Gadolinium-enhancing or active T2 magnetic resonance imaging lesions in multiple sclerosis clinical trials?

被引:13
作者
Bonzano, L. [1 ,2 ]
Roccatagliata, L. [1 ,2 ]
Mancardi, G. L. [1 ,2 ]
Sormani, M. P. [3 ]
机构
[1] Univ Genoa, Dept Neurosci Ophthalmol & Genet, Genoa, Italy
[2] Univ Genoa, Magnet Resonance Res Ctr Nervous Syst Dis, Genoa, Italy
[3] Univ Genoa, Dept Hlth Sci, Biostat Unit, Genoa, Italy
关键词
clinical trial; gadolinium; magnetic resonance; meta-analysis; multiple sclerosis; randomized controlled trial; relapsing-remitting multiple sclerosis; DISEASE-ACTIVITY; DOUBLE-BLIND; MRI; MULTICENTER; EFFICACY; SAFETY; IMAGES;
D O I
10.1177/1352458509106610
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Background The treatment effects in multiple sclerosis (MS) clinical trials are often estimated by monitoring disease activity by the count of "active" plaques on T2-weighted or gadolinium (Gd)-enhanced T1-weighted magnetic resonance imaging (MRI). Objective To evaluate the relationship between the treatment effects estimated on T2-weighted or Gd-enhanced T1-weighted MRI. Methods Data were extracted from published randomized clinical trials in relapsing-remitting MS with frequent MRI, reporting both active T2 and Gd-enhancing lesions. A regression analysis was performed between the treatment effects estimated on the two different MRI endpoints. Results A strong association was found between the treatment effect on Gd-enhancing lesions and on active T2 lesions (R-2 = 0.93), and the treatment effect estimates were almost the same (slope = 0.96). Conclusion Defining either active T2 or Gd-enhancing lesions as MRI endpoint seems to be not crucial for monitoring MRI activity in MS clinical trials. The choice of the best MRI endpoint should be based on different considerations (e. g., sensitivity, reproducibility, time for assessment, safety, and patients' comfort). Further monitoring active T2 lesions could allow less expensive trials, without requiring injection of Gd-based contrast agents. Multiple Sclerosis 2009; 15: 1043-1047. http://msj.sagepub.com
引用
收藏
页码:1043 / 1047
页数:5
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