隐性听力损失:目前的观点和潜在的治疗方法

Diyan Chen, Gaogan Jia, Yusu Ni, Yan Chen
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引用次数: 3

摘要

隐蔽性听力损失(HHL)是近年来备受关注的一种听觉功能障碍,其特征是听力阈值正常或接近正常的言语歧视和理解障碍。HHL的病理机制复杂,尚未完全了解。HHL可由听觉皮层等中枢神经系统疾病和/或内耳病理改变引起。到目前为止,两种病理现象,突触病和听神经脱髓鞘,已被报道为耳源性HHL的潜在原因。本文就HHL的临床、生理特点及耳源性HHL的分子病理机制进行综述,以期为今后临床应用提供潜在的治疗靶点。关键词:听觉;耳蜗毛细胞;髓鞘脱失;听力损失;隐性听力损失;雪旺细胞;螺旋神经节神经元;突触;synaptopathy
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hidden hearing loss: current perspectives and potential therapies
Hidden hearing loss (HHL), an auditory dysfunction that has gained much recent attention, has the hallmarks of speech discrimination and intelligibility deficits with normal or near-normal hearing thresholds. The pathological mechanisms of HHL are complicated and are not yet fully understood. HHL can be resulted from disorders of the central nervous system such as auditory cortex, and/or pathological changes of inner ear. Thus far, 2 pathological phenomena, synaptopathy and auditory nerve demyelination, have been reported as underlying causes of otogenic HHL. Here, we review the clinical and physiological characteristics of HHL as well as the molecular pathological mechanisms of otogenic HHL and aim to allude to potential therapy targets for clinical applications in the future. Key words: auditory; cochlear hair cells; demyelination; hearing loss; hidden hearing loss; Schwann cells; spiral ganglion neurons; synapse; synaptopathy
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