MRI results from the European Study on Intravenous Immunoglobulin in Secondary Progressive Multiple Sclerosis (ESIMS)

被引:36
作者
Fazekas, F
Sorensen, PS
Filippi, M
Ropele, S
Lin, X
Koelmel, HW
Fernandez, O
Pozzilli, C
O'Connor, P
Enriquez, MM
Hommes, OR
机构
[1] Med Univ Graz, Dept Neurol, A-8036 Graz, Austria
[2] Med Univ Graz, Dept Neuroradiol, Graz, Austria
[3] Copenhagen Univ Hosp, Rigshosp, Dept Neurol, Copenhagen, Denmark
[4] Ist Sci San Raffaele, Neuroimaging Res Unit, I-20132 Milan, Italy
[5] Ist Sci San Raffaele, Dept Neurol, I-20132 Milan, Italy
[6] Univ Osped San Raffaele, Milan, Italy
[7] Queens Med Ctr, Nottingham NG7 2UH, England
[8] Klinikum Erfurt, Dept Neurol, Erfurt, Germany
[9] Hosp Reg Carlos Haya, Dept Neurol, Malaga, Spain
[10] Univ Roma La Sapienza, Clin Neurol 1, Rome, Italy
[11] St Michaels Hosp, Toronto, ON M5B 1W8, Canada
[12] Bayer Vital, Leverkusen, Germany
[13] European Charcot Fdn, Nijmegen, Netherlands
关键词
brain atrophy; contrast enhancement; intravenous immunoglobulin; lesion load; magnetic resonance imaging; secondary progressive MS; treatment trial;
D O I
10.1191/1352458505ms1196oa
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background. Monthly application of high-dose intravenous immunoglobulin (IVIG) to patients with secondary progressive multiple sclerosis (MS) showed no clinical benefit in the European Study on Immunoglobulin in MS (ESIMS). Magnetic resonance imaging (MRI) results may provide insights into the morphologic consequences of such treatment. Methods: A total of 318 patients (mean age 44 +/- 7 years) were enrolled in 31 European and Canadian centres and treated monthly with 1 g/kg body weight of IVIG or equivalent amounts of albumin 0.1% for 27 months. MRI was performed at baseline and after 12 and 24 months and comprised of conventional dual-echo T2-weighted and T1-weighted scans before and after application of 0.1 mmol/kg Gd-DTPA. Results: Similar to clinical variables, MRI measures at baseline were well comparable between treatment groups except for a somewhat lower mean number of contrast-enhancing lesions and number of active scans in IVIG-treated patients. Over the trial period there was almost no change of the T2-lesion load and the 'black hole'volume in both treatment groups and the cumulative number of contrast-enhancing lesions were similar. There was only a trend for fewer new or enlarged T2-lesions in IVIG patients, which disappeared after correction for the imbalance in the number of contrast-enhancing lesions at baseline. Brain volume in terms of a partial cerebral fraction decreased significantly less with IVIG than placebo treatment (final visit. -0.62 +/- 0.88% versus -0.88 +/- 0.91%, P=0.009). This difference remained statistically significant with correction for active lesions at baseline (P=0.02) and was seen primarily in male patients and those with an Expanded Disability Status Scale score >= 6 and no relapses in the two years before the study. Conclusion: The absence of significant differences in conventional MRI measures between both treatment groups parallels the negative clinical results of ESIMS. The causes for and possible long-term clinical effects of a lower rate of brain volume loss in IVIG patients should be explored further.
引用
收藏
页码:433 / 440
页数:8
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