Evidence map›Paper›PMID 37983193›Full record

ArticleThe Journal of physiology2023

Regional associations between inspiratory tongue dilatory movement and genioglossus activity during wakefulness in people with obstructive sleep apnoea.

Lauriane Jugé, Angela Liao, Jade Yeung, Fiona L Knapman, Christopher Bull, Peter G R Burke, Elizabeth C Brown, Simon C Gandevia, Danny J Eckert, Jane E Butler and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Tongue blade neuromuscular junction defects in old F344 rats.Respiratory physiology & neurobiology · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Lauriane JugéNeuroscience Research Australia, Sydney, New South Wales, Australia.
Angela LiaoNeuroscience Research Australia, Sydney, New South Wales, Australia.
Jade YeungNeuroscience Research Australia, Sydney, New South Wales, Australia.ORCID 0000-0002-9705-2450
Fiona L KnapmanNeuroscience Research Australia, Sydney, New South Wales, Australia.ORCID 0000-0003-0829-5934
Christopher BullNeuroscience Research Australia, Sydney, New South Wales, Australia.ORCID 0009-0003-5151-2081
Peter G R BurkeNeuroscience Research Australia, Sydney, New South Wales, Australia.
Elizabeth C BrownNeuroscience Research Australia, Sydney, New South Wales, Australia.
Simon C GandeviaNeuroscience Research Australia, Sydney, New South Wales, Australia.ORCID 0000-0002-1345-3821
Danny J EckertNeuroscience Research Australia, Sydney, New South Wales, Australia.ORCID 0000-0003-3503-2363
Jane E ButlerNeuroscience Research Australia, Sydney, New South Wales, Australia.ORCID 0000-0002-5834-8152
Lynne E BilstonNeuroscience Research Australia, Sydney, New South Wales, Australia.ORCID 0000-0001-8250-9019
UNSW Sydney · AUNeuroscience Research Australia · AUFlinders University · AUPrince of Wales Hospital · AU

Funding

National Health & Medical Research Council (NHMRC) of Australia APP1042646National Health & Medical Research Council (NHMRC) of Australia APP1058974National Health & Medical Research Council (NHMRC) of Australia APP1077934National Health & Medical Research Council (NHMRC) of Australia APP1078061National Health & Medical Research Council (NHMRC) of Australia APP1196261
6 · The paper itself

Abstract

Inspiratory tongue dilatory movement is believed to be mediated via changes in neural drive to genioglossus. However, this has not been studied during quiet breathing in humans. Therefore, this study investigated this relationship and its potential role in obstructive sleep apnoea (OSA). During awake supine quiet nasal breathing, inspiratory tongue dilatory movement, quantified with tagged magnetic resonance imaging, and inspiratory phasic genioglossus EMG normalised to maximum EMG were measured in nine controls [apnoea-hypopnea index (AHI) ≤5 events/h] and 37 people with untreated OSA (AHI >5 events/h). Measurements were obtained for 156 neuromuscular compartments (85%). Analysis was adjusted for nadir epiglottic pressure during inspiration. Only for 106 compartments (68%) was a larger anterior (dilatory) movement associated with a higher phasic EMG [mixed linear regression, beta = 0.089, 95% CI [0.000, 0.178], t(99) = 1.995, P = 0.049, hereafter EMG↗/mvt↗]. For the remaining 50 (32%) compartments, a larger dilatory movement was associated with a lower phasic EMG [mixed linear regression, beta = -0.123, 95% CI [-0.224, -0.022], t(43) = -2.458, P = 0.018, hereafter EMG↘/mvt↗]. OSA participants had a higher odds of having at least one decoupled EMG↘/mvt↗ compartment (binary logistic regression, odds ratio [95% CI]: 7.53 [1.19, 47.47] (P = 0.032). Dilatory tongue movement was minimal (>1 mm) in nearly all participants with only EMG↗/mvt↗ compartments (86%, 18/21). These results demonstrate that upper airway dilatory mechanics cannot be predicted from genioglossus EMG, particularly in people with OSA. Tongue movement associated with minimal genioglossus activity suggests co-activation of other airway dilator muscles. KEY POINTS: Inspiratory tongue movement is thought to be mediated through changes in genioglossus activity. However, it is unknown if this relationship is altered by obstructive sleep apnoea (OSA). During awake supine quiet nasal breathing, inspiratory tongue movement, quantified with tagged magnetic resonance imaging (MRI), and inspiratory phasic genioglossus EMG normalised to maximum EMG were measured in four tongue compartments of people with and without OSA. Larger tongue anterior (dilatory) movement was associated with higher phasic genioglossus EMG for 68% of compartments. OSA participants had an ∼7-times higher odds of having at least one compartment for which a larger anterior tongue movement was not associated with a higher phasic EMG than controls. Therefore, higher genioglossus phasic EMG does not consistently translate into tongue dilatory movement, particularly in people with OSA. Large dilatory tongue movements can occur despite minimal genioglossus inspiratory activity, suggesting co-activation of other pharyngeal muscles.

Indexed as

Sleep Apnea, ObstructiveWakefulnessElectromyographyHumansMovementPharyngeal MusclesTongueintramuscular EMGmagnetic resonance imagingrespiratory physiologysleep disordered breathingupper airway

Identifiers

PMID37983193
PMCPMC10953361
OpenAlexW4388852222

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.