Auditory and vestibular function in mitochondrial patients harbouring the m.3243A>G variant.

IF 4.1 Q1 CLINICAL NEUROLOGY Brain communications Pub Date : 2024-10-14 eCollection Date: 2024-01-01 DOI:10.1093/braincomms/fcae361
Renae J Stefanetti, Jane Newman, Alasdair P Blain, Donella Chisari, Gráinne S Gorman, Gary Rance
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Abstract

Hearing impairment is a frequent clinical feature in patients with mitochondrial disease harbouring the pathogenic variant, m.3243A>G. However, auditory neural dysfunction, its perceptual consequences and implications for patient management are not established. Similarly, the association with vestibular impairment has not yet been explored. This case-control study investigated in 12 adults with genetically confirmed m.3243A>G adults [9 females; 45.5 ± 16.3 years (range 18-66); 47.1 ± 21.5 hearing level, dB] compared with 12 age, sex and hearing level-matched controls with sensory (cochlear level) hearing loss [9 females; 46.6 ± 11.8 years (range 23-59); 47.7 ± 25.4 hearing level, dB]. Participants underwent a battery of electroacoustic, electrophysiologic and perceptual tests, which included pure tone audiometry, otoacoustic emissions, auditory brainstem responses, auditory temporal processing measures, monaural/binaural speech perception, balance and vestibular testing and self-reported questionnaires (dizziness and hearing disability). Our findings showed evidence of auditory neural abnormality and perceptual deficits greater than expected for cochlear pathology. Compared with matched controls with sensory hearing loss, adults with mitochondrial disease harbouring m.3243A>G had abnormal electrophysiologic responses from the VIII nerve and auditory brainstem (P = 0.005), an impaired capacity to encode rapidly occurring acoustic signal changes (P = 0.005), a reduced ability to localize sound sources (P = 0.028) and impaired speech perception in background noise (P = 0.008). Additionally, vestibular dysfunction (P = 0.011), greater perceived dizziness (P = 0.001) and reduced stance time (balance, P = 0.009) were also seen in participants with m.3243A>G mitochondrial disease when compared with matched counterparts. This pilot study revealed that auditory evaluation including evoked potential responses from the auditory nerve/brainstem and speech perception in noise tests should form an important part of the management for individuals with m.3243A>G-related mitochondrial disease. Those presenting with hearing impairment and symptoms concerning balance and dizziness should undergo vestibular testing and appropriate management.

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携带 m.3243A>G 变异基因的线粒体患者的听觉和前庭功能。
听力障碍是携带致病变异体 m.3243A>G 的线粒体疾病患者经常出现的临床特征。然而,听觉神经功能障碍、其感知后果以及对患者管理的影响尚未确定。同样,与前庭功能障碍的关系也尚未得到探讨。这项病例对照研究调查了 12 名经基因证实患有 m.3243A>G 的成人(9 名女性;45.5 ± 16.3 岁(18-66 岁);47.1 ± 21.5 听力水平,dB)与 12 名年龄、性别和听力水平匹配的感觉性(耳蜗水平)听力损失对照组(9 名女性;46.6 ± 11.8 岁(23-59 岁);47.7 ± 25.4 听力水平,dB)。参与者接受了一系列电声、电生理和感知测试,包括纯音测听、耳声发射、听觉脑干反应、听觉时间处理测量、单耳/双耳言语感知、平衡和前庭测试以及自我报告问卷(头晕和听力残疾)。我们的研究结果表明,听觉神经异常和知觉缺陷的程度超出了耳蜗病变的预期。与感觉性听力损失的匹配对照组相比,携带 m.3243A>G 的线粒体疾病成人患者的第八神经和听觉脑干的电生理反应异常(P = 0.005),对快速发生的声音信号变化的编码能力受损(P = 0.005),声源定位能力下降(P = 0.028),在背景噪声中的言语感知能力受损(P = 0.008)。此外,与匹配的同行相比,m.3243A>G 线粒体疾病患者还存在前庭功能障碍(P = 0.011)、眩晕感更强(P = 0.001)和站立时间缩短(平衡,P = 0.009)。这项试验研究表明,听觉评估(包括听神经/脑干的诱发电位反应和噪音中的言语感知测试)应成为 m.3243A>G 相关线粒体疾病患者管理的重要组成部分。听力受损并伴有平衡和头晕症状的患者应接受前庭测试和适当的治疗。
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