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与年龄相关的听觉神经缺陷在整个听觉系统中传播中枢增益:与皮质微结构和言语识别的关联。

Age-related auditory nerve deficits propagate central gain throughout the auditory system: Associations with cortical microstructure and speech recognition.

作者信息

Fabrizio-Stover Emily M, Dias James W, McClaskey Carolyn M, Harris Kelly C

机构信息

Medical University of South Carolina, Department of Otolaryngology - Head and Neck Surgery.

出版信息

bioRxiv. 2025 May 21:2025.05.19.654964. doi: 10.1101/2025.05.19.654964.

DOI:10.1101/2025.05.19.654964
PMID:40475667
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12139991/
Abstract

There is growing evidence that many perceptual difficulties associated with age-related hearing loss are not solely due to cochlear damage and are exacerbated by changes within the central nervous system. We examined electrophysiological (EEG) responses to clicks and diffusion kurtosis imaging (DKI) in 49 older (29 female) and 26 younger (20 female) adults to determine the extent to which auditory nerve (AN) deficits in older adults contributed to functional and structural changes throughout the auditory system. Older adults exhibited smaller AN responses, similar brainstem responses, and larger auditory cortex (AC) responses, demonstrating progressive "central gain". Audiometric thresholds were not predictive of EEG measures. Reduced AN function predicted deficits in cortical microstructure (lower AC fractional anisotropy, FA) in older adults, consistent with myelin degeneration. These lower FA values in the AC of older adults also predicted larger AC responses and more central gain. Older adults exhibited significantly lower AC FA and higher mean diffusivity (MD) than younger adults, and AC FA and MD were significant predictors of speech-in-noise (SIN) recognition in older adults. The results suggest that reduced afferent input in older adults not only results in functional changes throughout the auditory system consistent with progressive gain, but also contributes to deficits in AC structure beyond those explained by age alone, contributing to SIN deficits. Understanding the complex effects of age, reduced AN input, central gain, and AC structure on SIN recognition may provide potential therapeutic targets for intervention.

摘要

越来越多的证据表明,许多与年龄相关的听力损失相关的感知困难并非仅仅由于耳蜗损伤,还会因中枢神经系统内的变化而加剧。我们对49名老年人(29名女性)和26名年轻人(20名女性)进行了点击声的电生理(脑电图,EEG)反应和扩散峰度成像(DKI)检查,以确定老年人听觉神经(AN)缺陷在多大程度上导致了整个听觉系统的功能和结构变化。老年人表现出较小的AN反应、相似的脑干反应和较大的听觉皮层(AC)反应,表明存在渐进性的“中枢增益”。听力阈值不能预测EEG测量结果。老年人中AN功能降低预示着皮质微结构存在缺陷(AC分数各向异性,FA较低),这与髓鞘变性一致。老年人AC中这些较低的FA值还预示着AC反应更大和中枢增益更多。老年人的AC FA显著低于年轻人,平均扩散率(MD)则显著高于年轻人,并且AC FA和MD是老年人噪声中言语(SIN)识别的重要预测指标。结果表明,老年人传入输入减少不仅导致整个听觉系统出现与渐进性增益一致的功能变化,还会导致AC结构缺陷,这种缺陷超出了仅由年龄所解释的范围,进而导致SIN缺陷。了解年龄、AN输入减少、中枢增益和AC结构对SIN识别的复杂影响可能为干预提供潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/dd8995ce9394/nihpp-2025.05.19.654964v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/c3ba0724e3d5/nihpp-2025.05.19.654964v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/154b11ab385c/nihpp-2025.05.19.654964v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/52004ac777a2/nihpp-2025.05.19.654964v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/cc8da966d3ea/nihpp-2025.05.19.654964v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/65c4f6b28733/nihpp-2025.05.19.654964v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/59a5c74ee95a/nihpp-2025.05.19.654964v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/dd8995ce9394/nihpp-2025.05.19.654964v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/c3ba0724e3d5/nihpp-2025.05.19.654964v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/154b11ab385c/nihpp-2025.05.19.654964v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/52004ac777a2/nihpp-2025.05.19.654964v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/cc8da966d3ea/nihpp-2025.05.19.654964v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/65c4f6b28733/nihpp-2025.05.19.654964v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/59a5c74ee95a/nihpp-2025.05.19.654964v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/12139991/dd8995ce9394/nihpp-2025.05.19.654964v1-f0007.jpg

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本文引用的文献

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