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解读多发性硬化症的进展

Deciphering Multiple Sclerosis Progression.

作者信息

Meca-Lallana Virginia, Berenguer-Ruiz Leticia, Carreres-Polo Joan, Eichau-Madueño Sara, Ferrer-Lozano Jaime, Forero Lucía, Higueras Yolanda, Téllez Lara Nieves, Vidal-Jordana Angela, Pérez-Miralles Francisco Carlos

机构信息

Multiple Sclerosis Unit, Neurology Department, Fundación de Investigación Biomédica, Hospital Universitario de la Princesa, Madrid, Spain.

Neurology Department, Hospital Marina Baixa, Alicante, Spain.

出版信息

Front Neurol. 2021 Apr 7;12:608491. doi: 10.3389/fneur.2021.608491. eCollection 2021.

DOI:10.3389/fneur.2021.608491
PMID:33897583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8058428/
Abstract

Multiple sclerosis (MS) is primarily an inflammatory and degenerative disease of the central nervous system, triggered by unknown environmental factors in patients with predisposing genetic risk profiles. The prevention of neurological disability is one of the essential goals to be achieved in a patient with MS. However, the pathogenic mechanisms driving the progressive phase of the disease remain unknown. It was described that the pathophysiological mechanisms associated with disease progression are present from disease onset. In daily practice, there is a lack of clinical, radiological, or biological markers that favor an early detection of the disease's progression. Different definitions of disability progression were used in clinical trials. According to the most descriptive, progression was defined as a minimum increase in the Expanded Disability Status Scale (EDSS) of 1.5, 1.0, or 0.5 from a baseline level of 0, 1.0-5.0, and 5.5, respectively. Nevertheless, the EDSS is not the most sensitive scale to assess progression, and there is no consensus regarding any specific diagnostic criteria for disability progression. This review document discusses the current pathophysiological concepts associated with MS progression, the different measurement strategies, the biomarkers associated with disability progression, and the available pharmacologic therapeutic approaches.

摘要

多发性硬化症(MS)主要是一种中枢神经系统的炎症性和退行性疾病,由具有遗传易感性风险特征的患者中未知的环境因素引发。预防神经功能残疾是MS患者要实现的重要目标之一。然而,驱动疾病进展期的致病机制仍然未知。据描述,与疾病进展相关的病理生理机制在疾病发作时就已存在。在日常实践中,缺乏有助于早期检测疾病进展的临床、放射学或生物学标志物。临床试验中使用了不同的残疾进展定义。根据最具描述性的定义,进展分别定义为扩展残疾状态量表(EDSS)从基线水平0、1.0 - 5.0和5.5至少增加1.5、1.0或0.5。然而,EDSS并不是评估进展最敏感的量表,对于残疾进展的任何特定诊断标准也没有达成共识。本综述文件讨论了与MS进展相关的当前病理生理概念、不同的测量策略、与残疾进展相关的生物标志物以及可用的药物治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18ea/8058428/b2abcf8fd547/fneur-12-608491-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18ea/8058428/b2abcf8fd547/fneur-12-608491-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18ea/8058428/b2abcf8fd547/fneur-12-608491-g0001.jpg

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Multiple sclerosis and aging: comorbidity and treatment challenges.多发性硬化症与衰老:共病及治疗挑战
Mult Scler Relat Disord. 2021 May;50:102815. doi: 10.1016/j.msard.2021.102815. Epub 2021 Feb 4.
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Health care resource utilization and disease modifying treatment use in multiple sclerosis patients by age and insurance type.按年龄和保险类型划分的多发性硬化症患者的医疗资源利用和疾病修正治疗使用情况。
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Long-term follow-up from the ORATORIO trial of ocrelizumab for primary progressive multiple sclerosis: a post-hoc analysis from the ongoing open-label extension of the randomised, placebo-controlled, phase 3 trial.
中断疾病修正疗法对美国中年多发性硬化症患者医疗保健利用的影响。
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Psychological interventions for emotional well-being in adults with advanced progressive life-limiting illness.成人晚期进行性生命有限疾病的情绪幸福感的心理干预。
Cochrane Database Syst Rev. 2024 Oct 1;10(10):CD015421. doi: 10.1002/14651858.CD015421.
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Primary Progressive Multiple Sclerosis-A Key to Understanding and Managing Disease Progression.原发性进行性多发性硬化症——理解和管理疾病进展的关键。
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Protocol of a prospective multicenter study on comorbidity impact on multiple sclerosis and antibody-mediated diseases of the central nervous system (COMMIT).一项关于共病对多发性硬化症和中枢神经系统抗体介导疾病影响的前瞻性多中心研究方案(COMMIT)。
Front Immunol. 2024 Jul 2;15:1380025. doi: 10.3389/fimmu.2024.1380025. eCollection 2024.
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