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抗水通道蛋白4抗体阳性和阴性多发性硬化症患者的多模态诱发电位研究

Multimodality-evoked potential study of anti-aquaporin-4 antibody-positive and -negative multiple sclerosis patients.

作者信息

Watanabe Akihiro, Matsushita Takuya, Doi Hikaru, Matsuoka Takashi, Shigeto Hiroshi, Isobe Noriko, Kawano Yuji, Tobimatsu Shozo, Kira Jun-ichi

机构信息

Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, Japan.

出版信息

J Neurol Sci. 2009 Jun 15;281(1-2):34-40. doi: 10.1016/j.jns.2009.02.371. Epub 2009 Apr 1.

Abstract

Neuromyelitis optica (NMO) is claimed to be a distinct disease entity from multiple sclerosis (MS) because of its strong association with NMO-IgG/anti-AQP4 antibody; however, the in vivo role of the antibody remains unknown. Therefore, we aimed to clarify whether the presence of anti-AQP4 antibody is associated with any abnormalities in multimodality-evoked potentials in 111 patients with relapsing-remitting or relapsing-progressive MS, including the opticospinal form of MS, 18 of whom were seropositive for anti-AQP4 antibody. More patients with anti-AQP4 antibody showed a lack of the P100 component on visual-evoked potentials (VEPs) than those without the antibody (11/17, 64.7% vs. 20/84, 23.8%, p=0.003), whereas the frequency of delayed P100 latency was significantly higher in the latter group than in the former (1/17, 5.9% vs. 28/84, 33.3%, p=0.021). The frequencies of non-responses and delayed central sensory conduction times in median and posterior tibial nerve somatosensory-evoked potentials (SEPs) were not significantly different between anti-AQP4 antibody-positive and -negative patients. In terms of upper and lower limb motor-evoked potentials (MEPs), the frequencies of non-responses and delayed central motor conduction times did not differ significantly based on the presence or absence of anti-AQP4 antibody. The frequency of optic nerve lesions on MRI was significantly higher in anti-AQP4 antibody-positive patients than in anti-AQP4 antibody-negative patients (p=0.0137). Multiple logistic analyses revealed that anti-AQP4 antibody positivity (OR=8.406, p=0.02) and unevoked VEP responses (OR=35.432, p<0.001) were significantly related to development of severe visual impairment. Such an association of anti-AQP4 antibody with disability was not found for either severe motor or sensory impairment. These findings suggest a distinctive nature of optic nerve lesions between anti-AQP4 antibody-positive and -negative patients; lesions are supposed to be more necrotic in the former group and more demyelinating in the latter.

摘要

视神经脊髓炎(NMO)因其与NMO-IgG/抗水通道蛋白4(AQP4)抗体密切相关,被认为是一种与多发性硬化症(MS)不同的疾病实体;然而,该抗体在体内的作用仍不清楚。因此,我们旨在明确111例复发缓解型或复发进展型MS患者(包括视神经脊髓型MS)中,抗AQP4抗体的存在是否与多模态诱发电位的任何异常有关,其中18例抗AQP4抗体血清学阳性。与无该抗体的患者相比,更多抗AQP4抗体阳性患者在视觉诱发电位(VEP)上缺乏P100成分(11/17,64.7% 对 20/84,23.8%,p = 0.003),而后者组中P100潜伏期延迟的频率显著高于前者(1/17,5.9% 对 28/84,33.3%,p = 0.021)。抗AQP4抗体阳性和阴性患者在正中神经和胫后神经体感诱发电位(SEP)中的无反应频率及中枢感觉传导时间延迟频率无显著差异。在上肢和下肢运动诱发电位(MEP)方面,基于抗AQP4抗体的有无,无反应频率及中枢运动传导时间延迟频率无显著差异。抗AQP4抗体阳性患者MRI上视神经病变的频率显著高于抗AQP4抗体阴性患者(p = 0.0137)。多项逻辑分析显示,抗AQP4抗体阳性(比值比[OR]=8.406,p = 0.02)和VEP无诱发反应(OR = 35.432,p<0.001)与严重视力损害的发生显著相关。对于严重运动或感觉损害,未发现抗AQP4抗体与残疾有此类关联。这些发现提示抗AQP4抗体阳性和阴性患者视神经病变具有独特性质;在前一组中病变可能更具坏死性,而在后一组中更具脱髓鞘性。

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