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预测复发缓解型多发性硬化症中β-干扰素治疗失败的情况。

Predicting beta-interferon failure in relapsing-remitting multiple sclerosis.

作者信息

O'Rourke K, Walsh C, Antonelli G, Hutchinson M

机构信息

Department of Neurology, St Vincent's University Hospital, Dublin, Ireland.

出版信息

Mult Scler. 2007 Apr;13(3):336-42. doi: 10.1177/1352458506071309. Epub 2007 Jan 29.

DOI:10.1177/1352458506071309
PMID:17439902
Abstract

Proposed beta-interferon (IFNbeta) treatment failure criteria for patients with relapsing-remitting multiple sclerosis (RRMS) have not been validated in clinical practice. This study aimed to establish (a) whether IFNbeta attenuated accumulation of fixed disability in comparison to a cohort of matched historical control subjects from the Sylvia Lawry centre for MS research, and (b) whether relapse-based treatment failure criteria or clinical and demographic variables had predictive value for the accumulation of fixed disability. Of the 175 IFNbeta-treated RRMS patients, 60 (34%) developed accumulation of fixed disability over a median of five years follow-up, which was significantly less than the rate of accumulation of fixed disability in the control group (P<0.0001). Any relapse in the treatment period predicted accumulation of fixed disability with a sensitivity of 80% and specificity of 43%; patients totally relapse free were less likely to develop accumulation of fixed disability (P <0.002). Multivariate analysis confirmed that a greater risk of accumulation of fixed disability was conferred by a higher Expanded Disability Status Scale (EDSS) score starting IFNbeta (P=0.02), and by failure of IFNbeta to completely suppress relapses (P=0.004). In conclusion, IFNbeta therapy reduced the accumulation of fixed disability in a cohort of RRMS patients, followed for a median of five years. Higher baseline EDSS and failure of complete relapse suppression were associated with a significantly greater likelihood of accumulation of fixed disability.

摘要

复发缓解型多发性硬化症(RRMS)患者中,拟议的β-干扰素(IFNβ)治疗失败标准尚未在临床实践中得到验证。本研究旨在确定:(a)与来自西尔维亚·劳里多发性硬化症研究中心的一组匹配的历史对照受试者相比,IFNβ是否减缓了固定残疾的累积;(b)基于复发的治疗失败标准或临床及人口统计学变量对固定残疾累积是否具有预测价值。在175例接受IFNβ治疗的RRMS患者中,60例(34%)在中位五年随访期内出现了固定残疾的累积,这显著低于对照组中固定残疾的累积率(P<0.0001)。治疗期间的任何一次复发预测固定残疾累积的敏感度为80%,特异度为43%;完全无复发的患者发生固定残疾累积的可能性较小(P<0.002)。多变量分析证实,开始使用IFNβ时较高的扩展残疾状态量表(EDSS)评分(P=0.02)以及IFNβ未能完全抑制复发(P=0.004)会带来更高的固定残疾累积风险。总之,在中位随访五年的RRMS患者队列中,IFNβ治疗减少了固定残疾的累积。较高的基线EDSS以及未能完全抑制复发与固定残疾累积的可能性显著增加相关。

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