重症肌无力患者的记忆和认知障碍

L. Susanti
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摘要

重症肌无力(MG)是一种发生在神经肌肉交界处的自身免疫性疾病。这是一种相对罕见的疾病,其特征是波动性肌肉无力,在用力时最严重,休息后好转。这种疾病是可以治疗的,但可导致显著的发病率和死亡率。MG的病因通常是获得性自身免疫,但在某些情况下,由神经肌肉连接处的遗传异常引起MG的发病率约为4.1-30万/年,患病率为150-200 /百万人据信,在过去的70年里,MG的发病率在全球范围内有所增加。1915年至1934年,MG的发病率估计为20万分之一,1934年抗胆碱酯酶药物问世后,MG的发病率上升到2万分之一,1969年发现AChR抗体后,MG的发病率上升到1.7万分之一。性别和年龄似乎影响重症肌无力的发生。40岁以下,男女比例约为3:1;然而,在40到50岁之间,以及在青春期,这是大致相等的。50岁以上,多见于男性重症肌无力患者的认知障碍仍然是一个有争议的问题。有证据表明重症肌无力涉及中枢神经系统,导致认知障碍——近60%的重症肌无力患者报告有记忆困难Klaus et al., 2022对重症肌无力的研究表明,患者的大脑结构和功能发生了变化。结构变化表现为扣带回、下顶叶和梭状回灰质体积显著减少。功能改变的特征是认知功能、工作记忆和体感相关的空间定向能力下降
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Memory and Cognitive Impairment in Myasthenia Gravis
Myasthenia gravis (MG) is an autoimmune disease in the neuromuscular junction. This is a relatively uncommon disorder characterized by fluctuating muscle weakness, worst with exertion and improves with rest. This disease is treatable but can result in significant morbidity and mortality. The etiology of  MG is commonly acquired autoimmune but, in some case, result from genetic abnormalities in the neuromuscular junction.1 The incidence of  MG  is about 4.1-30 points million per year, and the prevalence rate ranges from 150-200 cases per million.2  It is believed that MG incidence has increased worldwide over the past seven decades. The majority of MG was estimated at 1 in 200,000 from 1915 to 1934, grew to 1 per 20,000 after the introduction of anticholinesterase drugs in 1934, and rose to 1 per 17,000 population after the discovery of AChR antibodies in 1969.3 Sex and age appear to influence the occurrence of myasthenia gravis. Below 40 years of age, the female: male ratio is about 3: 1; however, between 40 and 50 years, as well as during puberty, it is roughly equal. Over 50 years, it occurs more commonly in males.3             Cognitive impairment in patients with myasthenia gravis is still a matter of debate. There is some evidence that central nervous system involvement in myasthenia gravis contributes to cognitive impairment—nearly 60% of individuals with MG report memory difficulties.4 Mao et al. reported in their metanalysis study that patients with suspected MG performed worse than healthy controls regarding verbal learning and memory.5 Research by Klaus et al., 2022 on myasthenia gravis showed structural and functional changes in the patient's brain. Structural changes were seen in the form of a significant decrease in the volume of gray matter in the cingulate gyrus, inferior parietal lobe, and fusiform gyrus. Functional changes are characterized by decreased performance in cognitive function, working memory, and somatosensory-related spatial orientation.6
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