Leon-Sarmiento Fidias E, Leon-Ariza Daniel S, Doty Richard L
Smell and Taste Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
J Clin Neuromuscul Dis. 2013 Sep;15(1):1-6. doi: 10.1097/CND.0b013e31829e22ba.
Myasthenia gravis has traditionally been viewed as a disorder that solely affects the neuromuscular junction within the peripheral nervous system. However, there is now evidence that the cholinergic dysfunction of this disorder may be more widespread than previously believed. This article provides a systematic review of the studies that examined smell and taste function in myasthenia gravis.
We analyzed studies that reported chemosensory function alterations in patients with myasthenia gravis. PubMed, MEDLINE, Web of Science, EMBASE, and SciELO, searched to identify articles published from January 1950 through December 2012, were supplemented by relevant articles. The following information was identified from each article: the number of patients, number of controls (if any), clinical stage of patients, neurological involvement, serological state, taste or smell involvement, chemosensory test used, and country of publication.
Ten studies reporting smell and taste function and dysfunction in patients with myasthenia gravis were identified, most of which were case reports commenting on apparent abnormalities in the taste system. The sole empirical study that investigated taste function, however, was negative, suggesting that some reports of taste loss may reflect olfactory loss. One study clearly documented olfactory dysfunction in patients with myasthenia gravis, dysfunction most likely attributable to altered central nervous system cholinergic function.
Chemosensory dysfunction has been reported in a number of patients with myasthenia gravis. Given the close association between complaints of taste dysfunction and loss of flavor sensations secondary to olfactory system damage, quantitative testing should be used to accurately assess the nature and degree of the dysfunction present in this debilitating disorder.
传统上,重症肌无力被视为一种仅影响外周神经系统神经肌肉接头的疾病。然而,现在有证据表明,这种疾病的胆碱能功能障碍可能比之前认为的更为广泛。本文对研究重症肌无力嗅觉和味觉功能的相关研究进行了系统综述。
我们分析了报告重症肌无力患者化学感觉功能改变的研究。通过检索PubMed、MEDLINE、科学网、EMBASE和SciELO来识别1950年1月至2012年12月发表的文章,并辅以相关文章。从每篇文章中提取以下信息:患者数量、对照数量(若有)、患者临床分期、神经受累情况、血清学状态、味觉或嗅觉受累情况、所使用的化学感觉测试以及发表国家。
共识别出10项报告重症肌无力患者嗅觉和味觉功能及功能障碍的研究,其中大多数是病例报告,评论了味觉系统中明显的异常情况。然而,唯一一项研究味觉功能的实证研究结果为阴性,这表明一些味觉丧失的报告可能反映的是嗅觉丧失。一项研究明确记录了重症肌无力患者存在嗅觉功能障碍,这种功能障碍很可能归因于中枢神经系统胆碱能功能改变。
已有多项研究报告了重症肌无力患者存在化学感觉功能障碍。鉴于味觉功能障碍主诉与嗅觉系统损伤继发的味觉丧失之间密切相关,应采用定量测试来准确评估这种致残性疾病中功能障碍的性质和程度。