Cochlear microphonic potential recorded by transtympanic electrocochleography in normally-hearing and

R Santarelli1, P Scimemi, E Dal Monte

  • 1Department of Medical and Surgical Specialities, Audiology and Phoniatric Service, University of Padua, Italy. rosamaria.santarelli@unipd.it

Insights

Cochlear microphonic detection is not unique to auditory neuropathy. Central nervous system pathology can enhance cochlear microphonic amplitude and duration, while auditory neuropathy patients show distinct patterns.

Area of Science:

  • Auditory Neuroscience
  • Otoacoustic Emissions
  • Electrophysiology

Background:

  • The cochlear microphonic (CM) is a receptor potential primarily generated by outer hair cells.
  • CM detection is often considered indicative of outer hair cell integrity in auditory neuropathy.

Purpose of the Study:

  • To analyze cochlear microphonic recordings in subjects with normal hearing, hearing impairment, and auditory neuropathy.
  • To investigate the influence of central nervous system (CNS) pathology on CM characteristics.

Main Methods:

  • Transtympanic electrocochleography was used to record CM in response to clicks.
  • 502 subjects with normal hearing or hearing impairment and 20 patients with auditory neuropathy were analyzed.
  • Recordings were categorized based on the presence or absence of CNS pathology (CNS+ and CNS-).

Main Results:

  • CM amplitude decreased with increasing compound action potential (CAP) threshold but was detectable even in profound hearing loss.
  • CM amplitude was significantly higher in CNS+ subjects compared to CNS- subjects with normal hearing and at a 70 dB nHL CAP threshold.
  • CM duration was significantly longer in auditory neuropathy and CNS+ patients compared to CNS- subjects.
  • Auditory neuropathy patients exhibited CM with amplitudes and thresholds similar to normally-hearing CNS- subjects.

Conclusions:

  • Cochlear microphonic detection is not a unique diagnostic marker for auditory neuropathy.
  • Central nervous system pathology may enhance CM amplitude and duration, potentially due to efferent system dysfunction.
  • Auditory neuropathy is associated with long-lasting, high-frequency CM, possibly resulting from afferent pathway lesions, efferent dysfacilitation, and outer hair cell loss.