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[格林-巴利综合征中的自主神经受累]

[Autonomic involvement in Guillain-Barré syndrome].

作者信息

Kusunoki Susumu

机构信息

Department of Neurology, Kinki Univerisity School of Medicine.

出版信息

Rinsho Shinkeigaku. 2006 Nov;46(11):878-80.

Abstract

Guillain-Barré syndrome (GBS) is an acute self-limited motor-dominant neuropathy, in which autonomic nervous system is frequently involved. Cardiovascular complications, such as hypertension, hypotension, bradyarrhythmias, and tachyarrythmias, are particularly important because they are sometimes life-threatening. Antiganglioside antibodies are frequently present in the acute-phase sera of GBS. They are considered to be useful for diagnosis and to be involved in the pathogenetic mechanisms. No association between autonomic dysfunction and antiganglioside antibody however has been reported. Recently, we performed the quantitative sudomotor axon reflex test (QSART) in GBS patients and found that patients with high scores in QSART had anti-GQ1b IgG antibodies. It indicates the association between postganglionic sudomotor dysfunction and anti-GQ1b antibodies. Further investigation on larger number of patients is needed to clarify the role of antiganglioside antibodies in the development of autonomic dysfunction.

摘要

吉兰-巴雷综合征(GBS)是一种急性自限性以运动为主的神经病,常累及自主神经系统。心血管并发症,如高血压、低血压、缓慢性心律失常和快速性心律失常,尤为重要,因为它们有时会危及生命。抗神经节苷脂抗体在GBS急性期血清中常存在。它们被认为对诊断有用且参与发病机制。然而,尚未报道自主神经功能障碍与抗神经节苷脂抗体之间存在关联。最近,我们对GBS患者进行了定量汗腺轴突反射试验(QSART),发现QSART得分高的患者有抗GQ1b IgG抗体。这表明节后汗腺运动功能障碍与抗GQ1b抗体之间存在关联。需要对更多患者进行进一步研究,以阐明抗神经节苷脂抗体在自主神经功能障碍发生发展中的作用。

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