Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Lancet Neurol. 2013 Dec;12(12):1180-8. doi: 10.1016/S1474-4422(13)70215-1.
Acute motor axonal neuropathy (AMAN) is a pure motor axonal subtype of Guillain-Barré syndrome (GBS) that was identified in the late 1990s. In Asia and Central and South America, it is the major subtype of GBS, seen in 30-65% of patients. AMAN progresses more rapidly and has an earlier peak than demyelinating GBS; tendon reflexes are relatively preserved or even exaggerated, and autonomic dysfunction is rare. One of the main causes is molecular mimicry of human gangliosides by Campylobacter jejuni lipo-oligosaccharides. In addition to axonal degeneration, electrophysiology shows rapidly reversible nerve conduction blockade or slowing, presumably due to pathological changes at the nodes or paranodes. Autoantibodies that bind to GM1 or GD1a gangliosides at the nodes of Ranvier activate complement and disrupt sodium-channel clusters and axoglial junctions, which leads to nerve conduction failure and muscle weakness. Improved understanding of the disease mechanism and pathophysiology might lead to new treatment options and improve the outlook for patients with AMAN.
急性运动轴索性神经病(AMAN)是吉兰-巴雷综合征(GBS)的纯运动轴索亚型,于 20 世纪 90 年代末被发现。在亚洲和中美洲及南美洲,它是 GBS 的主要亚型,见于 30%-65%的患者。AMAN 的进展比脱髓鞘性 GBS 更快,高峰更早;腱反射相对保留甚至增强,自主神经功能障碍罕见。主要病因之一是空肠弯曲菌脂寡糖与人神经节苷脂的分子模拟。除了轴索变性外,电生理学显示神经传导迅速可逆性阻滞或减慢,可能是由于结或结旁的病理改变。与结旁Ranvier 处 GM1 或 GD1a 神经节苷脂结合的自身抗体激活补体,破坏钠通道簇和轴突-胶质连接,导致神经传导失败和肌无力。对疾病机制和病理生理学的认识的提高可能会带来新的治疗选择,并改善 AMAN 患者的预后。