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Of kittens and kids: altered cortical maturation following profound deafness and cochlear implant use
1Neuroscan Labs, El Paso, TX 79912, USA. cponton@neuroscan.com
Insights
Cochlear implants (CI) in deaf children show altered auditory brain development. Despite electrical stimulation, auditory evoked potentials (AEPs) reveal persistent immaturity, suggesting long-term effects of early deafness on the maturing central nervous system.
Area of Science:
- Neuroscience
- Auditory Neuroscience
- Developmental Neuroscience
Background:
- Profoundly deaf children using cochlear implants (CI) offer insights into auditory sensory deprivation's effects on the developing central nervous system.
- Previous studies indicated altered auditory cortical maturation in CI users, evidenced by latency delays and morphological changes in auditory evoked potentials (AEPs).
Purpose of the Study:
- To investigate the long-term effects of cochlear implantation on auditory cortical maturation in profoundly deaf children.
- To analyze changes in auditory evoked potentials (AEPs) in children with cochlear implants (CI) compared to normal-hearing (NH) peers.
Main Methods:
- Analysis of longitudinal and cross-sectional data of auditory evoked potentials (AEPs) in children with cochlear implants (CI) and age-matched normal-hearing (NH) peers.
- Comparison of scalp-recorded AEPs in implanted children with local field potentials from deaf white kittens to assess cross-species similarities.
Main Results:
- Auditory evoked potentials (AEPs) in adolescent cochlear implant (CI) users remain significantly different from normal-hearing (NH) peers, with prolonged P(1) peak latency and larger amplitude.
- The N(1b) potential, a normal component of auditory evoked potentials (AEPs), fails to emerge in most tested CI users, even after years of device use.
- Evidence suggests persistent immaturity of superficial layer axons negatively impacts N(1b) generation and overall AEP morphology in CI users.
Conclusions:
- Cochlear implantation (CI) does not fully normalize auditory cortical maturation in profoundly deaf children, with persistent alterations in auditory evoked potentials (AEPs) observed.
- A persistent immaturity of superficial layer axons is proposed as a key factor underlying abnormal AEP maturation in CI users.
- Findings in children and deaf kittens suggest that early profound deafness and subsequent cochlear implant (CI) stimulation result in lasting immaturity of cortical activation.
Abstract:
Profoundly deaf children who use a cochlear implant (CI) provide a unique opportunity to investigate the effects of auditory sensory deprivation on the maturing human central nervous system. Previous results suggest that children fitted with a CI show evidence of altered auditory cortical maturation, based on evoked potentials. This altered maturation was characterized by both latency delays and morphological changes in the cortical auditory evoked potentials (AEPs). Based on prolonged P(1) latencies compared to age-matched normal-hearing (NH) peers, these data suggested a delayed maturation nearly equivalent to the period of deafness. However, rates of maturation for this AEP peak were essentially the same in NH and CI children. This suggests that, given enough time, the AEPs of CI children would assume the characteristic morphology found in older NH teens and NH adults. However, the data also indicated a substantial alteration of the typical set of obligatory P(1)-N(1b)-P(2) peaks, specifically related to the absence of the N(1) potential. Recent analyses of more extensive sets of longitudinal and cross-sectional data indicate that even after many years of implant use, the AEPs of CI users in their late teens remain very different from those of their NH peers. The P(1) peak latency remains prolonged and P(1) amplitude remains much larger in CI users than in age-matched NH teens. These findings suggested that age-related changes in the P(1) peak are completed by 12 years of age. In addition, the normal N(1b) peak fails to emerge in virtually all of the CI children tested in our laboratory. A major new interpretation of the abnormal maturation of AEP waveforms in CI children is presented. It is based on direct evidence showing that a persistent immaturity of the superficial layer axons has persistent negative effects on the generation of the N(1b) and, consequently, on the morphology of the AEPs. A comparison of scalp-recorded AEPs from implanted children with local field potentials measured from the cortical surface in deaf white kittens suggests the effects of deafness and CI use are similar across these mammalian species. For both species, a period of profound deafness followed by CI stimulation reveals a substantial immaturity in cortical activation even after a period of electrical stimulation by the CI.