Hintze Justin M, Ludlow Christy L, Bansberg Stephen F, Adler Charles H, Lott David G
1 Head and Neck Regeneration Program, Center for Regenerative Medicine, Mayo Clinic Arizona, Phoenix, Arizona, USA.
2 Department of Communication Sciences and Disorders, James Madison University, Virginia, USA.
Otolaryngol Head Neck Surg. 2017 Oct;157(4):551-557. doi: 10.1177/0194599817728521. Epub 2017 Aug 29.
Objective The purpose of this review is to describe the recent advances in identifying possible factors involved in the pathogenesis of spasmodic dysphonia. Spasmodic dysphonia is a task-specific focal laryngeal dystonia characterized by irregular and uncontrolled voice breaks. Pathogenesis of the disorder is poorly understood. Data Sources PubMed, Google Scholar, and Cochrane Library. Review Methods The data sources were searched using the following search terms: ( spasmodic dysphonia or laryngeal dystonia) and ( etiology, aetiology, diagnosis, pathogenesis, or pathophysiology). Conclusions Several potential etiological factors have been proposed by epidemiological, genetic, and neuropathological studies. Spasmodic dysphonia is a rare disorder primarily affecting females beginning in their 40s. Vocal tremor co-occurs in 30% to 60%. Large cohort studies identified risk factors such as a family history of neurological disorders including dystonia and tremor, recent viral illness, and heavy voice use. As none are rare events, a complex interactive process may contribute to pathogenesis in a small proportion of those at risk. Consequences to pathogenesis are neurological processes found in spasmodic dysphonia: loss of cortical inhibition, sensory processing disturbances, and neuroanatomical and physiological differences in the laryngeal motor control system. Implications for Practice Diagnosis of spasmodic dysphonia usually includes speech and laryngoscopic assessment. However, as diagnosis is sometimes problematic, measurement of neurophysiological abnormalities may contribute useful adjuncts for the diagnosis of spasmodic dysphonia in the future.
目的 本综述旨在描述在确定痉挛性发声障碍发病机制中可能涉及的因素方面的最新进展。痉挛性发声障碍是一种特定任务的局灶性喉肌张力障碍,其特征为声音不规则且不受控制地中断。该疾病的发病机制尚不清楚。
数据来源 PubMed、谷歌学术和考克兰图书馆。
综述方法 使用以下检索词对数据来源进行检索:(痉挛性发声障碍或喉肌张力障碍)以及(病因、病原学、诊断、发病机制或病理生理学)。
结论 流行病学、遗传学和神经病理学研究提出了几种潜在的病因因素。痉挛性发声障碍是一种罕见疾病,主要影响40多岁的女性。30%至60%的患者会同时出现声带震颤。大型队列研究确定了一些风险因素,如包括肌张力障碍和震颤在内的神经系统疾病家族史、近期病毒感染以及过度用嗓。由于这些都并非罕见事件,一个复杂的相互作用过程可能在一小部分有风险的人群中导致发病机制。痉挛性发声障碍中发现的神经学过程对发病机制的影响包括:皮质抑制丧失、感觉处理障碍以及喉运动控制系统的神经解剖学和生理学差异。
对实践的启示 痉挛性发声障碍的诊断通常包括言语和喉镜评估。然而,由于诊断有时存在问题,神经生理异常的测量未来可能有助于痉挛性发声障碍的诊断。