The human vestibular cortex: functional anatomy of OP2, its connectivity and the effect of vestibular disease

Author:

Ibitoye Richard T1234ORCID,Mallas Emma-Jane1256ORCID,Bourke Niall J12,Kaski Diego78,Bronstein Adolfo M34,Sharp David J12569

Affiliation:

1. Computational , Cognitive and Clinical Neuroimaging Laboratory, Department of Brain Sciences, , London W12 0NN, United Kingdom

2. Imperial College London , Cognitive and Clinical Neuroimaging Laboratory, Department of Brain Sciences, , London W12 0NN, United Kingdom

3. Neuro-otology Unit , Department of Brain Sciences, , London W6 8RP, United Kingdom

4. Imperial College London , Department of Brain Sciences, , London W6 8RP, United Kingdom

5. UK Dementia Research Institute , Care Research & Technology Centre, , London W12 0BZ, United Kingdom

6. Imperial College London , Care Research & Technology Centre, , London W12 0BZ, United Kingdom

7. Department of Clinical and Motor Neurosciences , Centre for Vestibular and Behavioural Neurosciences, , London WC1N 3BG, United Kingdom

8. University College London , Centre for Vestibular and Behavioural Neurosciences, , London WC1N 3BG, United Kingdom

9. Centre for Injury Studies, Imperial College London , London SW7 2AZ, United Kingdom

Abstract

Abstract Area OP2 in the posterior peri-sylvian cortex has been proposed to be the core human vestibular cortex. We investigated the functional anatomy of OP2 and adjacent areas (OP2+) using spatially constrained independent component analysis (ICA) of functional magnetic resonance imaging (fMRI) data from the Human Connectome Project. Ten ICA-derived subregions were identified. OP2+ responses to vestibular and visual motion were analyzed in 17 controls and 17 right-sided vestibular neuritis patients who had previously undergone caloric and optokinetic stimulation during fMRI. In controls, a posterior part of right OP2+ showed: (i) direction-selective responses to visual motion and (ii) activation during caloric stimulation that correlated positively with perceived self-motion, and negatively with visual dependence and peak slow-phase nystagmus velocity. Patients showed abnormal OP2+ activity, with an absence of visual or caloric activation of the healthy ear and no correlations with vertigo or visual dependence—despite normal slow-phase nystagmus responses to caloric stimulation. Activity in a lateral part of right OP2+ correlated with chronic visually induced dizziness in patients. In summary, distinct functional subregions of right OP2+ show strong connectivity to other vestibular areas and a profile of caloric and visual responses, suggesting a central role for vestibular function in health and disease.

Funder

UK Medical Research Council

Dunhill Medical Trust

Imperial National Institute for Health Research

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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