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作 者:Kay Cheong Teo Shu-Leong Ho
机构地区:[1]Division of Neurology,Department of Medicine,University of Hong Kong,Hong Kong,China [2]Research Centre of Heart,Brain,Hormone and Healthy Aging(HBHA),University of Hong Kong,Hong Kong,China
出 处:《Translational Neurodegeneration》2013年第1期124-133,共10页转化神经变性病(英文)
基 金:The authors’work is supported by the Henry G Leong Endowed Professorship;the Donation Fund for Neurology Research,University of Hong Kong.
摘 要:There is a substantial amount of evidence from experimental parkinsonian models to show the neuroprotective effects of monoamine oxidase-B(MAOB)inhibitors.They have been studied for their potential disease-modifying effects in Parkinson’s disease(PD)for over 20 years in various clinical trials.This review provides a summary of the clinical trials and discusses the implications of their results in the context of disease-modification in PD.Earlier clinical trials on selegiline were confounded by symptomatic effects of this drug.Later clinical trials on rasagiline using delayed-start design provide newer insights in disease-modification in PD but success in achieving the aims of this strategy remain elusive due to obstacles,some of which may be insurmountable.
关 键 词:Parkinson's disease Monoamine oxidase-B inhibitors Disease-modification Neuroprotection SELEGILINE RASAGILINE
分 类 号:R74[医药卫生—神经病学与精神病学]
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