Speech-Evoked Cortical Auditory Potentials as Biomarkers of Auditory Maturation in Children with Cochlear Implants

Zeynel Abidin Karatas1, Cengiz Durucu2

  • 1Department of Otorhinolaryngology, Duztepe Yasam Hospital, Gaziantep 27300, Turkey.

PubMed

Insights

Pediatric cochlear implant (CI) users show delayed auditory cortical maturation compared to normal-hearing peers, but P1 latency shortens with longer implant use, indicating plasticity. Speech-evoked cortical auditory evoked potentials (CAEPs) effectively measure this development.

Area of Science:

  • Neuroscience
  • Audiology
  • Developmental Pediatrics

Background:

  • Auditory cortical maturation is crucial for speech perception development in children.
  • Cochlear implants (CIs) aim to restore hearing, but auditory system development may differ.
  • Cortical auditory evoked potentials (CAEPs) offer objective measures of auditory processing.

Purpose of the Study:

  • To evaluate auditory cortical maturation in pediatric cochlear implant (CI) users.
  • To compare P1 latency in CI users with age-matched normal-hearing (NH) peers.
  • To examine the relationship between P1 latency, age, and CI duration for cortical plasticity.

Main Methods:

  • Seventy children (40 CI users, 30 NH controls) underwent CAEP recordings.
  • Speech tokens (/m/, /g/, /t/) were presented in a free-field setup.
  • P1 latency was analyzed using t-tests and Pearson correlations (p < 0.05).

Main Results:

  • CI users exhibited significantly longer P1 latencies for /m/ and /t/ stimuli compared to NH peers.
  • In NH children, P1 latency negatively correlated with age, indicating maturation.
  • In CI users, longer implant use duration correlated with shorter P1 latencies for all speech tokens.

Conclusions:

  • Speech-evoked CAEPs are sensitive, objective measures of auditory cortical development in pediatric CI users.
  • P1 latency reflects chronological and hearing-age-related maturation.
  • P1 latency serves as a biomarker for cortical plasticity and rehabilitation progress in pediatric CI care.