The effect of interferon beta-1b treatment on MRI measures of cerebral atrophy in secondary progressive multiple sclerosis

被引:195
|
作者
Molyneux, PD [1 ]
Kappos, L [1 ]
Polman, C [1 ]
Pozzilli, C [1 ]
Barkhof, F [1 ]
Filippi, M [1 ]
Yousry, T [1 ]
Hahn, D [1 ]
Wagner, K [1 ]
Ghazi, M [1 ]
Beckmann, K [1 ]
Dahlke, F [1 ]
Losseff, N [1 ]
Barker, GJ [1 ]
Thompson, AJ [1 ]
Miller, DH [1 ]
机构
[1] UCL Inst Neurol, Natl Hosp, NMR Res Unit, London WC1N 3BG, England
关键词
cerebral atrophy; interferon beta-1b; secondary progressive multiple sclerosis; multiple sclerosis; MRI;
D O I
10.1093/brain/123.11.2256
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The recently completed European trial of interferon beta-1b (IFN beta -1b) in patients with secondary progressive multiple sclerosis (SP multiple sclerosis) has given an opportunity to assess the impact of treatment on cerebral atrophy using serial MRI. Unenhanced T(1)-weighted brain imaging was acquired in a subgroup of 95 patients from five of the European centres; imaging was performed at 6-month intervals from month 0 to month 36. A blinded observer measured cerebral volume on four contiguous 5 mm cerebral hemisphere slices at each time point, using an algorithm with a high level of reproducibility and automation. There was a significant and progressive reduction in cerebral volume in both placebo and treated groups, with a mean reduction of 3.9 and 2.9%, respectively, by month 36 (P = 0.34 between groups). Exploratory subgroup analyses indicated that patients without gadolinium (Gd) enhancement at the baseline had a greater reduction of cerebral volume in the placebo group (mean reduction at month 36: placebo 5.1%, IFN beta -1b 1.8%, P < 0.05) whereas those with Gd-enhancing lesions showed a trend to greater reduction of cerebral volume if the patient was on IFN<beta>-1b (placebo 2.6%, IFN beta -1b, 3.7%; P > 0.05). These results are consistent with ongoing tissue loss in both arms of this study of secondary progressive multiple sclerosis. This finding is concordant with previous observations that disease progression, although delayed, is not halted by IFN beta. The different pattern seen in patients with and without baseline gadolinium enhancement suggests that part of the cerebral volume reduction observed in IFN beta -treated patients may be due to the anti-inflammatory/antioedematous effect of the drug. Longer periods of observation and larger groups of patients may be needed to detect the effects of treatment on cerebral atrophy in this population of patients with advanced disease.
引用
收藏
页码:2256 / 2263
页数:8
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