Skip to main content

Advertisement

Log in

Morphometric evaluation of facial and vestibulocochlear nerves using magnetic resonance imaging: comparison of Menière’s disease ears with normal hearing ears

  • Otology
  • Published:
European Archives of Oto-Rhino-Laryngology Aims and scope Submit manuscript

Abstract

Loss of neural structures (such as hair cells or neurones within the spiral ganglion) has been proposed to be involved in Menière’s disease (MD) (Spoendlin et al. Acta oto-laryngologica Supplementum 499:1–21, 1; Merchant et al. Eur Arch Oto-Rhino-Laryngol Off J Eur Feder Oto-Rhino-Laryngol Soc (EUFOS) Affil German Soc Oto-Rhino-Laryngol Head Neck Surg 252(2):63–75, 2; Tsuji et al. Ann Otol Rhinol Laryngol Suppl 81:26–31, 3; Kariya, Otol Neurotol Off Publ Am Otol Soc Am Neurotol Soc Eur Acad Otol Neurotol 28(8):1063–1068, 4; Megerian Laryngoscope 115(9):1525–1535, 5) but this has yet to be confirmed. Therefore, the aim of this study was to investigate morphometric changes of VIIth and VIIIth cranial nerve in MD. MD is characterized by episodic vertigo, tinnitus, fluctuating hearing loss, and aural fullness. The exact pathophysiological mechanisms involved such as viral infections, autoimmune processes, genetic predisposition, cellular apoptosis, and oxidative stress are still not clear. Using a T2-weighted 3D-GE “constructive interference in steady state” (CISS) 3T magnetic resonance imaging (MRI) sequence, we evaluated the properties of the VIIth and VIIIth cranial nerves as they passed from the cerebellopontine angle to the inner ear modiolus. 21 patients with MD were examined along with 39 normal controls. Bidirectional nerve diameters and cross-sectional areas (CSA) were measured in a transverse plane. The comparison of study and control group showed statistically significant (P < 0.000595 after Bonferroni correction) differences between the CSA measurements. The facial, cochlear, superior vestibular, and inferior vestibular nerves (FN, CN, SVN, IVN) of MD patients were significantly larger than those of the control group, both on the MD-affected side and on the healthy side. Thus for example, the cochlear nerve CSA measurements were 0.69 ± 0.14 mm2 (P < 0.0001) in the affected ears of the unilateral MD group, 0.70 ± 0.12 mm2 (P < 0.0001) in the affected ears of the cohort including the bilateral MD group, 0.71 ± 0.13 mm2 (P < 0.0001) in the non-affected ears of the MD patients, as compared to 0.46 ± 0.14 mm2 in the control group. The perpendicular nerve diameters were found to vary according to site of measurement and type of measurement used. For example a statistically significant enlargement of the short diameter measurements of the SVN at the level of the meatus was found, but not of long diameter measurements at the same site. Although cellular death would theoretically be expected to lead to a decreased nerve thickness, our data showed a swelling of cranial nerves VII and VIII within the study group compared to our normal hearing control group. The similar reaction of the facial nerve supports mediator-based theories of MD pathophysiology.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  1. Spoendlin H, Balle V, Bock G, Bredberg G, Danckwardt-Lilliestrom N, Felix H et al (1992) Multicentre evaluation of the temporal bones obtained from a patient with suspected Meniere’s disease. Acta oto-laryngologica Supplementum 499:1–21

    Article  CAS  PubMed  Google Scholar 

  2. Merchant SN, Rauch SD, Nadol JB Jr (1995) Meniere’s disease. Eur Arch Oto-Rhino-Laryngol Off J Eur Feder Oto-Rhino-Laryngol Soc (EUFOS) Affil German Soc Oto-Rhino-Laryngol Head Neck Surg 252(2):63–75

    CAS  Google Scholar 

  3. Tsuji K, Velazquez-Villasenor L, Rauch SD, Glynn RJ, Wall C 3rd, Merchant SN (2000) Temporal bone studies of the human peripheral vestibular system. Meniere’s disease. Ann Otol Rhinol Laryngol Suppl 81:26–31

