Relapse-Associated and Relapse-Independent Contribution to Overall Expanded Disability Status Scale Progression in Multiple Sclerosis Patients Diagnosed in Different Eras.

IF 8.1 1区 医学 Q1 CLINICAL NEUROLOGY
Noemi Montobbio, Cinzia Cordioli, Alessio Signori, Francesca Bovis, Ruggero Capra, Maria Pia Sormani
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Abstract

Objective: The introduction of disease-modifying therapies for multiple sclerosis (MS) has led to a deceleration of disease course over the years. Although decreased relapse rate constitutes a factor, the role of relapse-associated worsening (RAW) and progression independent of relapse activity (PIRA) in MS course deceleration is still unclear.

Methods: We retrospectively examined long-term Expanded Disability Status Scale (EDSS) progression in patients referred to the MS Center of Montichiari (Italy) and diagnosed with relapsing-remitting MS from 1980 to 2022. To isolate PIRA, we deducted all EDSS changes associated with relapses from overall EDSS change. We compared the relative contribution of PIRA and RAW to EDSS progression in patients diagnosed in different periods using mixed-effects models.

Results: A total of 1,405 patients were included in the study, of whom 231 were diagnosed in 1980-1996 (pre-treatment era), 577 in 1997-2008 (injectable disease-modifying therapy era), and 597 after 2008 (oral drugs, monoclonal antibodies, and anti-CD20 era). Across ages, both PIRA and RAW were reduced in patients diagnosed in more recent periods as compared with earlier periods. The average contribution of PIRA to overall EDSS progression was already predominant in patients diagnosed in 1980-1996 (78%) and in 1997-2008 (76%), but it was significantly increased (p = 0.0009) in patients diagnosed in later years (87%).

Interpretation: The deceleration of MS course observed throughout the years is determined not only by fewer RAW events, but also by a reduction in PIRA. However, the shift toward a mostly relapse-independent progression highlights the importance of evaluating new therapies based on their effect on PIRA. ANN NEUROL 2024.

不同时期确诊的多发性硬化症患者的复发相关性和复发依赖性对总体残疾状况扩展量表进展的影响
目的:多年来,针对多发性硬化症(MS)的疾病改变疗法的引入导致了病程的减缓。虽然复发率下降是一个因素,但复发相关恶化(RAW)和独立于复发活动的进展(PIRA)在多发性硬化病程减速中的作用仍不清楚:我们回顾性研究了1980年至2022年期间转诊至意大利蒙蒂奇亚里多发性硬化症中心并被诊断为复发缓解型多发性硬化症患者的长期扩展残疾状态量表(EDSS)进展情况。为了分离出 PIRA,我们从 EDSS 整体变化中扣除了所有与复发相关的 EDSS 变化。我们使用混合效应模型比较了PIRA和RAW对不同时期确诊患者EDSS进展的相对贡献:研究共纳入了 1,405 例患者,其中 231 例确诊于 1980-1996 年(前治疗时代),577 例确诊于 1997-2008 年(可注射的疾病修饰疗法时代),597 例确诊于 2008 年之后(口服药物、单克隆抗体和抗 CD20 时代)。从各年龄段来看,近期诊断的患者的 PIRA 和 RAW 均低于早期诊断的患者。在1980-1996年(78%)和1997-2008年(76%)确诊的患者中,PIRA对总体EDSS进展的平均贡献率已占主导地位,但在晚期确诊的患者(87%)中,PIRA的贡献率显著增加(p = 0.0009):多年来观察到的多发性硬化症病程减慢不仅取决于 RAW 事件的减少,还取决于 PIRA 的减少。然而,向大部分不依赖复发进展的转变凸显了根据对 PIRA 的影响评估新疗法的重要性。ann neurol 2024.
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来源期刊
Annals of Neurology
Annals of Neurology 医学-临床神经学
CiteScore
18.00
自引率
1.80%
发文量
270
审稿时长
3-8 weeks
期刊介绍: Annals of Neurology publishes original articles with potential for high impact in understanding the pathogenesis, clinical and laboratory features, diagnosis, treatment, outcomes and science underlying diseases of the human nervous system. Articles should ideally be of broad interest to the academic neurological community rather than solely to subspecialists in a particular field. Studies involving experimental model system, including those in cell and organ cultures and animals, of direct translational relevance to the understanding of neurological disease are also encouraged.
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