Utility of the Mattis dementia rating scale to assess the efficacy of rivastigmine in dementia associated with Parkinson's disease

被引:20
作者
Dujardin, Kathy [1 ]
Devos, David
Duhem, Stephane
Destee, Alain
Marie, Rose-Marie
Durif, Franck
Lacomblez, Lucette
Touchon, Jacques
Pollak, Pierre
Pere, Jean-Jacques
机构
[1] CHU Lille, Hop Salengro, F-59037 Lille, France
[2] Fac Med, Neurol & Movement Disorders Unit, EA2683, Lille, France
[3] Lille Univ Hosp, Lille, France
[4] CHU Cote Nacre, Neurol Serv, Caen, France
[5] Hop Gabriel Montpied, Serv Neurol, Clermont Ferrand, France
[6] Hop La Pitie Salpetriere, Federat Neurol, Paris, France
[7] CHU Guy De Chauliac, Unite Neurol Comportementale & Degenerat, Montpellier, France
[8] CHU Grenoble, Neurol Serv, F-38043 Grenoble, France
关键词
cognitive dysfunction in PD; mattis dementia rating scale; dementia; cholinesterase inhibitors;
D O I
10.1007/s00415-006-0175-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction The severe, cortical, cholinergic depletion accompanying Parkinson's disease (PD) is considered as a highly probable correlate of cognitive and behavioural dysfunction. Recent studies have demonstrated that cholinesterase inhibitors (notably rivastigmine) are beneficial in patients suffering from dementia associated with PD (PDD). However, the primary efficacy variables used in such work came from scales designed for Alzheimer's disease (AD), even though the cognitive symptoms in PD and AD dementia do not overlap completely. The aim of the present study (a double-blind, placebo-controlled clinical trial) was to determine the utility of the Mattis dementia rating scale - the most commonly used scale in PD patients - to assess the efficacy of a 24-week rivastigmine treatment. Methods Twenty-eight patients with PD, who constituted a subgroup of patients enrolled to the EXPRESS study (Emre et al, N Engl J Med 2004) participated in this study. They suffered from mild to moderately severe dementia (MMSE scores above 10 and below 24), with an onset of cognitive symptoms occurring at least two years after the diagnosis of PD. Patients were randomly assigned to treatment with rivastigmine (3 to 12 mg per day) or placebo. The Mattis dementia rating scale was administered to patients from six centres in France at the baseline and end-point visits. Results Compared with placebo, a 24-week rivastigmine treatment led to a significant improvement in the overall score on the Mattis dementia rating scale (p = 0.031), with a trend towards a significant improvement in the "Attention" subscale score (p = 0.061). Correlation analysis showed that in the rivastigmine group, performance on the Mattis "Attention" and "Initiation" subscales appeared to contribute heavily to the improvement in the overall score. Moreover, the latter was also related to an improvement in activities of daily living and a reduction in behavioural disturbances. Discussion By using the Mattis dementia rating scale (which comprises items that are sensitive to executive dysfunction), the present study confirmed that rivastigmine has a beneficial effect on cognitive function in PDD. Despite our study's small sample size, the Mattis scale was able to detect this improvement and could thus be considered as an interesting outcome measure in further work.
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页码:1154 / 1159
页数:6
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