Molgó J, Guglielmi J M
Laboratoire de Neurobiologie Cellulaire et Moléculaire, C.N.R.S., Gif-sur-Yvette, France.
Pflugers Arch. 1996;431(6 Suppl 2):R295-6. doi: 10.1007/BF02346385.
The Lambert-Eaton myasthenic syndrome (LEMS) is a rare autoimmune disease of peripheral cholinergic transmission that results in muscle weakness and autonomic dysfunction, due to impaired acetylcholine release. A review of available clinical information indicates that 3,4-diaminopyridine (3,4-DAP) used either alone or in conjunction with other therapies was effective in treating the motor and the autonomic deficits in patients with primary and paraneoplastic LEMS of varying degrees of severity. A survey of the medical literature indicates that about 150 patients have been treated worldwide with 3,4-DAP. The general view is that 3,4-DAP is well tolerated in short- or long-term treatments, with only mild side effects. 3,4-DAP is an orphan drug approved for clinical use in many european countries that lacks adoptive parents because its exploitation is not profitable.
兰伯特-伊顿肌无力综合征(LEMS)是一种罕见的外周胆碱能传递自身免疫性疾病,由于乙酰胆碱释放受损,导致肌肉无力和自主神经功能障碍。对现有临床信息的回顾表明,单独使用或与其他疗法联合使用的3,4-二氨基吡啶(3,4-DAP)可有效治疗不同严重程度的原发性和副肿瘤性LEMS患者的运动和自主神经功能缺陷。对医学文献的一项调查表明,全球约有150名患者接受了3,4-DAP治疗。普遍观点认为,3,4-DAP在短期或长期治疗中耐受性良好,只有轻微副作用。3,4-DAP是一种在许多欧洲国家被批准用于临床的孤儿药,由于其开发无利可图而缺乏采用者。