L-DOPA-INDUCED DYSKINESIA-CLINICAL PRESENTATION, GENETICS, AND TREATMENT

被引:44
作者
Prashanth, L. K. [1 ,2 ]
Fox, Susan [1 ,2 ]
Meissner, Wassilios G. [3 ,4 ,5 ]
机构
[1] Univ Toronto, Toronto Western Hosp, Morton & Gloria Shulman Movement Disorders Ctr, Toronto, ON M5V 2S8, Canada
[2] Univ Toronto, Toronto Western Hosp, Div Neurol, Toronto, ON M5V 2S8, Canada
[3] Univ Hosp Bordeaux, Dept Neurol, F-33076 Bordeaux, France
[4] Univ Hosp Bordeaux, French Reference Ctr MSA, F-33076 Bordeaux, France
[5] Univ Bordeaux 2, CNRS, Inst Neurodegenerat Dis, UMR 5293, F-33076 Bordeaux, France
来源
PATHOPHYSIOLOGY, PHARMACOLOGY, AND BIOCHEMISTRY OF DYSKINESIA | 2011年 / 98卷
关键词
LEVODOPA-INDUCED DYSKINESIAS; ADVANCED PARKINSONS-DISEASE; CLOZAPINE IMPROVES DYSKINESIAS; PEAK-DOSE DYSKINESIAS; DOUBLE-BLIND; MOTOR FLUCTUATIONS; SUBCUTANEOUS APOMORPHINE; FOLLOW-UP; SYDNEY MULTICENTER; AMANTADINE;
D O I
10.1016/B978-0-12-381328-2.00002-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Levodopa-induced dyskinesia (LID) has been recognized since the introduction of levodopa for the management of Parkinson's disease (PD) and continues to be one of the most clinically challenging factors in long-term management of patients with PD. Most patients develop LID within 10 years of PD onset and the cause has been attributed to various factors including disease demographics, pharmacological, and possibly genetic causes. The clinical pattern of LID varies and shows intra and inter-patient variability and has been classified based upon phenomenology and relation to timing of levodopa. The potential armamentarium to address and manage LID has significantly increased in the last decade. This chapter addresses the current understanding of various clinical aspects and available therapeutics for LID.
引用
收藏
页码:31 / 54
页数:24
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