Sheikh Shuja, Alvi Usman, Soliven Betty, Rezania Kourosh
Department of Neurology, University of Chicago, 5841 S. Maryland Avenue, MC 2030, Chicago, IL 60637, USA.
J Clin Med. 2021 Apr 6;10(7):1537. doi: 10.3390/jcm10071537.
Myasthenia gravis (MG) is an autoimmune neuromuscular disorder which is characterized by presence of antibodies against acetylcholine receptors (AChRs) or other proteins of the postsynaptic membrane resulting in damage to postsynaptic membrane, decreased number of AChRs or blocking of the receptors by autoantibodies. A number of drugs such as immune checkpoint inhibitors, penicillamine, tyrosine kinase inhibitors and interferons may induce de novo MG by altering the immune homeostasis mechanisms which prevent emergence of autoimmune diseases such as MG. Other drugs, especially certain antibiotics, antiarrhythmics, anesthetics and neuromuscular blockers, have deleterious effects on neuromuscular transmission, resulting in increased weakness in MG or MG-like symptoms in patients who do not have MG, with the latter usually being under medical circumstances such as kidney failure. This review summarizes the drugs which can cause de novo MG, MG exacerbation or MG-like symptoms in nonmyasthenic patients.
重症肌无力(MG)是一种自身免疫性神经肌肉疾病,其特征是存在针对乙酰胆碱受体(AChRs)或突触后膜其他蛋白质的抗体,导致突触后膜受损、AChRs数量减少或自身抗体阻断受体。许多药物,如免疫检查点抑制剂、青霉胺、酪氨酸激酶抑制剂和干扰素,可能通过改变免疫稳态机制诱导新发MG,这些机制可预防诸如MG等自身免疫性疾病的出现。其他药物,尤其是某些抗生素、抗心律失常药、麻醉剂和神经肌肉阻滞剂,对神经肌肉传递有有害影响,导致MG患者肌无力加重或在无MG的患者中出现MG样症状,后者通常发生在肾衰竭等医疗情况下。本综述总结了可导致新发MG、MG加重或在非重症肌无力患者中出现MG样症状的药物。