多发性硬化症复发的皮质类固醇治疗与5年内较低的残疾恶化有关。

IF 7.5 1区 医学 Q1 CLINICAL NEUROLOGY
Jodie I Roberts, Sifat Sharmin, Dana Horakova, Eva Kubala Havrdova, Serkan Ozakbas, Alessandra Lugaresi, Valentina Tomassini, Raed Alroughani, Katherine Buzzard, Olga Skibina, Cavit Boz, Recai Turkoglu, Davide Maimone, Bassem Yamout, Samia Joseph Khoury, Daniele Spitaleri, Jeannette Lechner-Scott, Marc Girard, Pierre Duquette, Abdullah Al-Asmi, Radek Ampapa, Matteo Foschi, Andrea Surcinelli, Francesco Patti, Vincent Van Pesch, Cristina Ramo-Tello, José Luis Sánchez-Menoyo, Ayse Altintas, Pierre Grammond, Elisabetta Cartechini, Tunde Csepany, Guy Laureys, Barbara Willekens, Izanne Roos, Tomas Kalincik, MSBase Study Group
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引用次数: 0

摘要

背景:皮质类固醇治疗多发性硬化症(MS)复发被认为可以提高复发恢复的速度,而不会改变长期残疾的风险。我们的目的是在MS患者的大队列中重新评估这一假设。方法:在国际神经免疫学登记MSBase中确定临床明确的MS患者和≥3个扩展残疾状态量表(EDSS)测量≥12个月的个体。个体必须有≥1次复发,并具有所有记录的复发治疗、表型和严重程度的完整信息。主要结果为12个月以上确认的残疾恶化。使用Cox比例风险评估类固醇治疗和未治疗的累计复发次数(作为时变暴露)与残疾恶化的关系。结果:共有3673人符合纳入标准(71%为女性,平均年龄38岁,平均残疾EDSS第2步);5809例复发(治疗4671例/未治疗1138例)(年复发率0.19)。在研究期间(共30175人年),32.7%的患者达到了确认残疾恶化的结果(中位生存时间5.2年)。未治疗的复发与类固醇治疗的复发(HR 1.50, 95% CI 1.43 - 1.57)相比,残疾恶化的风险更高(HR 1.72, 95% CI 1.57 - 1.88)。这种关联被复发时疾病改善治疗的疗效所改变。结论:我们的研究结果表明,MS复发缺乏类固醇治疗与未来残疾恶化的高风险相关。因此,皮质类固醇治疗多发性硬化症复发不仅会影响恢复速度,还会影响残余结构损伤的严重程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Corticosteroid treatment of multiple sclerosis relapses is associated with lower disability worsening over 5 years.

Background: Corticosteroid treatment of multiple sclerosis (MS) relapses is assumed to improve the speed of relapse recovery, without modifying long-term disability risk. We aimed to re-evaluate this assumption in a large cohort of individuals with MS.

Methods: Individuals with clinically definite MS and ≥3 Expanded Disability Status Scale (EDSS) measurements over ≥12 months were identified within the international neuroimmunology registry MSBase. Individuals were required to have ≥1 relapse, with complete information on relapse treatment, phenotype and severity for all documented relapses. The primary outcome was disability worsening confirmed over 12 months. The association of the cumulative number of steroid-treated and untreated relapses (as a time-varying exposure) with disability worsening was evaluated with Cox proportional hazards.

Results: In total, 3673 individuals met the inclusion criteria (71% female, mean age 38 years, mean disability EDSS step 2); 5809 relapses (4671 treated/1138 untreated) were captured (annualised relapse rate 0.19). Over the study period (total 30 175 person-years), 32.7% reached the outcome of confirmed disability worsening (median survival time 5.2 years). Non-treated relapses were associated with a higher risk of disability worsening (HR 1.72, 95% CI 1.57 to 1.88) than steroid-treated relapses (HR 1.50, 95% CI 1.43 to 1.57). This association was modified by the efficacy of disease-modifying therapy at the time of relapse.

Conclusions: Our results suggest that a lack of steroid treatment of MS relapses is associated with a higher risk of future disability worsening. Hence, corticosteroid treatment of MS relapses may impact not only the speed of recovery but also the severity of residual structural damage.

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来源期刊
CiteScore
15.70
自引率
1.80%
发文量
888
审稿时长
6 months
期刊介绍: The Journal of Neurology, Neurosurgery & Psychiatry (JNNP) aspires to publish groundbreaking and cutting-edge research worldwide. Covering the entire spectrum of neurological sciences, the journal focuses on common disorders like stroke, multiple sclerosis, Parkinson’s disease, epilepsy, peripheral neuropathy, subarachnoid haemorrhage, and neuropsychiatry, while also addressing complex challenges such as ALS. With early online publication, regular podcasts, and an extensive archive collection boasting the longest half-life in clinical neuroscience journals, JNNP aims to be a trailblazer in the field.
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