Istradefylline: A novel agent in the treatment of "off" episodes associated with levodopa/carbidopa use in Parkinson disease.

The Mental Health Clinician Pub Date : 2022-01-21 eCollection Date: 2022-01-01 DOI:10.9740/mhc.2022.01.032
Lauren Cummins, Marshall E Cates
{"title":"Istradefylline: A novel agent in the treatment of \"off\" episodes associated with levodopa/carbidopa use in Parkinson disease.","authors":"Lauren Cummins,&nbsp;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.

iststradefylline:一种治疗帕金森病患者左旋多巴/卡比多巴相关的“off”发作的新药物。
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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信