Visual Motion Sensitivity in Vestibular Migraine.
Otol Neurotol 2026 Jun 03. [Online ahead of print]

Abstract

OBJECTIVE

To quantitatively assess visual motion sensitivity in vestibular migraine (VM).

STUDY DESIGN

Cohort study.

SETTING

Single institution.

PATIENTS

Prospective cohort of individuals with VM and healthy controls.

INTERVENTIONS

Subjects rated visually induced symptoms while watching 20 videos with varying degrees of optical flow. After each video, participants rated the intensity of their predominant symptom (headache, dizziness, nausea, or fogginess) on a 5-point Likert scale.

MAIN OUTCOME MEASURES

The primary outcome was a composite symptom score (sum of ratings), which was compared with other patient-reported outcome measures, including (1) Dizziness Handicap Inventory, (2) VM-Patient Assessment Tool and Handicap Inventory, and (3) Visual Vertigo Analog Scale, among other headache, cognitive, and psychometric questionnaires.

RESULTS

The study enrolled 17 participants with VM and 19 healthy controls. The rate of visual motion sensitivity (any symptom) was significantly higher in the VM arm [71.9% vs. 13.7% in controls, X2(4, 705)=245.6, P<0.001]. Composite symptom scores were significantly higher in the VM arm (43.9±13.9 vs. 23.6±6.3 in controls, U=304.0, P<0.001) and significantly correlated with symptom-related measures (P<0.001 for each). Visual Vertigo Analog Scale correlated with composite scores within the VM arm (P<0.001) and the control arm (P=0.01, although not significant after Bonferroni correction).

CONCLUSIONS

Visual motion sensitivity is more frequent in those with VM than in healthy controls, and symptom scores correlated with other established patient-reported outcome measures, especially the Visual Vertigo Analog Scale. Visual motion sensitivity is a distinct and measurable feature of VM and can inform disease severity and treatment response.

Authors+Show Affiliations

Bourdillon AT0000-0001-5111-7450Department of Otolaryngology-Head & Neck Surgery, University of California-San Francisco, San Francisco, CA.
Allen JW0000-0002-5274-1105Department of Radiology and Imaging Sciences, Indiana University, Indianapolis, IN.
Smith JLDepartment of Radiology and Imaging Sciences, Emory University School of Medicine.
Ahluwalia VGeorgia Institute of Technology.
Gore RK0000-0002-8012-1579Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University. Shepherd Center, Atlanta, GA.
Sharon JD0000-0003-4892-5064Department of Otolaryngology-Head & Neck Surgery, University of California-San Francisco, San Francisco, CA.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

42235082