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新发帕金森病的急性多巴反应性评价
引用本文:冯涛,芦林龙,张璇,李伟,于学英,杨雅琴,王拥军. 新发帕金森病的急性多巴反应性评价[J]. 中国临床神经科学, 2009, 17(4): 377-380
作者姓名:冯涛  芦林龙  张璇  李伟  于学英  杨雅琴  王拥军
作者单位:首都医科大学附属北京天坛医院神经内科,100050
摘    要:目的:建立急性左旋多巴负荷试验用于鉴别新发帕金森病(PD)与新发帕金森综合征(PDS)患者,并筛选评价指标的临界值。方法:选择89例有PD样表现但未服用过左旋多巴的患者,根据临床诊断分为PD组(n=48)和PDS组(n=41),进行了急性左旋多巴/卡比多巴(100/25mg)试验。根据两组患者统-PD评分运动分量表(UPDRS—Ⅲ)评分的平均最大改善率进行比较,并建立受试者工作特征(ROC)曲线,以该曲线上最大Youden指数对应的运动评分最大改善率作为临界值。结果:PD组在服用左旋多巴-卡比多巴后的平均UPDRS-Ⅲ评分平均最大改善率高于PDS组,差异有统计学意义(P〈0.01)。建立的ROC曲线在鉴别PD和PDS差异具有统计学意义,ROC曲线下面积为0.827(P〈0.01),对应上网UPDRS运动评分改善率的最佳临界值为12.45%(Youden指数0.565,敏感度80.9%,特异度75.6%)。结论:急性左旋多巴-卡比多巴试验可作为PD疗效和诊断的一种辅助参考方法。

关 键 词:帕金森病  左旋多巴  帕金森综合征

Acute Tests with L-dopa-carbidopa in De novo Patients with Primary Parkinson's Disease FENG Tao,
FENG Tao,L U Lin-Long,ZHANG Xuan,Li Wei,YU Xue-Ying,YANG Ya-Qin,WANG Yong-Jun. Acute Tests with L-dopa-carbidopa in De novo Patients with Primary Parkinson's Disease FENG Tao,[J]. Chinese Journal of Clinical Neurosciences, 2009, 17(4): 377-380
Authors:FENG Tao  L U Lin-Long  ZHANG Xuan  Li Wei  YU Xue-Ying  YANG Ya-Qin  WANG Yong-Jun
Affiliation:(Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China)
Abstract:Aim: To establish a new type of acute test with L-dopa-carbidopa and evaluate its diagnostic value in de novo patients with primary Parkinson's disease(PD) and parkinsonism(PDS). Methods: 89 de novo patients were enrolled in this study, which include 48 patients with primary PD and 41 patients with PDS. The patients underwent the acute test with 100/25 mg of L-dopa-carbidopa. The peak UPDRS-III improvement after administration of L-dopa-carbidopa compared with the baseline was defined as motor response to L-dopa. The receiver operating characteristic(ROC) curves comparing the motor response of primary PD with that of non-PD were plotted. The points on ROC curves with maximal Youden index were defined as the optimal cutoff points. Results: The maximum UPDRS-Ⅲ improvement of de novo patients with PD was significantly higher than that of patients with PDS (19.15% ± 10.26% vs 8.63% ± 6.07%, P〈0.01). The area under the curve of ROC for the test was 0.827(P〈0.01). The optimal cutoff points for UPDRS-Ⅲ improvement was 12.45% (Youden index 0.565, sensitivity 80.9%, specificity 75.6%). Conclusion: This test of L-dopa-carbidopa can be used to evaluate L-dopa-responsiveness in patients with primary PD as an additional tool for clinical diagnoses of PD.
Keywords:Parkinson's disease  L-dopa  Parkinsonism
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