthen brain-heart interaction during sleep could have important implications for cardiovascular health.

Indexed as

Acoustic StimulationAdolescentAdultBlood PressureBrainBrain WavesCross-Over StudiesElectroencephalographyFemaleHeart RateHumansMaleSleep, Slow-WaveSleep StagesYoung Adultacoustic stimulationautonomic nervous systemparasympathetic activitysleepslow wave activity

Identifiers

PMID30753650
PMCPMC7729207
OpenAlexW2912085835

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.