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推断帕金森病患者对左旋多巴的长期反应。

Inferring the long duration response to levodopa in Parkinson's disease.

机构信息

Neurosciences Department, Monash Medical Centre, 246 Clayton Road, Clayton, Victoria, 3168, Australia.

Neurosciences Department, Monash Medical Centre, 246 Clayton Road, Clayton, Victoria, 3168, Australia.

出版信息

Parkinsonism Relat Disord. 2019 Mar;60:133-137. doi: 10.1016/j.parkreldis.2018.09.002. Epub 2018 Sep 6.

Abstract

INTRODUCTION

The long duration response to levodopa in Parkinson's disease outlasts drug elimination by days to weeks. Though a substantive part of anti-parkinsonian motor benefit, it cannot easily be observed.

OBJECTIVES

To infer the magnitude of the long duration response during the first decade of Parkinson's disease and identify factors that influence it.

METHODS

Serial practically defined off scores of 24 patients from a longitudinal study of levodopa short duration response were used to establish their rate of motor progression. A line of notional untreated disability (as if drug treatment had never been given) with the same progression gradient was the basis for calculation of the long duration response. Predictors of mean long duration response amplitude were identified using a multiple linear regression model.

RESULTS

Over a mean treatment period of 16.6 ± 4.4 years, annual increase in motor disability was 2.3% of the maximum score. The long duration response composed 49% of total levodopa response during the first decade of treatment, and this proportion was significantly higher soon after commencing levodopa (p = 0.001). Higher pre-treatment motor score (r = 0.60) and lower MMSE (r = 0.60) were the main predictors of a larger long duration response. There was little correlation between long and short duration responses.

CONCLUSIONS

Long duration responses contribute almost half of the total levodopa benefit during the first decade of treatment. An appreciation of both long and short duration components of drug symptomatic effects is important in clinical trial design to investigate possible neuroprotective treatments.

摘要

简介

帕金森病患者对左旋多巴的长期反应持续时间超过药物消除时间数天至数周。尽管这是抗帕金森运动症状的重要部分,但却难以观察到。

目的

推断帕金森病早期左旋多巴长期反应的幅度,并确定影响其的因素。

方法

使用来自左旋多巴短期反应纵向研究的 24 名患者的连续实际定义的关闭评分,来确定他们的运动进展速度。一条无药物治疗的假设性失能线(就像从未给予药物治疗一样),具有相同的进展梯度,是计算长期反应的基础。使用多元线性回归模型确定平均长期反应幅度的预测因子。

结果

在平均治疗期间为 16.6±4.4 年期间,运动障碍的年增长率为最大评分的 2.3%。在治疗的前十年中,长期反应构成了左旋多巴总反应的 49%,并且在开始使用左旋多巴后不久,这一比例显著更高(p=0.001)。较高的治疗前运动评分(r=0.60)和较低的 MMSE(r=0.60)是较大长期反应的主要预测因子。长期和短期反应之间相关性较小。

结论

长期反应在治疗的前十年中几乎占左旋多巴总获益的一半。在临床试验设计中,了解药物症状效应的长期和短期成分对于研究可能的神经保护治疗非常重要。

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