Fachartikel

Radiological feature heterogeneity supports etiological diversity among patient groups in Meniere’s disease

We aimed to determine the prevalence of radiological temporal bone features that in previous studies showed only a weak or an inconsistent association with the clinical diagnosis of Meniere’s disease (MD), in two groups of MD patients (n = 71) with previously established distinct endolymphatic sac pathologies; i.e. the group MD-dg (ES degeneration) and the group MD-hp (ES hypoplasia). Delayed gadolinium-enhanced MRI and high-resolution CT data were used to determine and compare between and within (affected vs. non-affected side) groups geometric temporal bone features (lengths, widths, contours), air cell tract volume, height of the jugular bulb, sigmoid sinus width, and MRI signal intensity alterations of the ES. Temporal bone features with significant intergroup differences were the retrolabyrinthine bone thickness (1.04 +/- 0.69 mm, MD-hp; 3.1 +/- 1.9 mm, MD-dg; p < 0.0001); posterior contour tortuosity (mean arch-to-chord ratio 1.019 +/- 0.013, MD-hp; 1.096 +/- 0.038, MD-dg; p < 0.0001); and the pneumatized volume (1.37 [0.86] cm(3), MD-hp; 5.25 [3.45] cm(3), MD-dg; p = 0.03). Features with differences between the affected and non-affected sides within the MD-dg group were the sigmoid sinus width (6.5 +/- 1.7 mm, affected; 7.6 +/- 2.1 mm, non-affected; p = 0.04) and the MRI signal intensity of the endolymphatic sac (median signal intensity, affected vs. unaffected side, 0.59 [IQR 0.31-0.89]). Radiological temporal bone features known to be only weakly or inconsistently associated with the clinical diagnosis MD, are highly prevalent in either of two MD patient groups. These results support the existence of diverse-developmental and degenerative-disease etiologies manifesting with distinct radiological temporal bone abnormalities.

Download Article

The .pdf version of this article is for internal use only. Do not proceed unless you have the necessary rights.

Proceed Cancel

Reference

D. Bachinger, N. Filidoro, M. Naville, N. Juchler, V. Kurtcuoglu, J. B. Nadol, Jr., B. Schuknecht, T. Kleinjung, D. Veraguth, A. H. Eckhard. Scientific Reports, 13(1), 10303 (2023). doi: 10.1038/s41598-023-36479-5