Department of Neurology, Haga Hospital, The Hague, The Netherlands.
Expert Rev Clin Immunol. 2010 Nov;6(6):867-74. doi: 10.1586/eci.10.57.
The Lambert-Eaton myasthenic syndrome (LEMS) is an autoimmune disease in which antibodies against voltage-gated calcium channels inhibit cholinergic neurotransmission. LEMS is clinically characterized by muscle weakness and autonomic dysfunction. 3,4-diaminopyridine (3,4-DAP) blocks potassium channels in nerve terminals, resulting in an increase in acetylcholine release. This article describes the four randomized placebo-controlled trials of 3,4-DAP in patients with LEMS. All trials demonstrated a significant effect on muscle strength and compound muscle action potential amplitude. Furthermore, the safety and tolerability of 3,4-DAP are reviewed. The side effects of 3,4-DAP are generally mild and most frequently consist of paresthesias, but epileptic seizures and arrhythmias have been described in patients using high doses. Given the efficacy and safety of 3,4-DAP in LEMS, this drug is the mainstay for symptomatic treatment of LEMS.
Lambert-Eaton 肌无力综合征 (LEMS) 是一种自身免疫性疾病,其中针对电压门控钙通道的抗体抑制胆碱能神经传递。LEMS 的临床特征为肌肉无力和自主功能障碍。3,4-二氨基吡啶 (3,4-DAP) 阻断神经末梢的钾通道,导致乙酰胆碱释放增加。本文描述了 3,4-DAP 在 LEMS 患者中的四项随机安慰剂对照试验。所有试验均显示出对肌肉力量和复合肌肉动作电位幅度的显著影响。此外,还回顾了 3,4-DAP 的安全性和耐受性。3,4-DAP 的副作用通常较轻,最常见的是感觉异常,但在使用高剂量的患者中已描述了癫痫发作和心律失常。鉴于 3,4-DAP 在 LEMS 中的疗效和安全性,该药是 LEMS 症状治疗的主要药物。