Evidence map›Paper›PMID 41929593›Full record

ArticleFrontiers in neurology

Cervical vestibular evoked myogenic potential asymmetry, but not amplitude, differentiates vestibular migraine during prolonged unidirectional visual motion.

Elvira Cortese, Huseyin Nezih Ozdemir, Anca-Diana Grigore, Patricia Castro, Nehzat Koohi, Diego Kaski

Abstract read
In one paragraph

Article in Frontiers in neurology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Elvira CorteseSENSE Research Unit, Department of Clinical and Movement Neurosciences, Institute of Neurology, University College London, London, United Kingdom.
Huseyin Nezih OzdemirSENSE Research Unit, Department of Clinical and Movement Neurosciences, Institute of Neurology, University College London, London, United Kingdom.
Anca-Diana GrigoreSENSE Research Unit, Department of Clinical and Movement Neurosciences, Institute of Neurology, University College London, London, United Kingdom.
Patricia CastroSENSE Research Unit, Department of Clinical and Movement Neurosciences, Institute of Neurology, University College London, London, United Kingdom.
Nehzat KoohiSENSE Research Unit, Department of Clinical and Movement Neurosciences, Institute of Neurology, University College London, London, United Kingdom.
Diego KaskiSENSE Research Unit, Department of Clinical and Movement Neurosciences, Institute of Neurology, University College London, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Vestibular migraine (VM) is the leading cause of episodic vestibular complaints. It arises from altered brain states that disrupt sensory processing. A reliance on clinical history for diagnosis highlights the need for bedside biomarkers, particularly in emergency settings where misdiagnosis is common. Methods: In this cross-sectional study, 30 VM patients (median-age = 40.5; 27 females) from University College London vestibular clinics and 30 age-gender matched healthy controls (median-age = 32.5; 27 females) were recruited, between May 2024 and October 2025. Cervical Vestibular Evoked Myogenic Potential (cVEMP) responses were measured before and after a Results: Mixed linear modeling (MLM) showed no significant effects of group, condition or ear on cVEMP amplitude (all Conclusion: Prolonged unidirectional visual stimulation does not significantly affect cVEMP amplitude responses in VM, limiting its value as a differential diagnostic tool. The need to further explore asymmetry and interaural/interhemispheric sensory integration in VM is underscored.

Indexed as

biomarkerscervical vestibular evoked myogenic potentialvestibular migrainevirtual realityvisual stimulationvisuo-vestibular interactions

Identifiers

PMID41929593
PMCPMC13040205

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