Evidence map›Paper›PMID 37503934›Full record

ArticleSleep2024

Mechanisms underlying the prolonged activation of the genioglossus following arousal from sleep.

Andrew Dawson, Joanne Avraam, Christian L Nicholas, Amanda Kay, Therese Thornton, Nicole Feast, Monika D Fridgant, Fergal J O'Donoghue, John Trinder, Amy S Jordan

Open access · hybridAbstract read
In one paragraph

Article in Sleep, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

10 authors at 1 institution in 1 country.

Andrew DawsonMelbourne School of Psychological Sciences, The University of Melbourne, Parkville, Victoria, Australia.
Joanne AvraamMelbourne School of Psychological Sciences, The University of Melbourne, Parkville, Victoria, Australia.
Christian L NicholasMelbourne School of Psychological Sciences, The University of Melbourne, Parkville, Victoria, Australia.ORCID 0000-0002-3837-3609
Amanda KayMelbourne School of Psychological Sciences, The University of Melbourne, Parkville, Victoria, Australia.
Therese ThorntonMelbourne School of Psychological Sciences, The University of Melbourne, Parkville, Victoria, Australia.
Nicole FeastMelbourne School of Psychological Sciences, The University of Melbourne, Parkville, Victoria, Australia.
Monika D FridgantMelbourne School of Psychological Sciences, The University of Melbourne, Parkville, Victoria, Australia.
Fergal J O'DonoghueDepartment of Respiratory and Sleep Medicine and Institute for Breathing and Sleep, Austin Health, Heidelberg, Victoria, Australia.
John TrinderMelbourne School of Psychological Sciences, The University of Melbourne, Parkville, Victoria, Australia.
Amy S JordanMelbourne School of Psychological Sciences, The University of Melbourne, Parkville, Victoria, Australia.ORCID 0000-0001-8561-9766
The University of Melbourne · AU

Funding

Australian Research Council DP160101398
6 · The paper itself

Abstract

STUDY

objectivesTransient arousal from sleep has been shown to elicit a prolonged increase in genioglossus muscle activity that persists following the return to sleep and which may protect against subsequent airway collapse. We hypothesized that this increased genioglossal activity following return to sleep after an arousal is due to persistent firing of inspiratory-modulated motor units (MUs) that are recruited during the arousal.

methodsThirty-four healthy participants were studied overnight while wearing a nasal mask with pneumotachograph to measure ventilation and with 4 intramuscular genioglossus EMG electrodes. During stable N2 and N3 sleep, auditory tones were played to induce brief (3-15s) AASM arousals. Ventilation and genioglossus MUs were quantified before the tone, during the arousal and for 10 breaths after the return to sleep.

resultsA total of 1089 auditory tones were played and gave rise to 239 MUs recorded across arousal and the return to sleep in 20 participants (aged 23 ± 4.2 years and BMI 22.5 ± 2.2 kg/m2). Ventilation was elevated above baseline during arousal and the first post-arousal breath (p < .001). Genioglossal activity was elevated for five breaths following the return to sleep, due to increased firing rate and recruitment of inspiratory modulated MUs, as well as a small increase in tonic MU firing frequency.

conclusionsThe sustained increase in genioglossal activity that occurs on return to sleep after arousal is primarily a result of persistent activity of inspiratory-modulated MUs, with a slight contribution from tonic units. Harnessing genioglossal activation following arousal may potentially be useful for preventing obstructive respiratory events.

Indexed as

Sleep Apnea, ObstructiveArousalElectromyographyHumansRespirationSleepawakeningobstructive sleep apneapharyngeal dilator musclesupper airway

Identifiers

PMID37503934
PMCPMC10782491
OpenAlexW4385331457

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.