Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.
CNS Drugs. 2015 Jun;29(6):433-41. doi: 10.1007/s40263-015-0249-8.
Inhibitors of monoamine oxidase-B (MAO-B) occupy an important place in the treatment of Parkinson's disease. Selegiline was the first MAO-B to be used therapeutically, while rasagiline is a second-generation drug with higher potency and selectivity. Safinamide is an investigational MAO-B inhibitor with non-dopaminergic properties that may provide advantages over its predecessors. As a class, MAO-B inhibitors are safe and well tolerated and provide symptomatic benefit both as monotherapy and in combination with other antiparkinsonian medications from early to late stages of disease. In combination with levodopa, MAO-B inhibitors may improve motor fluctuations and allow for lower total doses of levodopa. Patient characteristics and preferences can be important factors in deciding between agents. As a class, MAO-B inhibitors have shown promise as disease-modifying agents, but the clinical trial evidence to date has not been strong enough to afford them such a label. Future research may help further elucidate their relative merits and clarify their role in altering disease progression.
单胺氧化酶-B(MAO-B)抑制剂在帕金森病的治疗中占有重要地位。司来吉兰是第一种被用于治疗的 MAO-B 抑制剂,而雷沙吉兰是一种具有更高效力和选择性的第二代药物。沙芬酰胺是一种具有非多巴胺能特性的研究用 MAO-B 抑制剂,可能比其前身具有优势。作为一类药物,MAO-B 抑制剂安全且耐受良好,无论是单药治疗还是与其他抗帕金森病药物联合使用,从疾病的早期到晚期都能提供症状缓解。与左旋多巴联合使用时,MAO-B 抑制剂可能改善运动波动并允许减少左旋多巴的总剂量。患者的特征和偏好可能是决定药物选择的重要因素。作为一类药物,MAO-B 抑制剂已显示出作为疾病修饰剂的潜力,但迄今为止的临床试验证据还不够强,无法将其归为此类。未来的研究可能有助于进一步阐明它们的相对优势,并阐明它们在改变疾病进展中的作用。