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首页> 外文期刊>Clinical neurophysiology >A-waves in Guillain-Barré syndrome: Correlation with electrophysiological subtypes and antiganglioside antibodies
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A-waves in Guillain-Barré syndrome: Correlation with electrophysiological subtypes and antiganglioside antibodies

机译:Guillain-Barré综合征的A波:与电生理亚型和抗神经节苷脂抗体的相关性

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Objective: To investigate the relationship of A-waves with conventional electrophysiological subtypes of Guillain-Barré syndrome (GBS), as well as with anti-ganglioside antibodies. Methods: The subjects consisted of 30. GBS patients who were classified into acute inflammatory demyelinating polyradiculoneuropathy (AIDP), acute motor axonal neuropathy, and unclassified based on the results of nerve conduction studies. " Abundant A-waves" were defined for the upper-limb nerves (median and ulnar nerves) using receiver-operator characteristic curves. The presence or absence of IgG anti-ganglioside antibodies was also noted. Results: Abundant A-waves at weeks 3-6 from onset were observed in 64% of the 14 AIDP patients and 0% of 16 non-AIDP patients, and in 60% of 15 antibody-negative patients and 0% of 15 antibody-positive patients. In the earlier period, this relationship was less clear. The correlation between the conventional electrophysiological subtypes and antibodies was present, but was much weaker. Conclusions: Abundant A-waves in GBS after the acute phase were strongly associated with demyelination that was not mediated by antiganglioside antibodies, possibly through the mechanism of proximal re-excitation induced by electrical inhomogeneities due to segmental demyelination. Significance: Abundant A-waves are promising as a novel reliable marker of demyelination.
机译:目的:探讨A波与格林-巴利综合征(GBS)的常规电生理亚型以及抗神经节苷脂抗体的关系。方法:研究对象包括30例GBS患者,根据神经传导研究的结果将其分为急性炎症性脱髓鞘性多发性神经根神经病(AIDP),急性运动性轴索神经病和未分类。使用接收者-操作者特征曲线为上肢神经(中神经和尺神经)定义了“丰富的A波”。还注意到了IgG抗神经节苷脂抗体的存在或不存在。结果:从发病开始的第3-6周,在14例AIDP患者中有64%以及16例非AIDP患者中有0%以及15例抗体阴性患者中的60%和15例抗体中0%观察到大量的A波阳性患者。在早期,这种关系还不太清楚。存在常规电生理亚型和抗体之间的相关性,但弱得多。结论:急性期后GBS中大量的A波与脱髓鞘作用密切相关,这不是由抗神经节苷脂抗体介导的,可能是由于节段性脱髓鞘引起的电不均匀性引起的近端再激发机制。启示:丰富的A波有望作为一种新型的脱髓鞘可靠标记。

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