Evidence map›Paper›PMID 33367536›Full record

ArticleBrain : a journal of neurology2021

Vestibular agnosia in traumatic brain injury and its link to imbalance.

Elena Calzolari, Mariya Chepisheva, Rebecca M Smith, Mohammad Mahmud, Peter J Hellyer, Vassilios Tahtis, Qadeer Arshad, Amy Jolly, Mark Wilson, Heiko Rust and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 82 citations in OpenAlex.

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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

12 authors at 5 institutions in 1 country.

Elena CalzolariBrain and Vestibular Group, Neuro-Otology Unit, Department of Brain Sciences, Charing Cross Hospital, Imperial College London, London, W6 8RF, UK.
Mariya ChepishevaBrain and Vestibular Group, Neuro-Otology Unit, Department of Brain Sciences, Charing Cross Hospital, Imperial College London, London, W6 8RF, UK.
Rebecca M SmithBrain and Vestibular Group, Neuro-Otology Unit, Department of Brain Sciences, Charing Cross Hospital, Imperial College London, London, W6 8RF, UK.
Mohammad MahmudBrain and Vestibular Group, Neuro-Otology Unit, Department of Brain Sciences, Charing Cross Hospital, Imperial College London, London, W6 8RF, UK.
Peter J HellyerCentre for Neuroimaging Sciences, King's College London, London WC2R 2LS, UK.
Vassilios TahtisBrain and Vestibular Group, Neuro-Otology Unit, Department of Brain Sciences, Charing Cross Hospital, Imperial College London, London, W6 8RF, UK.
Qadeer ArshadInAmind Laboratory, Department of Neuroscience, Psychology and Behaviour, University of Leicester, Leicester, LE1 7RH, UK.
Amy JollyC3NL, Department of Brain Sciences, Hammersmith Hospital, Imperial College London, London, W12 0NN, UK.
Mark WilsonSt Mary's Hospital Major Trauma Centre, Imperial College Healthcare NHS Trust, London, W2 1NY, UK.
Heiko RustBrain and Vestibular Group, Neuro-Otology Unit, Department of Brain Sciences, Charing Cross Hospital, Imperial College London, London, W6 8RF, UK.
David J SharpC3NL, Department of Brain Sciences, Hammersmith Hospital, Imperial College London, London, W12 0NN, UK.
Barry M SeemungalBrain and Vestibular Group, Neuro-Otology Unit, Department of Brain Sciences, Charing Cross Hospital, Imperial College London, London, W6 8RF, UK.
Charing Cross Hospital · GBHammersmith Hospital · GBImperial College Healthcare NHS Trust · GBUniversity of Leicester · GBWellcome Centre for Human Neuroimaging · GB

Funding

Department of Health ICA-CDRF-2017-03-070Department of Health II-LB-0715-20006Department of Health NIHR-RP-011-048Medical Research Council MR/J004685/1Medical Research Council MR/P006493/1Medical Research Council MR/T023880/1
6 · The paper itself

Abstract

Vestibular dysfunction, causing dizziness and imbalance, is a common yet poorly understood feature in patients with TBI. Damage to the inner ear, nerve, brainstem, cerebellum and cerebral hemispheres may all affect vestibular functioning, hence, a multi-level assessment-from reflex to perception-is required. In a previous report, postural instability was the commonest neurological feature in ambulating acute patients with TBI. During ward assessment, we also frequently observe a loss of vertigo sensation in patients with acute TBI, common inner ear conditions and a related vigorous vestibular-ocular reflex nystagmus, suggesting a 'vestibular agnosia'. Patients with vestibular agnosia were also more unbalanced; however, the link between vestibular agnosia and imbalance was confounded by the presence of inner ear conditions. We investigated the brain mechanisms of imbalance in acute TBI, its link with vestibular agnosia, and potential clinical impact, by prospective laboratory assessment of vestibular function, from reflex to perception, in patients with preserved peripheral vestibular function. Assessment included: vestibular reflex function, vestibular perception by participants' report of their passive yaw rotations in the dark, objective balance via posturography, subjective symptoms via questionnaires, and structural neuroimaging. We prospectively screened 918 acute admissions, assessed 146 and recruited 37. Compared to 37 matched controls, patients showed elevated vestibular-perceptual thresholds (patients 12.92°/s versus 3.87°/s) but normal vestibular-ocular reflex thresholds (patients 2.52°/s versus 1.78°/s). Patients with elevated vestibular-perceptual thresholds [3 standard deviations (SD) above controls' average], were designated as having vestibular agnosia, and displayed worse posturography than non-vestibular-agnosia patients, despite no difference in vestibular symptom scores. Only in patients with impaired postural control (3 SD above controls' mean), whole brain diffusion tensor voxel-wise analysis showed elevated mean diffusivity (and trend lower fractional anisotropy) in the inferior longitudinal fasciculus in the right temporal lobe that correlated with vestibular agnosia severity. Thus, impaired balance and vestibular agnosia are co-localized to the inferior longitudinal fasciculus in the right temporal lobe. Finally, a clinical audit showed a sevenfold reduction in clinician recognition of a common peripheral vestibular condition (benign paroxysmal positional vertigo) in acute patients with clinically apparent vestibular agnosia. That vestibular agnosia patients show worse balance, but without increased dizziness symptoms, explains why clinicians may miss treatable vestibular diagnoses in these patients. In conclusion, vestibular agnosia mediates imbalance in traumatic brain injury both directly via white matter tract damage in the right temporal lobe, and indirectly via reduced clinical recognition of common, treatable vestibular diagnoses.

Indexed as

Postural BalanceAdolescentAdultAgedAgnosiaBrain Injuries, TraumaticDizzinessFemaleHumansMaleMiddle AgedReflex, RightingVestibule, LabyrinthWhite MatterYoung Adultself-motion perceptiontraumatic brain injuryvertigovestibular agnosiavestibular cognition

Identifiers

PMID33367536
PMCPMC7880674
OpenAlexW3114031698

What OpenQuestion holds

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LicenceCC BY
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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.