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肌肉特异性激酶抗体阳性重症肌无力的重复神经刺激

Repetitive Nerve Stimulation in MuSK-Antibody-Positive Myasthenia Gravis.

作者信息

Kim Seung Woo, Sunwoo Mun Kyung, Kim Seung Min, Shin Ha Young, Sunwoo Il Nam

机构信息

Department of Neurology, Yonsei University College of Medicine, Seoul, Korea.

Department of Neurology, Bundang Jesaeng General Hospital, Seongnam, Korea.

出版信息

J Clin Neurol. 2017 Jul;13(3):287-292. doi: 10.3988/jcn.2017.13.3.287. Epub 2017 May 15.

Abstract

BACKGROUND AND PURPOSE

Responses to repetitive nerve stimulation (RNS) in patients with muscle-specific tyrosine kinase (MuSK) antibody (Ab)-positive myasthenia gravis (MG) vary depending on the muscles tested. We analyzed the RNS responses of limb and facial muscles in MuSK-Ab-positive and acetylcholine receptor (AChR)-Ab-negative MG (MuSK MG) and MuSK-Ab-negative and AChR-Ab-negative [double-seronegative (DSN)] MG patients.

METHODS

We retrospectively compared RNS responses between 45 MuSK MG and 29 DSN MG. RNS was applied to the abductor digiti minimi, flexor carpi ulnaris, trapezius, orbicularis oculi, and nasalis muscles.

RESULTS

Abnormal RNS responses in limb muscles were observed in 22.2 and 58.6% of MuSK MG and DSN MG patients, respectively, with abnormal facial responses observed in 77.8 and 65.5%, and abnormal responses observed in any of the five muscles in 86.7 and 72.4%. Abnormal RNS responses in the abductor digiti minimi or flexor carpi ulnaris were less frequent in MuSK MG (8.9 and 15.6%, respectively) than in DSN MG (37.9 and 55.2%), whereas the findings for other muscles were not significantly different between the groups. Abnormal facial responses but normal limb responses were independently associated with MuSK MG (odds ratio=5.224, 95% confidence interval=1.300-20.990).

CONCLUSIONS

Abnormal RNS responses primarily in facial muscles without involvement of limb muscles were more pronounced in MuSK MG than in DSN MG. RNS of both facial and limb muscles in AChR-Ab-negative MG can increase the test sensitivity and aid in early suspicion of MuSK MG.

摘要

背景与目的

肌肉特异性酪氨酸激酶(MuSK)抗体(Ab)阳性的重症肌无力(MG)患者对重复神经刺激(RNS)的反应因所检测的肌肉不同而有所差异。我们分析了MuSK抗体阳性且乙酰胆碱受体(AChR)抗体阴性的MG(MuSK MG)患者以及MuSK抗体阴性且AChR抗体阴性的[双血清阴性(DSN)]MG患者四肢和面部肌肉的RNS反应。

方法

我们回顾性比较了45例MuSK MG患者和29例DSN MG患者的RNS反应。RNS应用于小指展肌、尺侧腕屈肌、斜方肌、眼轮匝肌和鼻肌。

结果

MuSK MG患者和DSN MG患者四肢肌肉RNS异常反应分别为22.2%和58.6%,面部异常反应分别为77.8%和65.5%,五种肌肉中任何一种出现异常反应分别为86.7%和72.4%。MuSK MG患者小指展肌或尺侧腕屈肌的RNS异常反应(分别为8.9%和15.6%)比DSN MG患者(分别为37.9%和55.2%)少见,而两组其他肌肉的结果无显著差异。面部反应异常但四肢反应正常与MuSK MG独立相关(比值比=5.224,95%置信区间=1.300 - 20.990)。

结论

主要为面部肌肉RNS异常反应而无四肢肌肉受累在MuSK MG中比在DSN MG中更明显。AChR抗体阴性MG患者面部和四肢肌肉的RNS检查可提高检测敏感性,有助于早期怀疑MuSK MG。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfc3/5532326/93f900a42a0a/jcn-13-287-g001.jpg

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