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恩他卡朋抑制儿茶酚-O-甲基转移酶的临床优势——综述

Clinical advantages of COMT inhibition with entacapone - a review.

作者信息

Gordin A, Kaakkola S, Teräväinen H

机构信息

Research Centre, Orion Pharma, Espoo, Finland.

出版信息

J Neural Transm (Vienna). 2004 Oct;111(10-11):1343-63. doi: 10.1007/s00702-004-0190-3. Epub 2004 Aug 3.

Abstract

Two catechol- O-methyltransferase (COMT) inhibitors, entacapone and tolcapone, were developed during the 1990's to be used as adjuncts to levodopa (LD) - dopa decarboxylase (DDC) inhibitors in the treatment of Parkinson's disease (PD). Entacapone is currently in wide clinical use, while tolcapone can be used in restricted indications only, due to its hepatotoxicity. COMT inhibitors prolong the elimination of LD, while DDC inhibitors mainly increase its absorption; both mechanisms leading to increased bioavailability of LD. The pharmacokinetic properties of LD, carbidopa and entacapone are quite similar, and entacapone is administered concomitantly with LD plus carbidopa. Entacapone prolongs the clinical effect of each LD dose by 30 to 40 minutes; this effect is seen already after the first entacapone dose. When LD is administered in several frequent daily doses, addition of entacapone reduces the daily fluctuations of plasma LD by 30 to 40%. Based on studies with home diaries, entacapone increases the daily ON-time by an average of one to two hours, and reduces the daily OFF-time correspondingly in patients with PD with motor fluctuations. The daily LD dose has been reduced by 10 to 30%. These positive effects are sustained in long term use over several years. There is still scant information of the benefit of entacapone in patients without motor fluctuations. Entacapone can cause both dopaminergic and non-dopaminergic adverse events. Increased dyskinesias are most frequently recorded in patients with motor fluctuations. The dopaminergic adverse events can usually be diminished by reducing the LD dose. Non-dopaminergic adverse events are abdominal pain and diarrhea. Diarrhoea has led to discontinuation in 3 to 4% of the patients in clinical trials. Entacapone has not been connected to liver toxicity and there are no indications to follow laboratory safety during treatment. The benefit-risk ratio of entacapone is considered favorable.A triple LD/carbidopa/entacapone combination tablet has recently been developed. Three LD strengths (50, 100 and 150 mg) are available, each contains 200 mg of entacapone. The majority of the patients can be managed with these three LD strengths. Entacapone has today an established position in treatment of PD patients with motor fluctuations, either as a separate tablet or as the triple LD combination.

摘要

两种儿茶酚 - O - 甲基转移酶(COMT)抑制剂,恩他卡朋和托卡朋,是在20世纪90年代研发出来的,用作左旋多巴(LD) - 多巴脱羧酶(DDC)抑制剂的辅助药物,用于治疗帕金森病(PD)。恩他卡朋目前在临床上广泛使用,而托卡朋由于具有肝毒性,仅可用于特定适应症。COMT抑制剂可延长LD的消除时间,而DDC抑制剂主要增加其吸收;这两种机制均导致LD生物利用度增加。LD、卡比多巴和恩他卡朋的药代动力学特性非常相似,恩他卡朋与LD加卡比多巴同时给药。恩他卡朋可使每剂LD的临床效果延长30至40分钟;在首次服用恩他卡朋后即可观察到这种效果。当LD每日多次给药时,加用恩他卡朋可使血浆LD的每日波动降低30%至40%。根据家庭日记研究,恩他卡朋可使有运动波动的PD患者的每日“开”期平均增加1至2小时,并相应减少每日“关”期。每日LD剂量可减少10%至30%。这些积极效果在数年的长期使用中得以维持。关于恩他卡朋对无运动波动患者的益处,目前仍知之甚少。恩他卡朋可引起多巴胺能和非多巴胺能不良事件。运动波动患者中最常记录到异动症增加。多巴胺能不良事件通常可通过减少LD剂量来减轻。非多巴胺能不良事件为腹痛和腹泻。在临床试验中,腹泻导致3%至4%的患者停药。恩他卡朋与肝毒性无关,治疗期间无需监测实验室安全性指标。恩他卡朋的效益风险比被认为是有利的。最近研发出了一种LD/卡比多巴/恩他卡朋三联复方片剂。有三种LD规格(50、100和150毫克)可供选择,每种均含有200毫克恩他卡朋。大多数患者使用这三种LD规格即可得到治疗。如今,恩他卡朋在治疗有运动波动症状的PD患者中已确立了地位,既可以单独片剂形式使用,也可以制成LD三联复方制剂使用。

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