Rudnicki S, Vriesendorp F, Koski C L, Mayer R F
Department of Neurology, University of Maryland School of Medicine, Baltimore.
Muscle Nerve. 1992 Jan;15(1):57-62. doi: 10.1002/mus.880150111.
Nerve conduction studies (NCS) and antiperipheral nerve myelin antibody (A-PNM Ab) titers were measured serially in 29 patients with Guillain-Barré syndrome (GBS), of whom 21 were treated with plasmapheresis. Data were obtained from 3 to 6 days until 1 to 2 years after onset of symptoms. Within 3 to 6 days, mean NCS were abnormal. They improved some by 1 week and became maximally abnormal by 4 to 8 weeks, during which time A-PNM Ab fell to low levels. In 5 patients plasmapheresed, A-PNM Ab fell and then increased at 4 to 8 weeks, followed by significant deterioration of NCS (P = 0.01) compared with those without antibody rebound at 18 weeks. These results suggest that, in monophasic GBS, there may be two mechanisms of conduction dysfunction such as early paranodal retraction and later demyelination. In some patients plasmapheresed, A-PNM Ab may rebound associated with further conduction dysfunction. These patients may benefit from further plasmapheresis.
对29例吉兰-巴雷综合征(GBS)患者进行了连续的神经传导研究(NCS)和抗周围神经髓鞘抗体(A-PNM Ab)滴度检测,其中21例接受了血浆置换治疗。数据收集时间为症状出现后3至6天直至1至2年。在3至6天内,平均NCS异常。到1周时有所改善,4至8周时异常程度达到最大,在此期间A-PNM Ab降至低水平。在5例接受血浆置换的患者中,A-PNM Ab在4至8周时下降然后升高,与18周时无抗体反弹的患者相比,随后NCS显著恶化(P = 0.01)。这些结果表明,在单相GBS中,可能存在两种传导功能障碍机制,如早期节旁退缩和后期脱髓鞘。在一些接受血浆置换的患者中,A-PNM Ab可能反弹并伴有进一步的传导功能障碍。这些患者可能从进一步的血浆置换中获益。