Department of Molecular Neurology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Department of Neurology, University Hospital of Würzburg, Würzburg, Germany.
J Neural Transm (Vienna). 2023 Jun;130(6):847-861. doi: 10.1007/s00702-023-02623-8. Epub 2023 Mar 24.
Inhibitors of monoamine oxidase B (MAO-B) and catechol-O-methyltransferase (COMT) are major strategies to reduce levodopa degradation and thus to increase and prolong its effect in striatal dopaminergic neurotransmission in Parkinson's disease patients. While selegiline/rasagiline and tolcapone/entacapone have been available on the market for more than one decade, safinamide and opicapone have been approved in 2015 and 2016, respectively. Meanwhile, comprehensive data from several post-authorization studies have described the use and specific characteristics of the individual substances in clinical practice under real-life conditions. Here, we summarize current knowledge on both medication classes, with a focus on the added clinical value in Parkinson's disease. Furthermore, we outline practical considerations in the treatment of motor fluctuations and provide an outlook on ongoing studies with MAO-B and COMT inhibitors.
单胺氧化酶 B(MAO-B)和儿茶酚-O-甲基转移酶(COMT)抑制剂是减少左旋多巴降解的主要策略,从而增加和延长其在帕金森病患者纹状体多巴胺能神经传递中的作用。虽然司来吉兰/雷沙吉兰和托卡朋/恩他卡朋已经上市十多年,但沙非酰胺和奥匹卡朋分别于 2015 年和 2016 年获得批准。与此同时,几项上市后研究的综合数据描述了在现实条件下临床实践中使用的个体药物的具体特点。在这里,我们总结了这两类药物的现有知识,重点介绍了在帕金森病中的附加临床价值。此外,我们还概述了在治疗运动波动方面的实际考虑因素,并对正在进行的 MAO-B 和 COMT 抑制剂研究进行了展望。