Simuni Tanya, Brundin Patrik
Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Laboratory for Translational Parkinson's Disease Research, Center for Neurodegenerative Science, Van Andel Research Institute, Grand Rapids, MI, USA Neuronal Survival Unit, Department of Experimental Medical Science, Wallenberg Neuroscience Center, Lund, Sweden.
J Parkinsons Dis. 2014;4(3):345-7. doi: 10.3233/JPD-149001.
A recent study by Aviles-Olmos and colleagues suggests that 12 months of treatment with the glucagon-like peptide-1 receptor agonist exenatide improves motor and cognitive symptoms in Parkinson's disease (PD), and that the effect persists as long as 12 months after termination of the treatment. Due to the lack of a placebo control, one cannot exclude that the observed differences between patients receiving daily injections of exenatide and non-treated controls are due to a placebo effect. We discuss that large group differences in two independent functional measures remain for at least 12 months following the cessation of exenatide treatment and that this warrants a double-blind placebo-controlled trial with exenatide in PD.
阿维莱斯 - 奥尔莫斯及其同事最近的一项研究表明,使用胰高血糖素样肽 -1受体激动剂艾塞那肽进行12个月的治疗可改善帕金森病(PD)的运动和认知症状,且该效果在治疗终止后长达12个月仍持续存在。由于缺乏安慰剂对照,无法排除每日注射艾塞那肽的患者与未治疗的对照组之间观察到的差异是由安慰剂效应导致的。我们讨论了在艾塞那肽治疗停止后,两项独立功能测量中的大组差异至少持续12个月,这使得有必要进行一项针对帕金森病患者使用艾塞那肽的双盲安慰剂对照试验。