    Article  Google Scholar 

  4. Kariya S, Cureoglu S, Fukushima H, Kusunoki T, Schachern PA, Nishizaki K et al (2007) Histopathologic changes of contralateral human temporal bone in unilateral Meniere’s disease. Otol Neurotol Off Publ Am Otol Soc Am Neurotol Soc Eur Acad Otol Neurotol 28(8):1063–1068

    Article  Google Scholar 

  5. Megerian CA (2005) Diameter of the cochlear nerve in endolymphatic hydrops: implications for the etiology of hearing loss in Meniere’s disease. Laryngoscope 115(9):1525–1535

    Article  PubMed  Google Scholar 

  6. Syed I, Aldren C (2012) Meniere’s disease: an evidence based approach to assessment and management. Int J Clin Pract 66(2):166–170

    Article  CAS  PubMed  Google Scholar 

  7. Semaan MT, Alagramam KN, Megerian CA (2005) The basic science of Meniere’s disease and endolymphatic hydrops. Curr Opin Otolaryngol Head Neck Surg 13(5):301–307

    Article  PubMed  Google Scholar 

  8. Gurkov R, Berman A, Dietrich O, Flatz W, Jerin C, Krause E et al (2015) MR volumetric assessment of endolymphatic hydrops. Eur Radiol 25(2):585–595

    Article  CAS  PubMed  Google Scholar 

  9. Pyykko I, Nakashima T, Yoshida T, Zou J, Naganawa S (2013) Meniere’s disease: a reappraisal supported by a variable latency of symptoms and the MRI visualisation of endolymphatic hydrops. BMJ Open 3(2):e001555

    Article  PubMed  PubMed Central  Google Scholar 

  10. Gurkov R, Flatz W, Ertl-Wagner B, Krause E (2013) Endolymphatic hydrops in the horizontal semicircular canal: a morphologic correlate for canal paresis in Meniere’s disease. Laryngoscope 123(2):503–506

    Article  PubMed  Google Scholar 

  11. Gurkov R, Flatz W, Louza J, Strupp M, Ertl-Wagner B, Krause E (2012) Herniation of the membranous labyrinth into the horizontal semicircular canal is correlated with impaired caloric response in Meniere’s disease. Otol Neurotol Off Publ Am Otol Soc Am Neurotol Soc Eur Acad Otol Neurotol 33(8):1375–1379

    Article  Google Scholar 

  12. Jaryszak EM, Patel NA, Camp M, Mancuso AA, Antonelli PJ (2009) Cochlear nerve diameter in normal hearing ears using high-resolution magnetic resonance imaging. Laryngoscope 119(10):2042–2045

    Article  PubMed  Google Scholar 

  13. Nakamichi R, Yamazaki M, Ikeda M, Isoda H, Kawai H, Sone M et al (2013) Establishing normal diameter range of the cochlear and facial nerves with 3D-CISS at 3T. Magn Reson Med Sci MRMS Off J Jpn Soc Magn Reson Med 12(4):241–247

    Google Scholar 

  14. Kang WS, Hyun SM, Lim HK, Shim BS, Cho JH, Lee KS (2012) Normative diameters and effects of aging on the cochlear and facial nerves in normal-hearing Korean ears using 3.0-tesla magnetic resonance imaging. Laryngoscope 122(5):1109–1114

    Article  PubMed  Google Scholar 

  15. Glastonbury CM, Davidson HC, Harnsberger HR, Butler J, Kertesz TR, Shelton C (2002) Imaging findings of cochlear nerve deficiency. AJNR Am J Neuroradiol 23(4):635–643

    PubMed  Google Scholar 

  16. Sheth S (2009) Branstetter BFt, Escott EJ. Appearance of normal cranial nerves on steady-state free precession MR images. Radiographics: a review publication of the Radiological Society of North America, Inc. 29(4):1045–1055

    Article  Google Scholar 

  17. Rubinstein D, Sandberg EJ, Cajade-Law AG (1996) Anatomy of the facial and vestibulocochlear nerves in the internal auditory canal. AJNR Am J Neuroradiol 17(6):1099–1105

    CAS  PubMed  Google Scholar 

  18. Guclu B, Sindou M, Meyronet D, Streichenberger N, Simon E, Mertens P (2012) Anatomical study of the central myelin portion and transitional zone of the vestibulocochlear nerve. Acta Neurochirurgica 154(12):2277–2283 (discussion 83)

