Warnecke Tobias, Vogel Annemarie, Ahring Sigrid, Gruber Doreen, Heinze Hans-Jochen, Dziewas Rainer, Ebersbach Georg, Gandor Florin
Department of Neurology, University of Münster, Münster, Germany.
Hospital for Movement Disorders/Parkinson's Disease, Beelitz-Heilstätten, Germany.
Front Neurol. 2019 Mar 26;10:241. doi: 10.3389/fneur.2019.00241. eCollection 2019.
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.
多系统萎缩(MSA)是一种神经退行性运动障碍,在其早期阶段,很难与特发性帕金森病(PD)区分开来,因此人们一直强调识别运动前症状以实现早期诊断。除运动障碍外,还出现植物神经症状,如体位性低血压和神经源性膀胱功能障碍,这有助于在疾病晚期进行临床诊断。通常随着疾病的进一步发展,喉部异常在临床上变得明显,可表现为由于声带运动受损导致的喉喘鸣,如声带外展受限,大多称为声带轻瘫,或吸气时反常性声带内收。虽然喉喘鸣的发病机制存在争议,但其发生显然与预期寿命缩短有关。然而,在喉部功能障碍临床表现之前,在可能尚未符合MSA诊断标准的患者中已经可以看到异常的声带运动。在本文中,我们总结了目前关于MSA咽喉部表现的文献,并报告了一项对8例连续MSA患者进行的初步研究的初步结果。患者表现出不同的言语异常。只有2/8的患者出现喉喘鸣。然而,在纤维内镜吞咽功能检查(FEES)期间,所有患者均表现出杓状软骨运动不规则和声带外展受限。3/8表现为声带固定,1/8表现为反常性声带运动。所有患者均出现口咽吞咽困难,5/8出现误吸或呛咳事件。我们认为,特定的异常声带运动有助于识别MSA患者,并可能有助于将这种疾病与特发性PD区分开来。因此,这些发现可能成为MSA的一种新的临床生物标志物。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,用于在吞咽功能的柔性内镜评估(FEES)期间检测与MSA相关的咽喉部运动障碍。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。