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多发性硬化症的十年预后:复发缓解型患者预后较好,但原发进展型患者并非如此。

Ten-year prognosis in multiple sclerosis: a better outcome in relapsing-remitting patients but not in primary progressive patients.

作者信息

Kerbrat A, Hamonic S, Leray E, Tron I, Edan G, Yaouanq J

机构信息

Department of Neurology, University Hospital, Rennes, France; WENNE, Grand-Ouest, France.

出版信息

Eur J Neurol. 2015 Mar;22(3):507-e35. doi: 10.1111/ene.12600. Epub 2014 Dec 16.

Abstract

BACKGROUND AND PURPOSE

Multiple sclerosis (MS) prognosis remains a challenge for both patients and physicians. Complementary to natural history studies, updated population-based data from the first event suggestive of MS, at the time of the first approved disease modifying drug (DMD), are needed. Our objective was to provide a 10-year history of MS from clinical onset at time of first approved DMDs in a population-based cohort.

METHODS

A population-based cohort of patients whose first clinical event suggestive of MS had occurred in Brittany between 2000 and 2001 was prospectively selected. History of relapses, treatments and disability up to 10 years after onset were collected.

RESULTS

In all, 278 patients with either attack-onset (n = 244) or progressive-onset (n = 34) were recruited. Amongst attack-onset patients, 30% remained as clinically isolated syndrome and 70% had a second relapse after a median time of 1.7 years (95% confidence interval 1.2-2.4). 80% of relapsing-remitting MS patients received DMDs for at least 6 months. 29% reached disability status scale (DSS) 3 and 8% DSS 6. Amongst progressive-onset patients, 100% reached DSS 3 and 59% DSS 6.

CONCLUSION(S): Our population-based study reports a lower risk of disability progression at 10-year follow-up in the relapsing-remitting MS group than previously reported. This better prognosis was not observed in the progressive-onset MS group. This finding impacts the prognosis given to patients in clinical practice.

摘要

背景与目的

对患者和医生而言,多发性硬化症(MS)的预后仍然是一项挑战。作为对自然史研究的补充,需要从首次出现提示MS的事件起,到首次批准使用疾病修正药物(DMD)时基于人群的最新数据。我们的目标是在一个基于人群的队列中,提供从首次批准使用DMD时起10年的MS临床发病病史。

方法

前瞻性选取了一个基于人群的队列,这些患者在2000年至2001年期间于布列塔尼首次出现提示MS的临床事件。收集了发病后长达10年的复发、治疗和残疾史。

结果

共招募了278例发作性起病(n = 244)或进展性起病(n = 34)的患者。在发作性起病的患者中,30%仍为临床孤立综合征,70%在中位时间1.7年(95%置信区间1.2 - 2.4)后出现第二次复发。80%的复发缓解型MS患者接受DMD治疗至少6个月。29%达到残疾状态量表(DSS)3级,8%达到DSS 6级。在进展性起病的患者中,100%达到DSS 3级,59%达到DSS 6级。

结论

我们基于人群的研究报告显示,复发缓解型MS组在10年随访时残疾进展风险低于先前报道。进展性起病的MS组未观察到这种较好的预后。这一发现影响了临床实践中给予患者的预后判断。

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