Stefanetti Renae J, Newman Jane, Blain Alasdair P, Chisari Donella, Gorman Gráinne S, Rance Gary
Faculty of Medical Sciences, Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.
National Institute for Health and Care Research Newcastle Biomedical Research Centre, The Medical School, Newcastle upon Tyne, NE2 4HH, UK.
Brain Commun. 2024 Oct 14;6(6):fcae361. doi: 10.1093/braincomms/fcae361. eCollection 2024.
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 ( = 0.005), an impaired capacity to encode rapidly occurring acoustic signal changes ( = 0.005), a reduced ability to localize sound sources ( = 0.028) and impaired speech perception in background noise ( = 0.008). Additionally, vestibular dysfunction ( = 0.011), greater perceived dizziness ( = 0.001) and reduced stance time (balance, = 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.
听力障碍是携带致病性变异m.3243A>G的线粒体疾病患者常见的临床特征。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明确。同样,与前庭功能障碍的关联也尚未得到探索。这项病例对照研究对12名经基因确诊携带m.3243A>G的成年人[9名女性;45.5±16.3岁(范围18 - 66岁);听力水平47.1±21.5分贝]进行了调查,并与12名年龄、性别和听力水平匹配的感音性(耳蜗水平)听力损失对照者[9名女性;46.6±11.8岁(范围23 - 59岁);听力水平47.7±25.4分贝]进行比较。参与者接受了一系列电声学、电生理学和感知测试,包括纯音听力测定、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)。我们的研究结果显示存在听觉神经异常和感知缺陷,其程度超过了耳蜗病变预期。与匹配的感音性听力损失对照者相比,携带m.3243A>G的线粒体疾病成年人的第八对脑神经和听觉脑干的电生理反应异常(P = 0.005),编码快速出现的声学信号变化的能力受损(P = 0.005),定位声源的能力降低(P = 0.028),以及在背景噪声中的言语感知受损(P = 0.008)。此外,与匹配的对照者相比,携带m.3243A>G线粒体疾病的参与者还出现前庭功能障碍(P = 0.011)、更强烈的头晕感(P = 0.001)和站立时间缩短(平衡,P = 0.009)。这项初步研究表明,包括听觉神经/脑干诱发电位反应和噪声中的言语感知测试在内的听觉评估应成为与m.3243A>G相关的线粒体疾病患者管理的重要组成部分。那些出现听力障碍以及平衡和头晕相关症状的患者应接受前庭测试和适当管理。