Disease progression and pharmacodynamics in Parkinson disease - Evidence for functional protection with levodopa and other treatments

被引:63
|
作者
Holford, Nicholas H. G. [1 ]
Chan, Phylinda L. S.
Nutt, John G.
Kieburtz, Karl
Shoulson, Ira
机构
[1] Univ Auckland, Dept Pharmacol & Clin Pharmacol, Auckland 1, New Zealand
[2] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97201 USA
[3] Dept Neurol, Rochester, NY USA
关键词
levodopa; deprenyl; bromocriptine; pergolide; pharmacodynamics; disease progression; Parkinson's disease;
D O I
10.1007/s10928-006-9012-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We have modelled the Unified Parkinson's Disease Rating Scale (UPDRS) scores collected in 800 subjects followed for 8 years. Newly diagnosed and previously untreated subjects were initially randomized to treatment with placebo, deprenyl, tocopherol or both and, when clinical disability required, received one or more dopaminergic agents (levodopa (carbidopa/levodopa), bromocriptine, or pergolide). Using models for disease progression and pharmacodynamic models for drug effects we have characterized the changes in UPDRS over time to determine the influence of the various drug treatments. We have confirmed and quantitated the relative symptomatic benefits of the dopaminergic agents and provide model-based evidence for slowing of disease progression.
引用
收藏
页码:281 / 311
页数:31
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