Cortical auditory dysfunction in benign rolandic epilepsy
Dana F Boatman1, William H Trescher, Cynthia Smith
1Department of Neurology, John Hopkins Hospital, Baltimore 21287, USA. dboatma@jhmi.edu
Insights
Children with benign rolandic epilepsy (BRE) show impaired speech recognition, especially in noise. This suggests nonprimary auditory cortex dysfunction, not just attention issues, highlighting the need for auditory testing in BRE patients.
Area of Science:
- Neuroscience
- Pediatrics
- Audiology
Background:
- Benign rolandic epilepsy (BRE) is a common childhood epilepsy syndrome.
- Auditory processing can be affected in neurological conditions.
- Comprehensive auditory evaluation is crucial for understanding developmental impacts.
Purpose of the Study:
- To assess cortical auditory function and speech recognition in children with BRE.
- To investigate potential links between auditory processing and EEG findings in BRE.
Main Methods:
- Compared 7 children with BRE to 7 age-matched controls.
- Utilized audiometric, behavioral, and electrophysiological (EEG, auditory-evoked potentials) testing.
- Assessed speech recognition in quiet and noisy environments.
Main Results:
- Children with BRE exhibited normal hearing in quiet but struggled with speech recognition in background noise.
- Mismatch negativity (MMN) responses to speech were abnormal in BRE patients.
- A correlation was observed between auditory impairments and centrotemporal spiking on EEG.
Conclusions:
- BRE is associated with specific speech recognition deficits, indicating nonprimary auditory cortex dysfunction.
- These auditory impairments are not solely due to attention deficits.
- Findings emphasize the importance of thorough auditory assessments in children with BRE.
Purpose:
To evaluate cortical auditory function, including speech recognition, in children with benign rolandic epilepsy (BRE).
Methods:
Fourteen children, seven patients with BRE and seven matched controls, underwent audiometric and behavioral testing, simultaneous EEG recordings, and auditory-evoked potential recordings with speech and tones. Speech recognition was tested under multiple listening conditions.
Results:
All participants demonstrated normal speech recognition abilities in quiet, as well as normal peripheral and subcortical auditory function. BRE patients performed significantly worse than controls when speech recognition was tested under adverse listening conditions, including background noise. Five BRE patients who were impaired on two or more tests had centrotemporal spiking on awake EEG. There were no significant group differences in the latency or amplitude of early N100 cortical responses to speech or tones. Conversely, the mismatch negativity, a preattentive index of cortical processing that is elicited passively, was absent or prolonged for speech, but not tones, in BRE patients as compared to controls.
Discussion:
Children with BRE demonstrated specific speech recognition impairments. Our evoked potential findings indicate that these behavioral impairments reflect dysfunction of nonprimary auditory cortex and cannot be attributed solely to attention difficulties. A possible association between auditory impairments and centrotemporal spiking (>1/min) on awake EEG was identified. The pattern of speech recognition impairments observed is a known risk factor for academic difficulties in school-age children. Our results underscore the importance of comprehensive auditory testing, using behavioral and electrophysiological measures, in children with BRE.
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