María Agustina Zárate , Mariano Marrodan , María Agustina Piedrabuena , Marcela Paula Fiol , María Célica Ysrraelit , Jorge Correale
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Patients were categorized as EP (PIRA within five years of onset) or late PIRA (LP, after five years). Cox regression and Kaplan-Meier survival analyses assessed risk factors and disability progression.</div></div><div><h3>Results</h3><div>EP was identified in 39/77 (51 %) of PIRA patients. EP patients were older at diagnosis (38.6 vs. 34 years, <em>p</em> = 0.01), predominantly female (<em>p</em> = 0.02), and more likely to have spinal cord onset symptoms (<em>p</em> < 0.01). EP patients reached EDSS 4, 6, and 8 significantly faster than LP patients (<em>p</em> < 0.01). In multivariate analysis, spinal cord onset was the strongest predictor of EP (HR=2.1, 95 %CI=1.05–4.44, <em>p</em> = 0.03).</div></div><div><h3>Conclusions</h3><div>EP occurs in half of PIRA patients and is associated with spinal cord onset and older age at diagnosis. These findings highlight the need for early identification and aggressive treatment to mitigate long-term disability. Further research is required to refine predictive models and optimize therapeutic strategies for high-risk patients.</div></div>","PeriodicalId":18958,"journal":{"name":"Multiple sclerosis and related disorders","volume":"100 ","pages":"Article 106529"},"PeriodicalIF":2.9000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Development of early progression independent of relapse activity significantly impacts on disability accumulation in patients with multiple sclerosis\",\"authors\":\"María Agustina Zárate , Mariano Marrodan , María Agustina Piedrabuena , Marcela Paula Fiol , María Célica Ysrraelit , Jorge Correale\",\"doi\":\"10.1016/j.msard.2025.106529\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Disability accumulation in multiple sclerosis (MS) is driven by relapse-associated worsening (RAW) and progression independent of relapse activity (PIRA). Early PIRA (EP), occurring within five years of disease onset, has been proposed as a critical marker of poor prognosis. However, risk factors for EP remain poorly defined.</div></div><div><h3>Objective</h3><div>To identify clinical and demographic factors associated with EP and assess its impact on long-term disability accumulation.</div></div><div><h3>Methods</h3><div>This retrospective cohort study included 143 relapsing-remitting MS patients with disability progression (EDSS 4, 6, or 8) primarily due to PIRA. Patients were categorized as EP (PIRA within five years of onset) or late PIRA (LP, after five years). Cox regression and Kaplan-Meier survival analyses assessed risk factors and disability progression.</div></div><div><h3>Results</h3><div>EP was identified in 39/77 (51 %) of PIRA patients. EP patients were older at diagnosis (38.6 vs. 34 years, <em>p</em> = 0.01), predominantly female (<em>p</em> = 0.02), and more likely to have spinal cord onset symptoms (<em>p</em> < 0.01). EP patients reached EDSS 4, 6, and 8 significantly faster than LP patients (<em>p</em> < 0.01). In multivariate analysis, spinal cord onset was the strongest predictor of EP (HR=2.1, 95 %CI=1.05–4.44, <em>p</em> = 0.03).</div></div><div><h3>Conclusions</h3><div>EP occurs in half of PIRA patients and is associated with spinal cord onset and older age at diagnosis. These findings highlight the need for early identification and aggressive treatment to mitigate long-term disability. Further research is required to refine predictive models and optimize therapeutic strategies for high-risk patients.</div></div>\",\"PeriodicalId\":18958,\"journal\":{\"name\":\"Multiple sclerosis and related disorders\",\"volume\":\"100 \",\"pages\":\"Article 106529\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-05-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Multiple sclerosis and related disorders\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2211034825002718\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Multiple sclerosis and related disorders","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211034825002718","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景:多发性硬化症(MS)的残疾积累是由复发相关恶化(RAW)和独立于复发活动(PIRA)的进展驱动的。早期PIRA (EP),发生在疾病发病的五年内,被认为是预后不良的关键标志。然而,EP的危险因素仍然不明确。目的探讨EP相关的临床和人口学因素,并评估其对长期残疾积累的影响。方法:本回顾性队列研究纳入143例主要因PIRA导致残疾进展(EDSS 4、6或8)的复发缓解型MS患者。患者分为EP(发病5年内发生PIRA)和晚发性PIRA(发病5年后发生LP)。Cox回归和Kaplan-Meier生存分析评估了危险因素和残疾进展。结果PIRA患者中有39/77(51%)存在sep。EP患者在诊断时年龄较大(38.6 vs. 34岁,p = 0.01),以女性为主(p = 0.02),且更有可能出现脊髓发病症状(p <;0.01)。EP患者达到EDSS 4、6、8的时间明显快于LP患者(p <;0.01)。在多变量分析中,脊髓发病是EP的最强预测因子(HR=2.1, 95% CI= 1.05-4.44, p = 0.03)。结论半数PIRA患者出现sep,与脊髓发病和诊断年龄较大有关。这些发现强调了早期识别和积极治疗以减轻长期残疾的必要性。需要进一步的研究来完善预测模型和优化高危患者的治疗策略。
Development of early progression independent of relapse activity significantly impacts on disability accumulation in patients with multiple sclerosis
Background
Disability accumulation in multiple sclerosis (MS) is driven by relapse-associated worsening (RAW) and progression independent of relapse activity (PIRA). Early PIRA (EP), occurring within five years of disease onset, has been proposed as a critical marker of poor prognosis. However, risk factors for EP remain poorly defined.
Objective
To identify clinical and demographic factors associated with EP and assess its impact on long-term disability accumulation.
Methods
This retrospective cohort study included 143 relapsing-remitting MS patients with disability progression (EDSS 4, 6, or 8) primarily due to PIRA. Patients were categorized as EP (PIRA within five years of onset) or late PIRA (LP, after five years). Cox regression and Kaplan-Meier survival analyses assessed risk factors and disability progression.
Results
EP was identified in 39/77 (51 %) of PIRA patients. EP patients were older at diagnosis (38.6 vs. 34 years, p = 0.01), predominantly female (p = 0.02), and more likely to have spinal cord onset symptoms (p < 0.01). EP patients reached EDSS 4, 6, and 8 significantly faster than LP patients (p < 0.01). In multivariate analysis, spinal cord onset was the strongest predictor of EP (HR=2.1, 95 %CI=1.05–4.44, p = 0.03).
Conclusions
EP occurs in half of PIRA patients and is associated with spinal cord onset and older age at diagnosis. These findings highlight the need for early identification and aggressive treatment to mitigate long-term disability. Further research is required to refine predictive models and optimize therapeutic strategies for high-risk patients.
期刊介绍:
Multiple Sclerosis is an area of ever expanding research and escalating publications. Multiple Sclerosis and Related Disorders is a wide ranging international journal supported by key researchers from all neuroscience domains that focus on MS and associated disease of the central nervous system. The primary aim of this new journal is the rapid publication of high quality original research in the field. Important secondary aims will be timely updates and editorials on important scientific and clinical care advances, controversies in the field, and invited opinion articles from current thought leaders on topical issues. One section of the journal will focus on teaching, written to enhance the practice of community and academic neurologists involved in the care of MS patients. Summaries of key articles written for a lay audience will be provided as an on-line resource.
A team of four chief editors is supported by leading section editors who will commission and appraise original and review articles concerning: clinical neurology, neuroimaging, neuropathology, neuroepidemiology, therapeutics, genetics / transcriptomics, experimental models, neuroimmunology, biomarkers, neuropsychology, neurorehabilitation, measurement scales, teaching, neuroethics and lay communication.