Four-hour-delayed 3D-FLAIR MRIs in patients with acute unilateral peripheral vestibulopathy

Keun-Tae Kim1, Sangeun Park2, Sun-Uk Lee1,3

  • 1Department of Neurology, Korea University Medical Center, Seoul, South Korea.

Abstract

Insights

Delayed MRI with gadolinium enhancement shows significant findings in nearly half of patients with acute unilateral peripheral vestibulopathy/vestibular neuritis (AUPV/VN). This imaging technique correlates well with neurotologic evaluations, aiding in diagnosis.

Area of Science:

  • Neurology
  • Radiology
  • Otolaryngology

Background:

  • Magnetic Resonance Imaging (MRI) is conventionally used to differentiate acute unilateral peripheral vestibulopathy/vestibular neuritis (AUPV/VN) from similar conditions.
  • The diagnostic value of specialized inner ear MRIs for AUPV/VN requires further investigation.

Purpose of the Study:

  • To evaluate the diagnostic utility of delayed, contrast-enhanced 3D-FLAIR MRI sequences in patients with AUPV/VN.
  • To assess the correlation between MRI findings and neurotologic evaluations in AUPV/VN.

Main Methods:

  • Prospective recruitment of 53 patients diagnosed with AUPV/VN.
  • Standard MRI protocol followed by an axial 3D-fluid-attenuated inversion recovery (3D-FLAIR) sequence 4 hours post-gadolinium injection.
  • Comparison of MRI findings with neurotologic assessments.

Main Results:

  • Gadolinium enhancement was observed in 49% of patients, most commonly in the vestibule and vestibular nerves.
  • Enhancement correlated significantly with decreased horizontal canal (HC) gain, increased interaural difference in vestibular-evoked myogenic potentials, and longer time from symptom onset to MRI.
  • The imaging demonstrated high sensitivity (92.3%) and specificity (81.5%) for predicting enhancement.

Conclusions:

  • Delayed 4-hour 3D-FLAIR MRI with gadolinium enhancement reveals abnormalities in nearly half of AUPV/VN patients.
  • MRI findings show good correlation with neurotologic evaluation results.
  • This MRI technique can help delineate affected structures in AUPV/VN, with findings potentially influenced by vestibular deficit extent, imaging timing, and etiology.