Time course of visual plasticity following adult-onset deafness

When deprived of a sensory modality, the brain often compensates with supranormal performance in other intact systems. While this compensatory plasticity is typically attributed to early sensory loss, plasticity following adult-onset sensory loss remains poorly understood despite its clinical relevance. In many patients, adult-onset hearing loss precedes treatment by cochlear implantation, yet little is known about the neural changes occurring before this intervention. The present study examines this transitional stage using a well-established adult cat model to examine visual plasticity after hearing loss in adulthood. We employed motion-onset visually evoked potentials (VEPs), a technique validated in our previous studies, to examine compensatory neural changes over time. VEPs are widely used in human neurophysiology and offer a translational bridge between basic science and clinical research. Over a 400-day period post adult-onset deafness, we observed gradual amplification in VEP signal power and P1 amplitude, alongside shortened peak latency. Our findings provide evidence that adult-onset deafness can induce compensatory visual plasticity and highlights VEPs as a promising biomarker for tracking such changes. This exploratory study establishes a platform for future research examining post-deafness intervention, such as cochlear implantation.

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Publication Details

Journal
Scientific Reports
Published
2026-02-17
DOI
https://doi.org/10.1038/s41598-026-39490-8
Primary Topic
Hearing, Cochlea, Tinnitus, Genetics
Type
article
Field-Weighted Citation Impact
0.00

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article

Time course of visual plasticity following adult-onset deafness

Siyu Zhu, Stephen G. Lomber, Xiaohan Bao
Scientific Reports
Hearing, Cochlea, Tinnitus, Genetics
article

Time course of visual plasticity following adult-onset deafness

Siyu Zhu, Stephen G. Lomber, Xiaohan Bao
article en

Abstract

When deprived of a sensory modality, the brain often compensates with supranormal performance in other intact systems. While this compensatory plasticity is typically attributed to early sensory loss, plasticity following adult-onset sensory loss remains poorly understood despite its clinical relevance. In many patients, adult-onset hearing loss precedes treatment by cochlear implantation, yet little is known about the neural changes occurring before this intervention. The present study examines this transitional stage using a well-established adult cat model to examine visual plasticity after hearing loss in adulthood. We employed motion-onset visually evoked potentials (VEPs), a technique validated in our previous studies, to examine compensatory neural changes over time. VEPs are widely used in human neurophysiology and offer a translational bridge between basic science and clinical research. Over a 400-day period post adult-onset deafness, we observed gradual amplification in VEP signal power and P1 amplitude, alongside shortened peak latency. Our findings provide evidence that adult-onset deafness can induce compensatory visual plasticity and highlights VEPs as a promising biomarker for tracking such changes. This exploratory study establishes a platform for future research examining post-deafness intervention, such as cochlear implantation.

Scientific ReportsVol. 16(1)
The University of Texas at Arlington (US), McGill University (CA)
Canadian Institutes of Health Research
Openalex Percentile: Top 51%
Hearing, Cochlea, Tinnitus, Genetics
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