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Rapid onset of ulcerative colitis after treatment with interferon β1a in a patient with multiple sclerosis.
J Crohns Colitis. 2011 Feb;5(1):75-6. doi: 10.1016/j.crohns.2010.10.007. Epub 2010 Nov 26.
2
IFNβ-1b may severely exacerbate Japanese optic-spinal MS in neuromyelitis optica spectrum.干扰素-β-1b 可能会严重恶化视神经脊髓炎谱系疾病中的日本视神经脊髓炎。
Neurology. 2010 Oct 19;75(16):1423-7. doi: 10.1212/WNL.0b013e3181f8832e. Epub 2010 Sep 8.
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Anti-double stranded DNA and lupus syndrome induced by interferon-beta therapy in a patient with multiple sclerosis.一名多发性硬化症患者接受β-干扰素治疗后出现抗双链DNA及狼疮综合征
Lupus. 2009 Jan;18(1):78-80. doi: 10.1177/0961203308093550.
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Severe dermatomyositis triggered by interferon beta-1a therapy and associated with enhanced type I interferon signaling.由β-1a干扰素治疗引发并与I型干扰素信号增强相关的严重皮肌炎。
Arch Dermatol. 2008 Oct;144(10):1341-9. doi: 10.1001/archderm.144.10.1341.
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Interferon-beta treatment for multiple sclerosis.β-干扰素治疗多发性硬化症。
Neurotherapeutics. 2007 Oct;4(4):633-46. doi: 10.1016/j.nurt.2007.07.001.
6
Multiple sclerosis in Isfahan, Iran.伊朗伊斯法罕的多发性硬化症
Int Rev Neurobiol. 2007;79:357-75. doi: 10.1016/S0074-7742(07)79016-5.
7
Beneficial effect of interferon-beta treatment in patients with multiple sclerosis is associated with transient increase in serum IL-6 level in response to interferon-beta injection.干扰素-β治疗对多发性硬化症患者的有益作用与注射干扰素-β后血清IL-6水平的短暂升高有关。
Cytokine. 2006 Oct;36(1-2):69-74. doi: 10.1016/j.cyto.2006.10.013. Epub 2006 Dec 11.
8
Interferon beta-1b exacerbates multiple sclerosis with severe optic nerve and spinal cord demyelination.干扰素β-1b会加重伴有严重视神经和脊髓脱髓鞘的多发性硬化症。
J Neurol Sci. 2007 Jan 15;252(1):57-61. doi: 10.1016/j.jns.2006.10.008. Epub 2006 Nov 27.
9
Revised diagnostic criteria for neuromyelitis optica.视神经脊髓炎修订诊断标准。
Neurology. 2006 May 23;66(10):1485-9. doi: 10.1212/01.wnl.0000216139.44259.74.
10
Biological responsiveness to first injections of interferon-beta in patients with multiple sclerosis.多发性硬化症患者首次注射β-干扰素后的生物学反应。
J Neuroimmunol. 2005 Jan;158(1-2):195-203. doi: 10.1016/j.jneuroim.2004.08.006.

干扰素-β开始使用后多发性硬化症的快速恶化:9例报告。

Rapid exacerbation of multiple sclerosis following the initiation of interferon-β: report of nine cases.

作者信息

Etemadifar Masoud, Sarrami Amir Hossein

机构信息

Professor, Department of Neurology, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

J Res Med Sci. 2011 Dec;16(12):1619-22.

PMID:22973372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3434905/
Abstract

BACKGROUND

Interferon-β (IFN-β) is an effective drug in multiple sclerosis (MS) but it may cause acute exacerbation of MS following the initiation of treatment. This study evaluated patients with rapid exacerbation of multiple sclerosis (REMS) following the initiation of IFN-β.

METHODS

We retrospectively reviewed the clinical records of 2350 patients with multiple sclerosis who started treatment with IFN-β and were registered with Isfahan MS Society (IMSS). Patients with rapid exacerbation of multiple sclerosis within 24 hours after initiation of IFN-β treatment were selected and their demographic and clinical data were extracted.

RESULTS

We identified nine patients with rapid exacerbation of multiple sclerosis following the initiation of IFN-β. Their mean age at the time of treatment with IFN-β was 37.3 ± 6.28 years. Seven patients had rapid exacerbation of multiple sclerosis after initiation of IFN-β 1a and two patients after IFN-β 1b. The course of disease in all of these patients was relapsing-remitting. However, all had converted into secondary progression within the first year after occurrence of rapid exacerbation of multiple sclerosis following the initiation of IFN-β.

CONCLUSIONS

This study may indicate that the effects of IFN-β are not purely anti-inflammatory and a small percentage of MS patients experience rapid exacerbation of multiple sclerosis following the initiation of IFN-β. Future studies are needed to validate our findings.

摘要

背景

干扰素-β(IFN-β)是治疗多发性硬化症(MS)的一种有效药物,但在治疗开始后可能会导致MS急性加重。本研究评估了IFN-β治疗开始后出现多发性硬化症快速加重(REMS)的患者。

方法

我们回顾性分析了2350例开始接受IFN-β治疗并在伊斯法罕MS协会(IMSS)登记的多发性硬化症患者的临床记录。选择IFN-β治疗开始后24小时内出现多发性硬化症快速加重的患者,并提取他们的人口统计学和临床数据。

结果

我们确定了9例IFN-β治疗开始后出现多发性硬化症快速加重的患者。他们接受IFN-β治疗时的平均年龄为37.3±6.28岁。7例患者在开始使用IFN-β 1a后出现多发性硬化症快速加重,2例在使用IFN-β 1b后出现。所有这些患者的病程均为复发缓解型。然而,在IFN-β治疗开始后出现多发性硬化症快速加重后的第一年内,所有患者均转变为继发进展型。

结论

本研究可能表明IFN-β的作用并非单纯抗炎,一小部分MS患者在IFN-β治疗开始后会出现多发性硬化症快速加重。需要进一步的研究来验证我们的发现。