Emerging drugs for the treatment of L-DOPA-induced dyskinesia: an update

被引:12
作者
AlShimemeri, Sohaila [1 ,2 ,3 ]
Fox, Susan H. [1 ,2 ]
Visanji, Naomi P. [1 ,2 ]
机构
[1] Toronto Western Hosp, Edmond J Safra Program Parkinson Dis, 399 Bathurst St, Toronto, ON M5T 2S8, Canada
[2] Toronto Western Hosp, Morton & Gloria Shulman Movement Disorders Ctr, 399 Bathurst St, Toronto, ON M5T 2S8, Canada
[3] King Saud Univ, Div Neurol, Dept Med, Riyadh, Saudi Arabia
关键词
Parkinson's disease; L-DOPA-induced dyskinesia; dopamine; glutamate; serotonin; LEVODOPA-INDUCED DYSKINESIA; QUALITY-OF-LIFE; DEEP BRAIN-STIMULATION; 1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE-LESIONED MACAQUE MODEL; ALLOSTERIC MODULATOR DIPRAGLURANT; 5-HT1A RECEPTOR ACTIVATION; EARLY PARKINSONS-DISEASE; DELAYED-START TRIAL; DOUBLE-BLIND; MOTOR COMPLICATIONS;
D O I
10.1080/14728214.2020.1763954
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Prolonged treatment with L-3,4-dihydroxyphenylalanine (L-DOPA) leads to the development of uncontrolled movements (L-DOPA-induced dyskinesias (LID)) in Parkinson's disease (PD). There is currently only a single approved drug for the treatment of LID, a long-acting preparation of the NMDA antagonist, amantadine, that has variable benefits and side-effects. Therefore, new treatments for LID remain an unmet in PD. Areas covered: We review the current strategies for the management of LID; the pathogenic mechanisms underlying the development of LID, which provides the rationale for clinical trials of novel targets for LID and provide a review of phase II/III trials for emerging drugs for LID, with either positive results, or ongoing studies, reported between January 2014 and December 2019. Expert opinion: There are several ongoing studies for agents that showed possible benefit at phase Ib/IIa for reducing LID. However, there are no new positive phase III double-blind randomized controlled clinical trials (DBRCT) for emerging treatments for LID. Generating better preclinical models, more precise recruitment tools and better outcome measures remain a priority. The pharmacology of drugs investigated for LID may be too selective; therefore, evaluating combinations of drugs is worthy of consideration as is the repurposing of existing drugs with multiple pharmacological targets.
引用
收藏
页码:131 / 144
页数:14
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