Motor fluctuations due to interaction between dietary protein and levodopa in Parkinson's disease.

Journal of Clinical Movement Disorders Pub Date : 2016-05-26 eCollection Date: 2016-01-01 DOI:10.1186/s40734-016-0036-9
Tuhin Virmani, Sirinan Tazan, Pietro Mazzoni, Blair Ford, Paul E Greene
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引用次数: 36

Abstract

Background: The modulation of levodopa transport across the blood brain barrier by large neutral amino acids is well documented. Protein limitation and protein redistribution diets may improve motor fluctuations in patients with Parkinson's disease but the pharmacokinetics and pharmacodynamics of levodopa and amino acids are highly variable.

Methods: Clinical records of 1037 Parkinson's disease patients were analyzed to determine the proportion of patients with motor fluctuations related to protein interaction with levodopa. Motor fluctuations due to protein interaction with levodopa were defined as dietary protein being associated with (i) longer time to levodopa effectiveness, (ii) reduced benefit or duration of benefit, (iii) dose failures or (iv) earlier wearing off from a previously effective dose. Dose failures, sudden, painful or behavioral wearing-off periods, gait freezing, nausea, hallucinations, orthostasis, and dyskinesias were taken as markers of motor fluctuations, disease severity, and levodopa side effects potentially influenced by protein.

Results: 5.9 % of Parkinson's disease patients on levodopa, and 12.4 % with motor fluctuations on levodopa correlated their fluctuations with the relative timing of levodopa and protein intake. These patients were younger at disease onset, had worse motor fluctuations and had a higher incidence of family members with Parkinson's disease. Early wearing off or decreased dose efficacy were most commonly associated with protein interaction. 60 % of patients who modified their diets had weight loss.

Conclusions: This study suggests that clinically significant protein interaction with levodopa may occur mostly in a subset of Parkinson's disease patients with earlier disease onset and those with familial disease.

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帕金森病患者饮食蛋白与左旋多巴相互作用引起的运动波动。
背景:大的中性氨基酸调节左旋多巴在血脑屏障中的转运是有充分证据的。蛋白质限制和蛋白质再分配饮食可能改善帕金森病患者的运动波动,但左旋多巴和氨基酸的药代动力学和药效学是高度可变的。方法:对1037例帕金森病患者的临床资料进行分析,确定左旋多巴蛋白相互作用引起运动波动的患者比例。蛋白质与左旋多巴相互作用引起的运动波动被定义为膳食蛋白质与(i)左旋多巴生效时间较长,(ii)益处或益处持续时间减少,(iii)剂量失败或(iv)先前有效剂量较早消失有关。剂量失败、突然、疼痛或行为消退期、步态冻结、恶心、幻觉、直立和运动障碍被视为运动波动、疾病严重程度和可能受蛋白质影响的左旋多巴副作用的标志。结果:5.9%的帕金森病患者服用左旋多巴,12.4%的患者服用左旋多巴后出现运动波动,其波动与左旋多巴和蛋白质摄入的相对时间相关。这些患者发病时更年轻,运动波动更严重,家族成员患帕金森病的几率更高。早期药效消退或剂量效力降低最常与蛋白质相互作用有关。60%的患者在调整饮食后体重减轻。结论:本研究提示,与左旋多巴有临床意义的蛋白相互作用可能主要发生在发病较早的帕金森病患者和家族性疾病患者中。
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