Evidence map›Paper›PMID 39617808›Full record

ArticleExperimental brain research2024

After the n10: late oVEMP peaks in patients with unilateral vestibular loss and healthy volunteers.

Alyssa C Dyball, Xiao Ping Wu, Belinda Y C Kwok, Chao Wang, Benjamin Nham, Jacob M Pogson, Jonathan H K Kong, Rachael L Taylor, Konrad P Weber, Miriam S Welgampola and 1 more

Abstract read
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Article in Experimental brain research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
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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.

Alyssa C DyballCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, Australia.
Xiao Ping WuAudiology Department, Macquarie University, Sydney, Australia.
Belinda Y C KwokCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, Australia.
Chao WangCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, Australia.
Benjamin NhamCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, Australia.
Jacob M PogsonCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, Australia.
Jonathan H K KongDepartment of Otolaryngology, Royal Prince Alfred Hospital, Sydney, Australia.
Rachael L TaylorDepartment of Physiology, Centre for Brain Research, The University of Auckland, Auckland, New Zealand.
Konrad P WeberDepartments of Neurology and Ophthalmology, University Hospital Zurich, Zurich, Switzerland.
Miriam S WelgampolaCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, Australia.
Sally M RosengrenCentral Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, Australia. sally@srosengren.org.ORCID http://orcid.org/0000-0002-3830-7214

Funding

Faculty of Medicine and Health, University of Sydney SC4245Garnett Passe and Rodney Williams Memorial Foundation SC4104National Health and Medical Research Council GNT1104772
6 · The paper itself

Abstract

The ocular vestibular evoked myogenic potential (oVEMP) is a measure of otolith function. The initial n10 peak follows a contralateral pathway from ipsilateral utricle to contralateral inferior oblique muscle. Following the n10, a series of positive and negative waves are elicited in the inferior oblique, but their characteristics and generators are unknown. This paper therefore investigated the latency, amplitude, and laterality of these late peaks in patients with hearing or vestibular loss compared to healthy volunteers. oVEMPs were elicited to bone-conducted (BC) square wave pulses and air-conducted (AC) clicks in 63 healthy volunteers, 15 patients with profound hearing loss (HL), 45 patients with unilateral vestibular loss (uVL), and 10 patients with bilateral vestibular loss (bVL). In healthy volunteers, up to 5 peaks and troughs were elicited to BC bilaterally. The first two peaks were largest, and amplitude decreased linearly thereafter. In healthy volunteers stimulated with AC clicks and patients with uVL stimulated with either stimulus, the first 2-3 oVEMP waves were significantly larger on the side opposite the healthy/stimulated ear, while the later waves were smaller and had similar amplitude bilaterally. All peaks were absent stimulating ears with no measurable vestibular function. Late peaks were elicited in patients with intact vestibular function regardless of hearing status, demonstrating the vestibular origin of all peaks. Like the clinical n10-p15 waves, the second waves followed a dominant contralateral pathway, while waves 3 onwards appear to have a separate origin and may represent bilateral projections to the extra-ocular muscles.

Indexed as

Vestibular DiseasesVestibular Evoked Myogenic PotentialsAcoustic StimulationAdolescentAdultAgedBone ConductionFemaleFunctional LateralityHealthy VolunteersHumansMaleMiddle AgedReaction TimeYoung AdultCentralExtraocularOriginProjectionVEMP

Identifiers

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Registered trials

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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.