A review of disease progression models of Parkinson's disease and applications in clinical trials

被引:46
作者
Venuto, Charles S. [1 ,2 ]
Potter, Nicholas B. [1 ]
Dorsey, E. Ray [1 ,2 ]
Kieburtz, Karl [1 ,2 ]
机构
[1] Univ Rochester, Ctr Human Expt Therapeut, Rochester, NY USA
[2] Univ Rochester, Dept Neurol, Rochester, NY USA
关键词
Parkinson's disease; disease progression; pharmacometrics; disease model; UPDRS; MOTOR IMPAIRMENT; NATURAL-HISTORY; LEVODOPA; SELEGILINE; DECLINE; DESIGN; SYSTEM; SLOWS;
D O I
10.1002/mds.26644
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Quantitative disease progression models for neurodegenerative disorders are gaining recognition as important tools for drug development and evaluation. In Parkinson's disease (PD), several models have described longitudinal changes in the Unified Parkinson's Disease Rating Scale (UPDRS), one of the most utilized outcome measures for PD trials assessing disease progression. We conducted a literature review to examine the methods and applications of quantitative disease progression modeling for PD using a combination of key words including Parkinson disease, progression, and model. For this review, we focused on models of PD progression quantifying changes in the total UPDRS scores against time. Four different models reporting equations and parameters have been published using linear and nonlinear functions. The reasons for constructing disease progression models of PD thus far have been to quantify disease trajectories of PD patients in active and inactive treatment arms of clinical trials, to quantify and discern symptomatic and disease-modifying treatment effects, and to demonstrate how model-based methods may be used to design clinical trials. The historical lack of efficiency of PD clinical trials begs for model-based simulations in planning for studies that result in more informative conclusions, particularly around disease modification. (c) 2016 International Parkinson and Movement Disorder Society
引用
收藏
页码:947 / 956
页数:10
相关论文
共 64 条
[11]   Novel Methods and Technologies for 21st-Century Clinical Trials A Review [J].
Dorsey, E. Ray ;
Venuto, Charles ;
Venkataraman, Vinayak ;
Harris, Denzil A. ;
Kieburtz, Karl .
JAMA NEUROLOGY, 2015, 72 (05) :582-588
[12]   Design innovations and baseline findings in a long-term Parkinson's trial: The national institute of neurological disorders and stroke exploratory trials in Parkinson's Disease Long-Term Study-1 [J].
Elm, Jordan J. .
MOVEMENT DISORDERS, 2012, 27 (12) :1513-1521
[13]  
EMA, 2013, QUAL OP NOV DAT DRIV
[14]  
Fahn S, 2004, NEW ENGL J MED, V351, P2498
[15]  
Food and Drug Administration Center for Drug Evaluation Research, 2012, GUID IND ENR STRAT C
[16]  
Forys U., 2003, International Journal of Applied Mathematics and Computer Science, V13, P317
[17]   PROGRESSION OF PARKINSONS-DISEASE WITHOUT LEVODOPA [J].
GOETZ, CG ;
TANNER, CM ;
SHANNON, KM .
NEUROLOGY, 1987, 37 (04) :695-698
[18]   Placebo-associated improvements in motor function: Comparison of subjective and objective sections of the UPDRS in early Parkinson's disease [J].
Goetz, CG ;
Leurgans, S ;
Raman, R .
MOVEMENT DISORDERS, 2002, 17 (02) :283-288
[19]  
Goetz CG, 2000, MOVEMENT DISORD, V15, P479, DOI 10.1002/1531-8257(200005)15:3<479::AID-MDS1009>3.0.CO
[20]  
2-P