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The Shaking Palsy of the Larynx—Potential Biomarker for Multiple System Atrophy: A Pilot Study and Literature Review

机译:颤抖的麻痹—多系统萎缩的潜在生物标志物:一项初步研究和文献综述

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摘要

In its early stages multiple system atrophy (MSA), a neurodegenerative movement disorder, can be difficult to differentiate from idiopathic Parkinson's disease (PD), and emphasis has been put on identifying premotor symptoms to allow for its early identification. The occurrence of vegetative symptoms in addition to motor impairment, such as orthostatic hypotension and neurogenic bladder dysfunction, enable the clinical diagnosis in the advanced stages of the disease. Usually with further disease progression, laryngeal abnormalities become clinically evident and can manifest in laryngeal stridor due to impaired vocal fold motion, such as vocal fold abduction restriction, mostly referred to as vocal fold paresis, or paradoxical vocal fold adduction during inspiration. While the pathogenesis of laryngeal stridor is discussed controversially, its occurrence is clearly associated with reduced life expectancy. Before the clinical manifestation of laryngeal dysfunction however, abnormal vocal fold motion can already be seen in patients that might not yet fulfill the diagnostic criteria of MSA. In this article we summarize the current literature on pharyngolaryngeal findings in MSA and report preliminary findings from a pilot study investigating eight consecutive MSA patients. Patients showed varying speech abnormalities. Only 2/8 patients exhibited laryngeal stridor. However, during FEES, all patients presented with irregular arytenoid cartilages movements and vocal fold abduction restriction. 3/8 showed vocal fold fixation and 1/8 paradoxical vocal fold motion. All patients presented with oropharyngeal dysphagia, 5/8 with penetration or aspiration events. We suggest that specific abnormal vocal fold motion can help identifying MSA patients and may allow for delimiting this disorder from idiopathic PD. These findings therefore may serve as a novel clinical biomarker for MSA. Based on the available data and our preliminary clinical experience we developed a standardized easy-to-implement task-protocol to be performed during flexible endoscopic evaluation of swallowing (FEES) for detection of MSA-related pharyngolaryngeal movement disorders. Furthermore, we initiated a prospective study to evaluate the diagnostic utility of this protocol.
机译:在其早期阶段,神经退行性运动障碍多系统萎缩症(MSA)可能很难与特发性帕金森氏病(PD)区分开,并且重点已经放在了识别运动前症状上,以便对其进行早期识别。除运动功能障碍外,植物性症状的发生,如体位性低血压和神经源性膀胱功能障碍,也使该病晚期的临床诊断成为可能。通常随着疾病的进一步发展,喉部异常在临床上变得很明显,并且由于声带运动受损(例如,声带外展受限,通常被称为声带麻痹或吸气过程中的悖论性声带内收)而在喉str中表现出来。虽然对喉str喘鸣的发病机理进行了有争议的讨论,但它的出现显然与预期寿命缩短有关。但是,在临床表现为喉功能不全之前,可能尚未达到MSA诊断标准的患者已经发现异常的声带运动。在本文中,我们总结了有关MSA中咽喉部发现的最新文献,并报告了一项调查性研究的初步发现,该研究调查了8名连续MSA患者。患者表现出各种语音异常。只有2/8例患者表现出喉str气。但是,在FEES期间,所有患者均出现不规则的类软骨软骨运动和声带外展受限。 3/8显示声带固定和1/8矛盾的声带运动。所有患者均出现口咽吞咽困难,5/8发生渗透或误吸事件。我们建议特定的异常声带运动可以帮助识别MSA患者,并且可以将这种疾病与特发性PD区别开来。因此,这些发现可以作为MSA的新型临床生物标志物。基于现有数据和我们的初步临床经验,我们制定了一项标准化的易于实施的任务协议,该协议将在吞咽内窥镜评估吞咽(FEES)的过程中执行,以检测MSA相关的咽喉运动障碍。此外,我们启动了一项前瞻性研究,以评估该协议的诊断效用。

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