Department of Neurodegeneration, Hertie Institute for Clinical Brain Research, University of Tübingen, Germany & Center for Neurology, University Hospital Tübingen, Germany; Centre for Neuroscience of Speech, The University of Melbourne, Victoria, Australia; Redenlab, Melbourne, Australia.
Department of Neurodegeneration, Hertie Institute for Clinical Brain Research, University of Tübingen, Germany & Center for Neurology, University Hospital Tübingen, Germany; Therapiezentrum, University Hospital Tübingen, Germany.
Mitochondrion. 2017 Nov;37:1-7. doi: 10.1016/j.mito.2017.06.002. Epub 2017 Jun 19.
Mutations in the nuclear-encoded mitochondrial DNA polymerase gamma (POLG) can result in a wide spectrum of neurological deficits. A common presentation is progressive ataxia (POLG-A) which includes impaired speech and swallowing. The nature, severity and impact of these deficits in POLG-A is not known. A comprehensive quantitative and qualitative characterization of dysarthria and dysphagia in this recurrent ataxia disorder will assist in diagnostics, provide insights into the underlying pathology, and establish the foundation for future therapy trials.
14 consecutive patients with POLG (9 females, mean age=50.1y, SD=11.2) and 34 healthy controls were enrolled. Comprehensive assessments of motor speech and swallowing function, acoustic analysis of speech, videofluoroscopy and measures of quality of life were conducted.
The speech profile of individuals with POLG-A was characterized by poor control of pitch and strain-strangled voice quality, reduced rate of speech and longer variable silences between words, and articulatory breakdown including imprecise consonants and vowel distortions. Swallowing deficits included slower initiation of the swallow reflex, poor control of bolus and late epiglottic closure. Speech and swallowing related quality of life was worse than healthy controls.
The dysarthria and dysphagia profiles in POLG-A are largely symptomatic of impaired timing, indicating a mainly spinocerebellar deficit. Dysarthria and dysphagia contribute to a significant impairment in functional quality of life, and progress distinctly from other POLG-A dysfunctions like ataxia or cognitive impairment. Our assessments establish meaningful patient focused outcome measures that will be suitable for use in natural history studies and clinical trials.
核编码线粒体 DNA 聚合酶 γ(POLG)的突变可导致广泛的神经功能缺损。常见的表现为进行性共济失调(POLG-A),包括言语和吞咽障碍。POLG-A 中这些缺陷的性质、严重程度和影响尚不清楚。对这种复发性共济失调疾病的构音障碍和吞咽困难进行全面的定量和定性描述,将有助于诊断,深入了解潜在的病理,并为未来的治疗试验奠定基础。
连续纳入 14 名 POLG 患者(9 名女性,平均年龄 50.1 岁,标准差 11.2)和 34 名健康对照者。对运动言语和吞咽功能、言语声学分析、视频透视和生活质量进行全面评估。
POLG-A 患者的言语特征为音高和张力性声音质量控制差、言语率降低、单词之间的可变停顿时间延长,以及包括不精确辅音和元音扭曲在内的发音障碍。吞咽缺陷包括吞咽反射启动缓慢、食团控制不佳和会厌后期关闭不良。言语和吞咽相关的生活质量比健康对照组差。
POLG-A 中的构音障碍和吞咽困难主要是由于时间控制受损引起的,表明主要是脊髓小脑缺陷。构音障碍和吞咽困难导致功能生活质量显著受损,并明显不同于其他 POLG-A 功能障碍,如共济失调或认知障碍。我们的评估建立了有意义的以患者为中心的结果测量方法,这些方法将适用于自然史研究和临床试验。