{"title":"Istradefylline: A novel agent in the treatment of \"off\" episodes associated with levodopa/carbidopa use in Parkinson disease.","authors":"Lauren Cummins, Marshall E Cates","doi":"10.9740/mhc.2022.01.032","DOIUrl":null,"url":null,"abstract":"<p><p>The current gold standard for treatment of Parkinson disease (PD) is levodopa/carbidopa (L/C), but long-term treatment frequently results in motor complications, such as wearing-off and motor fluctuations (eg, dyskinesia, \"on-off\" phenomenon). Istradefylline is a new drug with a unique pharmacologic profile that was approved by the FDA for use as adjunctive treatment to L/C in adult patients with PD experiencing \"off\" episodes. The drug was shown to reduce \"off\" time in 4 randomized, double-blind, placebo-controlled studies. The most common adverse effects are dyskinesia, dizziness, constipation, nausea, hallucinations, and insomnia. Unlike many drugs that treat PD, istradefylline is a nondopaminergic drug that exerts its effects via adenosine A2A receptor antagonism. The major drug interactions involve inhibitors or inducers of CYP3A4 as well as tobacco smoking via induction of CYP1A1. Istradefylline is taken once daily as a 20- or 40-mg dose, except in cases involving drug interactions or hepatic impairment. The cost of the drug is relatively expensive, which has implications for Medicare and private insurance coverage. Istradefylline is an alternative option to dopaminergic drugs such as dopamine agonists, monoamine oxidase B inhibitors, and catechol-O-methyltransferase inhibitors as an adjunct to L/C in patients with motor fluctuations, but clinical use will further define its role in treatment of PD.</p>","PeriodicalId":22710,"journal":{"name":"The Mental Health Clinician","volume":"12 1","pages":"32-36"},"PeriodicalIF":0.0000,"publicationDate":"2022-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/02/5a/i2168-9709-12-1-32.PMC8788305.pdf","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Mental Health Clinician","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9740/mhc.2022.01.032","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
Abstract
The current gold standard for treatment of Parkinson disease (PD) is levodopa/carbidopa (L/C), but long-term treatment frequently results in motor complications, such as wearing-off and motor fluctuations (eg, dyskinesia, "on-off" phenomenon). Istradefylline is a new drug with a unique pharmacologic profile that was approved by the FDA for use as adjunctive treatment to L/C in adult patients with PD experiencing "off" episodes. The drug was shown to reduce "off" time in 4 randomized, double-blind, placebo-controlled studies. The most common adverse effects are dyskinesia, dizziness, constipation, nausea, hallucinations, and insomnia. Unlike many drugs that treat PD, istradefylline is a nondopaminergic drug that exerts its effects via adenosine A2A receptor antagonism. The major drug interactions involve inhibitors or inducers of CYP3A4 as well as tobacco smoking via induction of CYP1A1. Istradefylline is taken once daily as a 20- or 40-mg dose, except in cases involving drug interactions or hepatic impairment. The cost of the drug is relatively expensive, which has implications for Medicare and private insurance coverage. Istradefylline is an alternative option to dopaminergic drugs such as dopamine agonists, monoamine oxidase B inhibitors, and catechol-O-methyltransferase inhibitors as an adjunct to L/C in patients with motor fluctuations, but clinical use will further define its role in treatment of PD.
目前治疗帕金森病(PD)的金标准是左旋多巴/卡比多巴(L/C),但长期治疗经常会导致运动并发症,如消退和运动波动(如运动障碍,“开-关”现象)。Istradefylline是一种具有独特药理学特征的新药,已被FDA批准用于成年PD“off”发作患者的L/C辅助治疗。在4项随机、双盲、安慰剂对照的研究中,该药物被证明可以缩短“停药”时间。最常见的副作用是运动障碍、头晕、便秘、恶心、幻觉和失眠。与许多治疗帕金森病的药物不同,iststradefylline是一种非多巴胺能药物,通过腺苷A2A受体拮抗剂发挥作用。主要的药物相互作用包括CYP3A4的抑制剂或诱导剂以及通过诱导CYP1A1吸烟。除涉及药物相互作用或肝损害的病例外,每日服用一次,剂量为20或40毫克。该药的成本相对昂贵,这对医疗保险和私人保险的覆盖范围有影响。isstradefylline是多巴胺能药物(如多巴胺激动剂、单胺氧化酶B抑制剂和儿茶酚- o -甲基转移酶抑制剂)的替代选择,可作为运动波动患者L/C的辅助药物,但临床使用将进一步确定其在PD治疗中的作用。