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多发性硬化症的自然病史:基于地理的研究 10:复发和长期残疾。

The natural history of multiple sclerosis: a geographically based study 10: relapses and long-term disability.

机构信息

Imperial College, Division of Neuroscience, London, UK.

出版信息

Brain. 2010 Jul;133(Pt 7):1914-29. doi: 10.1093/brain/awq118. Epub 2010 Jun 9.

DOI:10.1093/brain/awq118
PMID:20534650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2892939/
Abstract

The relationship of relapses to long-term disability in multiple sclerosis is uncertain. Relapse reduction is a common therapeutic target but clinical trials have shown dissociation between relapse suppression and disability accumulation. We investigated relationships between relapses and disability progression for outcomes of requiring assistance to walk, being bedridden and dying from multiple sclerosis [Disability Status Scale 6, 8, 10] by analysing 28 000 patient-years of evolution in 806-bout onset patients from the London Ontario natural history cohort. Having previously shown no effect of relapse frequency among progressive multiple sclerosis subtypes, here we examined these measures in the pre-progressive or relapsing-remitting phase. Survival was compared among groups stratified by (i) early relapses--number of attacks during the first 2 years of multiple sclerosis; (ii) length of first inter-attack interval; (iii) interval between onset and Disability Status Scale 3 (moderate disability); (iv) number of attacks from the third year of disease up to onset of progression; and (v) during the entire relapsing-remitting phase. Early clinical features can predict hard disability outcomes. Frequent relapses in the first 2 years and shorter first inter-attack intervals predicted shorter times to reach hard disability endpoints. Attack frequencies, in the first 2 years, of 1 versus >or=3, gave differences of 7.6, 12.8 and 20.3 years in times from disease onset to Disability Status Scale 6, 8 and 10, respectively. Time to Disability Status Scale 3 highly and independently predicted time to Disability Status Scale 6, 8 and 10. In contrast, neither total number of relapsing-remitting phase attacks nor of relapses experienced during the relapsing-remitting phase after the second year up to onset of progression showed a deleterious effect on times from disease onset, from progression onset and from Disability Status Scale 3 to these hard endpoints. The failure of a regulatory mechanism tied to neurodegeneration is suggested. Relapse frequency beyond Year 2 does not appear to predict the key outcome of secondary progression or times to Disability Status Scale 6, 8 or 10, highlighting two distinct disease phases related to late outcome. These appear to be separated by a watershed within the relapsing-remitting phase, just a few years after clinical onset. Higher early relapse frequencies and shorter first inter-attack intervals herald more rapid deterioration via interaction with the neurodegeneration characterizing secondary progression. They increase the probability of its occurrence, its latency and influence--to a lesser degree--its slope. The prevention or delay of the progressive phase of the disease is implicated as a key therapeutic target in relapsing-remitting patients.

摘要

多发性硬化症患者复发与长期残疾之间的关系尚不确定。减少复发是常见的治疗目标,但临床试验表明复发抑制与残疾累积之间存在差异。我们通过分析来自伦敦安大略自然史队列的 806 例首发患者 28000 患者年的演变,研究了需要辅助行走、卧床不起和死于多发性硬化症的残疾进展结局[残疾状况量表 6、8、10]与复发之间的关系。我们之前在进行性多发性硬化症亚型中没有发现复发频率的影响,因此在此我们在进展前或复发缓解期检查了这些指标。根据以下因素对各组进行分层,比较了生存情况:(i)早期复发-多发性硬化症前 2 年的发作次数;(ii)首次发作间隔时间;(iii)发病至残疾状况量表 3(中度残疾)的间隔时间;(iv)从疾病第 3 年到进展开始的发作次数;以及(v)整个复发缓解期。早期临床特征可预测严重残疾结局。前 2 年频繁发作和较短的首次发作间隔预示着更快达到严重残疾终点。在疾病发作后前 2 年的发作频率为 1 次与≥3 次,分别在从疾病发作到残疾状况量表 6、8 和 10 的时间上有 7.6、12.8 和 20.3 年的差异。残疾状况量表 3 的时间高度独立地预测了残疾状况量表 6、8 和 10 的时间。相比之下,复发缓解期发作的总数或复发缓解期发作的次数,在第 2 年以后到进展开始之间,对从疾病发作、从进展开始到残疾状况量表 3 到这些严重终点的时间均没有不利影响。提示存在与神经退行性变相关的调节机制失败。复发频率超过第 2 年似乎并不预示着二级进展或残疾状况量表 6、8 或 10 的关键结局,突出了与晚期结局相关的两个不同疾病阶段。这些阶段似乎在疾病发作后几年内通过与二级进展特征性的神经退行性变相互作用,在复发缓解期内分离。较高的早期复发频率和较短的首次发作间隔预示着通过与二级进展特征性的神经退行性变相互作用,更快的恶化。它们增加了疾病进展发生的概率、潜伏期和影响(程度较小),但影响其斜率。因此,在复发缓解型患者中,预防或延迟疾病的进展阶段可能成为一个关键的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e939/2892939/c94b3a9e97f9/awq118f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e939/2892939/115e1852518f/awq118f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e939/2892939/e75de4b4c832/awq118f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e939/2892939/c94b3a9e97f9/awq118f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e939/2892939/115e1852518f/awq118f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e939/2892939/e75de4b4c832/awq118f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e939/2892939/c94b3a9e97f9/awq118f3.jpg

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