Department of Speech, Language, and Hearing Sciences, Purdue University, West Lafayette, IN; Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN.
Department of Speech, Language, and Hearing Sciences, Purdue University, West Lafayette, IN.
Neuroscience. 2019 May 21;407:53-66. doi: 10.1016/j.neuroscience.2019.02.031. Epub 2019 Mar 8.
Studies in multiple species, including in post-mortem human tissue, have shown that normal aging and/or acoustic overexposure can lead to a significant loss of afferent synapses innervating the cochlea. Hypothetically, this cochlear synaptopathy can lead to perceptual deficits in challenging environments and can contribute to central neural effects such as tinnitus. However, because cochlear synaptopathy can occur without any measurable changes in audiometric thresholds, synaptopathy can remain hidden from standard clinical diagnostics. To understand the perceptual sequelae of synaptopathy and to evaluate the efficacy of emerging therapies, sensitive and specific non-invasive measures at the individual patient level need to be established. Pioneering experiments in specific mice strains have helped identify many candidate assays. These include auditory brainstem responses, the middle-ear muscle reflex, envelope-following responses, and extended high-frequency audiograms. Unfortunately, because these non-invasive measures can be also affected by extraneous factors other than synaptopathy, their application and interpretation in humans is not straightforward. Here, we systematically examine six extraneous factors through a series of interrelated human experiments aimed at understanding their effects. Using strategies that may help mitigate the effects of such extraneous factors, we then show that these suprathreshold physiological assays exhibit across-individual correlations with each other indicative of contributions from a common physiological source consistent with cochlear synaptopathy. Finally, we discuss the application of these assays to two key outstanding questions, and discuss some barriers that still remain. This article is part of a Special Issue entitled: Hearing Loss, Tinnitus, Hyperacusis, Central Gain.
在多种物种(包括死后的人类组织)中的研究表明,正常衰老和/或过度声暴露可导致支配耳蜗的传入性突触大量丧失。理论上,这种耳蜗突触病可导致在挑战性环境中的感知缺陷,并可导致耳鸣等中枢神经效应。然而,由于耳蜗突触病可在听阈无任何可测量的变化的情况下发生,因此突触病可能隐藏在标准临床诊断之外。为了了解突触病的感知后果,并评估新兴疗法的疗效,需要在个体患者层面建立敏感和特异的非侵入性测量方法。在特定的小鼠品系中进行的开创性实验有助于确定许多候选测定方法。这些方法包括听觉脑干反应、中耳肌反射、包络跟随反应和扩展高频听力图。不幸的是,由于这些非侵入性测量方法也可能受到除突触病以外的其他外来因素的影响,因此它们在人类中的应用和解释并不简单。在这里,我们通过一系列相互关联的人类实验系统地检查了六个外来因素,旨在了解它们的影响。我们使用可能有助于减轻这些外来因素影响的策略,然后表明这些阈上生理测定方法彼此之间存在相关性,表明它们来自与耳蜗突触病一致的共同生理来源。最后,我们讨论了这些测定方法在两个关键的悬而未决的问题中的应用,并讨论了一些仍然存在的障碍。本文是一个特刊的一部分,主题是:听力损失、耳鸣、听觉过敏、中枢增益。