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在帕金森病患者的药物治疗中加入儿茶酚-O-甲基转移酶抑制剂是否有益?系统评价。

Are There Benefits in Adding Catechol-O Methyltransferase Inhibitors in the Pharmacotherapy of Parkinson's Disease Patients? A Systematic Review.

机构信息

Current Medical Student, Lancaster Medical School, Lancaster, UK.

Consultant Neurologist, Lancashire Teaching Hospitals NHS Foundation Trust, Preston, UK.

出版信息

J Parkinsons Dis. 2018;8(2):217-231. doi: 10.3233/JPD-171225.

Abstract

BACKGROUND

A qualified consensus suggests that a combination of levodopa with a peripherally acting dopa decarboxylase inhibitor continues to present the gold standard treatment of Parkinson's disease (PD). However, as the disease progresses the therapeutic window of levodopa becomes narrowed. Pharmacological strategies for motor fluctuations are focused on providing less pulsatile and more continuous dopaminergic stimulation. Peripheral catechol-O-methyltransferase (COMT) inhibition improves the bioavailability of levodopa and results in a prolonged response.

OBJECTIVE

The primary aim of this study was to investigate the efficacy and safety of the two available COMT inhibitors; entacapone and tolcapone and the recently introduced opicapone.

METHODS

Electronic databases were systematically searched for original studies published within the last 37 years. In addition, lists of identified studies, reviews and their references were examined.

RESULTS

Twelve studies fulfilled the inclusion criteria. 3701 patients with PD were included in this systematic review.

CONCLUSIONS

Adjuvant treatment of PD patients experiencing motor fluctuations with entacapone resulted in improvement of motor function and was well tolerated. Therefore, entacapone presented an acceptable benefit to risk ratio. Tolcapone appeared to result in a greater therapeutic effect. However, this was not consistent across all motor variables and studies, and thus would not support its use, given the current onerous monitoring that is required. Opicapone was not associated with adverse reactions in a phase III trial but did not present a greater efficacy than entacapone, and thus further studies are required in order to illustrate its cost effectiveness.

摘要

背景

一项合格的共识表明,左旋多巴与外周作用的多巴脱羧酶抑制剂联合使用仍然是治疗帕金森病(PD)的金标准。然而,随着疾病的进展,左旋多巴的治疗窗口变窄。针对运动波动的药物治疗策略集中在提供较少脉冲和更持续的多巴胺能刺激。外周儿茶酚-O-甲基转移酶(COMT)抑制可提高左旋多巴的生物利用度,从而延长其反应时间。

目的

本研究的主要目的是研究两种可用的 COMT 抑制剂(恩他卡朋和托卡朋)和最近推出的奥匹卡朋的疗效和安全性。

方法

系统地检索了过去 37 年内发表的原始研究。此外,还检查了已确定研究、综述及其参考文献的列表。

结果

有 12 项研究符合纳入标准。共有 3701 例 PD 患者纳入本系统评价。

结论

在出现运动波动的 PD 患者中,使用恩他卡朋作为辅助治疗可改善运动功能且具有良好的耐受性。因此,恩他卡朋具有可接受的获益-风险比。托卡朋似乎具有更大的治疗效果。然而,并非所有运动变量和研究都如此,因此,鉴于目前需要进行严格的监测,不支持其使用。奥匹卡朋在 III 期试验中未与不良反应相关,但与恩他卡朋相比并未显示出更大的疗效,因此需要进一步的研究来阐明其成本效益。

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