Related Experiment Video
Updated: Mar 20, 2026
Data Acquisition and Analysis In Brainstem Evoked Response Audiometry In Mice
Published on: May 10, 2019
Test-Retest Reliability of the Binaural Interaction Component of the Auditory Brainstem Response
Alexander T Ferber1, Victor Benichoux, Daniel J Tollin
11Neuroscience Program, University of Colorado Anschutz Medical Campus-School of Medicine, Aurora, Colorado, USA; 2Medical Scientist Training Program, University of Colorado Anschutz Medical Campus-School of Medicine, Aurora, Colorado, USA; 3Department of Physiology and Biophysics, University of Colorado Anschutz Medical Campus-School of Medicine, Aurora, Colorado, USA; and 4Department of Otolaryngology, University of Colorado Anschutz Medical Campus-School of Medicine, Aurora, Colorado, USA.
Objectives:
The binaural interaction component (BIC) is the residual auditory brainstem response (ABR) obtained after subtracting the sum of monaurally evoked from binaurally evoked ABRs. The DN1 peak-the first negative peak of the BIC-has been postulated to have diagnostic value as a biomarker for binaural hearing abilities. Indeed, not only do DN1 amplitudes depend systematically upon binaural cues to location (interaural time and level differences), but they are also predictive of central hearing deficits in humans. A prominent issue in using BIC measures as a diagnostic biomarker is that DN1 amplitudes not only exhibit considerable variability across subjects, but also within subjects across different measurement sessions.
Design:
In this study, the authors investigate the DN1 amplitude measurement reliability by conducting repeated measurements on different days in eight adult guinea pigs.
Results:
Despite consistent ABR thresholds, ABR and DN1 amplitudes varied between and within subjects across recording sessions. However, the study analysis reveals that DN1 amplitudes varied proportionally with parent monaural ABR amplitudes, suggesting that common experimental factors likely account for the variability in both waveforms. Despite this variability, the authors show that the shape of the dependence between DN1 amplitude and interaural time difference is preserved. The authors then provide a BIC normalization strategy using monaural ABR amplitude that reduces the variability of DN1 peak measurements. Finally, the authors evaluate this normalization strategy in the context of detecting changes of the DN1 amplitude-to-interaural time difference relationship.
Conclusions:
The study results indicate that the BIC measurement variability can be reduced by a factor of two by performing a simple and objective normalization operation. The authors discuss the potential for this normalized BIC measure as a biomarker for binaural hearing.
