Progress towards therapies for disease modification in Parkinson's disease

被引:220
|
作者
Vijiaratnam, Nirosen [1 ,2 ]
Simuni, Tanya [3 ]
Bandmann, Oliver [4 ]
Morris, Huw R. [1 ,2 ]
Foltynie, Thomas [1 ,2 ]
机构
[1] UCL Queen Sq Inst Neurol, Dept Clin & Movement Neurosci, London WC1N 3BG, England
[2] Natl Hosp Neurol & Neurosurg, Queen Sq, London, England
[3] Northwestern Univ, Feinberg Sch Med, Parkinsons Dis & Movement Disorders Ctr, Chicago, IL 60611 USA
[4] Univ Sheffield, Sheffield Inst Translat Neurosci, Sheffield, S Yorkshire, England
来源
LANCET NEUROLOGY | 2021年 / 20卷 / 07期
关键词
REDUCES ALPHA-SYNUCLEIN; LRRK2; KINASE-ACTIVITY; DELAYED-START TRIAL; CLINICAL-TRIAL; MYELOPEROXIDASE INHIBITOR; MITOCHONDRIAL DYSFUNCTION; MODIFYING THERAPY; ANIMAL-MODELS; DOUBLE-BLIND; MOUSE MODEL;
D O I
10.1016/S1474-4422(21)00061-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The development of interventions to slow or halt the progression of Parkinson's disease remains a priority for patients and researchers alike. To date, no agents have been shown to have unequivocal evidence of disease-modifying effects in Parkinson's disease. The absence of disease-modifying treatments might relate not only to inadequate approaches for the selection of therapeutic candidates but also to insufficient attention to detail in clinical trial design. Better understanding of Parkinson's disease pathogenesis associated with advances in laboratory models, the use of objective biomarkers of disease progression and target engagement, and a focus on agents known to be safe for human use, alongside the use of precision medicine approaches, should together greatly increase the likelihood for successful identification of disease-modifying treatments for Parkinson's disease.
引用
收藏
页码:559 / 572
页数:14
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