Department of Neurology, Medical University of Innsbruck, Austria.
Clin Interv Aging. 2010 Sep 7;5:229-38. doi: 10.2147/cia.s6456.
After more than 40 years of clinical use, levodopa (LD) remains the gold standard of symptomatic efficacy in the drug treatment of Parkinson's disease (PD). Compared with other available dopaminergic therapies, dopamine replacement with LD is associated with the greatest improvement in motor function. Long-term treatment with LD is, however, often complicated by the development of various types of motor response oscillations over the day, as well as drug-induced dyskinesias. Motor fluctuations can be improved by the addition of drugs such as entacapone or monoamine oxidase inhibitors, which extend the half-life of levodopa or dopamine, respectively. However, dyskinesia control still represents a major challenge. As a result, many neurologists have become cautious when prescribing therapy with LD. This review summarizes the available evidence regarding the use of LD to treat PD and will also address the issue of LD delivery as a critical factor for the drug's propensity to induce motor complications.
左旋多巴(LD)经过 40 多年的临床应用,仍然是治疗帕金森病(PD)药物治疗中症状疗效的金标准。与其他可用的多巴胺能疗法相比,用 LD 进行多巴胺替代与运动功能的最大改善相关。然而,长期使用 LD 通常会导致一天中出现各种类型的运动反应波动,以及药物引起的运动障碍。通过添加恩他卡朋或单胺氧化酶抑制剂等药物可以改善运动波动,这些药物分别延长了 LD 或多巴胺的半衰期。然而,运动障碍的控制仍然是一个主要挑战。因此,许多神经科医生在开具 LD 治疗处方时变得谨慎。本综述总结了有关使用 LD 治疗 PD 的现有证据,还将解决 LD 给药作为药物诱导运动并发症倾向的关键因素的问题。