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年龄相关性听力损失会加速快速言语理解能力的下降以及皮质网络连接的失代偿。

Age-related hearing loss accelerates the decline in fast speech comprehension and the decompensation of cortical network connections.

作者信息

Huang He-Mei, Chen Gui-Sheng, Liu Zhong-Yi, Meng Qing-Lin, Li Jia-Hong, Dong Han-Wen, Chen Yu-Chen, Zhao Fei, Tang Xiao-Wu, Gao Jin-Liang, Chen Xi-Ming, Cai Yue-Xin, Zheng Yi-Qing

机构信息

Department of Otolaryngology, Sun Yat-sen Memorial Hospital; Institute of Hearing and Speech-Language Science, Sun Yat-sen University, Guangzhou, Guangdong Province, China.

Department of Otolaryngology, Sun Yat-sen Memorial Hospital; Institute of Hearing and Speech-Language Science, Sun Yat-sen University, Guangzhou; Department of Otolaryngology, Shenzhen-Shanwei Central Hospital, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Shanwei, Guangdong Province, China.

出版信息

Neural Regen Res. 2023 Sep;18(9):1968-1975. doi: 10.4103/1673-5374.361530.

Abstract

Patients with age-related hearing loss face hearing difficulties in daily life. The causes of age-related hearing loss are complex and include changes in peripheral hearing, central processing, and cognitive-related abilities. Furthermore, the factors by which aging relates to hearing loss via changes in auditory processing ability are still unclear. In this cross-sectional study, we evaluated 27 older adults (over 60 years old) with age-related hearing loss, 21 older adults (over 60 years old) with normal hearing, and 30 younger subjects (18-30 years old) with normal hearing. We used the outcome of the upper-threshold test, including the time-compressed threshold and the speech recognition threshold in noisy conditions, as a behavioral indicator of auditory processing ability. We also used electroencephalography to identify presbycusis-related abnormalities in the brain while the participants were in a spontaneous resting state. The time-compressed threshold and speech recognition threshold data indicated significant differences among the groups. In patients with age-related hearing loss, information masking (babble noise) had a greater effect than energy masking (speech-shaped noise) on processing difficulties. In terms of resting-state electroencephalography signals, we observed enhanced frontal lobe (Brodmann's area, BA11) activation in the older adults with normal hearing compared with the younger participants with normal hearing, and greater activation in the parietal (BA7) and occipital (BA19) lobes in the individuals with age-related hearing loss compared with the younger adults. Our functional connection analysis suggested that compared with younger people, the older adults with normal hearing exhibited enhanced connections among networks, including the default mode network, sensorimotor network, cingulo-opercular network, occipital network, and frontoparietal network. These results suggest that both normal aging and the development of age-related hearing loss have a negative effect on advanced auditory processing capabilities and that hearing loss accelerates the decline in speech comprehension, especially in speech competition situations. Older adults with normal hearing may have increased compensatory attentional resource recruitment represented by the top-down active listening mechanism, while those with age-related hearing loss exhibit decompensation of network connections involving multisensory integration.

摘要

患有年龄相关性听力损失的患者在日常生活中面临听力困难。年龄相关性听力损失的病因复杂,包括外周听力、中枢处理和认知相关能力的变化。此外,衰老通过听觉处理能力变化与听力损失相关的因素仍不清楚。在这项横断面研究中,我们评估了27名年龄在60岁以上患有年龄相关性听力损失的老年人、21名年龄在60岁以上听力正常的老年人以及30名年龄在18至30岁听力正常的年轻人。我们将上阈值测试的结果,包括时间压缩阈值和嘈杂环境下的言语识别阈值,作为听觉处理能力的行为指标。我们还使用脑电图来识别参与者在自发静息状态下与老年性聋相关的大脑异常。时间压缩阈值和言语识别阈值数据表明各组之间存在显著差异。在患有年龄相关性听力损失的患者中,信息掩蔽(嘈杂噪声)比能量掩蔽(言语形状噪声)对处理困难的影响更大。就静息状态脑电图信号而言,我们观察到与听力正常的年轻参与者相比,听力正常的老年人额叶(布罗德曼区,BA11)激活增强,与年轻成年人相比,患有年龄相关性听力损失的个体顶叶(BA7)和枕叶(BA19)激活更强。我们的功能连接分析表明,与年轻人相比,听力正常的老年人在包括默认模式网络、感觉运动网络、扣带回-脑岛网络、枕叶网络和额顶网络在内的网络之间表现出增强的连接。这些结果表明,正常衰老和年龄相关性听力损失的发展都会对高级听觉处理能力产生负面影响,并且听力损失会加速言语理解能力的下降,尤其是在言语竞争情境中。听力正常的老年人可能通过自上而下的主动倾听机制增加补偿性注意力资源的募集,而患有年龄相关性听力损失的老年人则表现出涉及多感官整合的网络连接失代偿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a820/10233765/115f76757885/NRR-18-1968-g002.jpg

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