    Article  PubMed  Google Scholar 

  19. Giesemann AM, Raab P, Lyutenski S, Dettmer S, Bultmann E, Fromke C et al (2014) Improved imaging of cochlear nerve hypoplasia using a 3-Tesla variable flip-angle turbo spin-echo sequence and a 7-cm surface coil. Laryngoscope 124(3):751–754

    Article  PubMed  Google Scholar 

  20. Gurkov R, Kantner C, Strupp M, Flatz W, Krause E, Ertl-Wagner B (2014) Endolymphatic hydrops in patients with vestibular migraine and auditory symptoms. Eur Arch Oto-Rhino-Laryngol Off J Eur Feder Oto-Rhino-Laryngol Soc (EUFOS) Affil German Soc Oto-Rhino-Laryngol Head Neck Surg 271(10):2661–2667

    Google Scholar 

  21. Gurkov R, Pyyko I, Zou J, Kentala E (2016) What is Meniere’s disease? A contemporary re-evaluation of endolymphatic hydrops. J Neurol 263(Suppl 1):S71–S81

    Article  PubMed  Google Scholar 

  22. Nakashima T, Pyykko I, Arroll MA, Casselbrant ML, Foster CA, Manzoor NF et al (2016) Meniere’s disease. Nature Rev Dis Primer 2:16028

    Article  Google Scholar 

  23. Jerin C, Krause E, Ertl-Wagner B, Gurkov R (2014) Longitudinal assessment of endolymphatic hydrops with contrast-enhanced magnetic resonance imaging of the labyrinth. Otol Neurotol Off Publ Am Otol Soc Am Neurotol Soc Eur Acad Otol Neurotol 35(5):880–883

    Article  Google Scholar 

  24. Gurkov R, Flatz W, Louza J, Strupp M, Ertl-Wagner B, Krause E (2012) In vivo visualized endolymphatic hydrops and inner ear functions in patients with electrocochleographically confirmed Meniere’s disease. Otol Neurotol Off Publ Am Otol Soc Am Neurotol Soc Eur Acad Otol Neurotol 33(6):1040–1045

    Google Scholar 

  25. Arbusow V, Derfuss T, Held K, Himmelein S, Strupp M, Gurkov R et al (2010) Latency of herpes simplex virus type-1 in human geniculate and vestibular ganglia is associated with infiltration of CD8+ T cells. J Med Virol 82(11):1917–1920

    Article  PubMed  Google Scholar 

  26. Greco A, Gallo A, Fusconi M, Marinelli C, Macri GF, de Vincentiis M (2012) Meniere’s disease might be an autoimmune condition? Autoimmun Rev 11(10):731–738

    Article  CAS  PubMed  Google Scholar 

  27. Klockars T, Kentala E (2007) Inheritance of Meniere’s disease in the finnish population. Arch Otolaryngol Head Neck Surg 133(1):73–77

    Article  PubMed  Google Scholar 

  28. Ozdogmus O, Sezen O, Kubilay U, Saka E, Duman U, San T et al (2004) Connections between the facial, vestibular and cochlear nerve bundles within the internal auditory canal. J Anat 205(1):65–75

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We thank Dr. Rebecca Maxwell for the thorough proof-reading of the manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Wilhelm Flatz.

Ethics declarations

Funding

Robert Gürkov’s institution received funding from BMBF (German Ministry of Research and Education) Grant No. 01 EO 0901.

Conflict of interest

Annika Henneberger declares that she has no conflict of interest. Birgit Ertl-Wagner declares that she has no conflict of interest. Maximilian Reiser declares that he has no conflict of interest. Robert Gürkov received research Grant/payment from Otonomy Inc. Wilhelm Flatz declares that he has no conflict of interest.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Institutional review board of University of Munich/LMU Munich, Protocol No. 093-09.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Henneberger, A., Ertl-Wagner, B., Reiser, M. et al. Morphometric evaluation of facial and vestibulocochlear nerves using magnetic resonance imaging: comparison of Menière’s disease ears with normal hearing ears. Eur Arch Otorhinolaryngol 274, 3029–3039 (2017). https://doi.org/10.1007/s00405-017-4616-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00405-017-4616-6

Keywords

Navigation