Sanders D B, Cao L, Massey J M, Juel V C, Hobson-Webb L, Guptill J T
Neuromuscular Division, Department of Neurology, Duke University Medical Center, Durham, NC, USA.
Neuromuscular Division, Department of Neurology, Duke University Medical Center, Durham, NC, USA.
Clin Neurophysiol. 2014 Jun;125(6):1274-7. doi: 10.1016/j.clinph.2013.11.007. Epub 2013 Nov 16.
We reviewed our experience to determine if the decremental pattern during low frequency repetitive nerve stimulation (LF-RNS) distinguishes between the Lambert-Eaton myasthenic syndrome (LEMS) and myasthenia gravis (MG).
LF-RNS studies were reviewed from 34 LEMS and 44 MG patients, 4 of whom had antibodies to muscle specific kinase (MuSK). In each train we calculated the ratio between the early and the later decrement. Receiver-operator characteristic curves were calculated to determine the ratio that best distinguished between LEMS and MG.
The late decrement was more often greater in LEMS and the converse was true in MG, but with some overlap in values in individual patients. A late decrement more than 102% of the early decrement discriminated between LEMS and MG in 90% of studies. The decremental pattern in MG patients with MuSK antibodies resembled that in LEMS.
When the decrement becomes progressively greater during low frequency RNS, the patient is more likely to have LEMS than MG, and in MG, is more likely to have MuSK antibodies.
A progressive decrement in patients otherwise felt to have MG should prompt further clinical, serological and electrodiagnostic tests. Further studies are needed to assess the decremental pattern in MuSK MG.
我们回顾了自身经验,以确定低频重复神经刺激(LF-RNS)期间的递减模式是否能区分兰伯特-伊顿肌无力综合征(LEMS)和重症肌无力(MG)。
回顾了34例LEMS患者和44例MG患者的LF-RNS研究,其中4例MG患者有肌肉特异性激酶(MuSK)抗体。在每次刺激序列中,我们计算早期递减与晚期递减的比值。计算受试者操作特征曲线,以确定最能区分LEMS和MG的比值。
LEMS患者中晚期递减更常见,MG患者则相反,但个别患者的值有一定重叠。在90%的研究中,晚期递减超过早期递减的102%可区分LEMS和MG。有MuSK抗体的MG患者的递减模式与LEMS患者相似。
当低频RNS期间递减逐渐增大时,患者更可能患LEMS而非MG,而在MG患者中,更可能有MuSK抗体。
在其他方面被认为患有MG的患者中,递减逐渐增大应促使进行进一步的临床、血清学和电诊断检查。需要进一步研究来评估MuSK MG中的递减模式。