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Updated: Jan 15, 2026

In Vivo Morphometric Analysis of Human Cranial Nerves Using Magnetic Resonance Imaging in Menière's Disease Ears and Normal Hearing Ears
Published on: February 21, 2018
Changes in the Neurovascular Unit in Meniere's Disease
Steven D Curry1,2, Ivan A Lopez2, Gail Ishiyama2,3
1House Clinic.
Hypothesis:
Degenerative changes in the neurovascular unit (NVU) in the human spiral ganglia (SG) in patients with Meniere's disease (MD) compared with normal patients underlie the clinical manifestations of MD.
Background:
Endolymphatic hydrops (EH) is the pathologic correlate of MD, yet the etiology of MD is poorly understood. EH alone does not adequately explain the changes in permeability of the cochlear blood-labyrinthine barrier seen with delayed contrast MRI or fluctuations in symptoms.
Methods:
Hematoxylin and eosin sections of the cochlea were obtained from temporal bones of normal patients (n=5, age: 47 to 63 y, 1 male/4 female) and patients diagnosed with MD (n=8, age 51 to 88, 4 male/4 female). The number of spiral ganglia neurons (SGNs) in each cochlea was estimated. SGNs and blood vessels in the cochlea from normal and MD patients (archival celloidin sections from the same patients) were reliably identified with antibodies against acetylated-3-tubulin and glucose transporter-1, respectively, and visualized by immunofluorescence and laser confocal microscopy.
Results:
There was a significant decrease (50% loss) of SGNs among patients diagnosed with MD compared with age-matched controls ( P <0.05) and contralateral unaffected cochlea (35% decrease). Immunofluorescence-stained sections showed a marked decrease of blood vessels and a corresponding loss of SGNs in MD cochlea compared with controls.
Conclusions:
The decrease of spiral ganglia neurons and associated blood vessels showed regional damage of the cochlea. These results suggest that the NVU interaction may be critical to preserve the SGNs in MD and establish a framework for understanding the etiology and treatment of MD beyond EH.
Level Of Evidence:
Not applicable.
Insights
Meniere's disease involves significant loss of spiral ganglia neurons and blood vessels in the cochlea. These neurovascular unit changes suggest a new framework for understanding and treating this inner ear disorder.
Area of Science:
- Neuroscience
- Otolaryngology
- Pathology
Background:
- Meniere's disease (MD) is characterized by endolymphatic hydrops (EH), but its underlying causes remain unclear.
- EH alone does not fully explain cochlear blood-labyrinthine barrier permeability changes or symptom fluctuations observed in MD patients.
Purpose of the Study:
- To investigate degenerative changes in the neurovascular unit (NVU) of the human spiral ganglia (SG) in Meniere's disease (MD) patients.
- To compare the NVU in MD patients with that of normal individuals to understand the basis of MD's clinical manifestations.
Main Methods:
- Hematoxylin and eosin staining of cochlear sections from normal (n=5) and MD (n=8) temporal bones.
- Immunofluorescence and laser confocal microscopy using antibodies for acetylated-3-tubulin (SGNs) and glucose transporter-1 (blood vessels).
Main Results:
- A significant 50% decrease in spiral ganglia neurons (SGNs) was observed in MD patients compared to controls (P <0.05).
- A 35% decrease in SGNs was also noted in the contralateral unaffected cochlea of MD patients.
- Immunofluorescence revealed a marked reduction in blood vessels and a corresponding loss of SGNs in the cochlea of MD patients.
Conclusions:
- The observed decrease in SGNs and associated blood vessels indicates regional cochlear damage in MD.
- These findings suggest that neurovascular unit (NVU) integrity is critical for preserving SGNs in MD.
- This study provides a framework for understanding MD etiology and treatment beyond EH, focusing on NVU interactions.
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