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年龄对多发性硬化症疾病修正治疗转换或停药的影响。

Impact of Age on Switching or Stopping Disease Modifying Therapies in Multiple Sclerosis.

作者信息

Siddiqui Areeba, Hua Le H

机构信息

Southwest Medical Associates, Part of OptumCare, 4475 S Eastern Ave, Las Vegas, NV 89119, USA.

Cleveland Clinic Lou Ruvo Center for Brain Health, 888 W Bonneville Ave, Las Vegas, NV 89106, USA.

出版信息

Neurotherapeutics. 2025 Jul;22(4):e00603. doi: 10.1016/j.neurot.2025.e00603. Epub 2025 May 2.

DOI:10.1016/j.neurot.2025.e00603
PMID:40318957
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12418402/
Abstract

Older patients age ≥55 account for almost half of the total MS population. While focal inflammatory demyelinating processes and progressive processes such as compartmentalized CNS inflammation, neurodegeneration, and failure of compensatory mechanisms co-occur from disease onset, there is a shift in the predominant disease processes with notable clinical progression occurring in the fifth decade of life. Clinically, this manifests in reduction in clinical relapses and MRI activity as persons with MS age, with an increase in slow disability progression independent of relapses. As disease modifying therapies have demonstrated efficacy on relapse reduction, but not centrally mediated progressive processes, the benefit of DMT wanes with age due to change in underlying biological disease processes. Contrastingly, risks of DMTs increase due to biological changes related with age, setting up a scenario where considerations on switching or stopping DMT become more clinically important based on risk-benefit ratios. This review will cover evidence regarding DMT use in older patients with MS and discuss age considerations in the management of patients with MS.

摘要

年龄≥55岁的老年患者几乎占多发性硬化症(MS)总人口的一半。虽然从疾病发作开始就同时存在局灶性炎症性脱髓鞘过程和进行性过程,如局限性中枢神经系统炎症、神经退行性变和代偿机制衰竭,但随着年龄增长,主要疾病过程会发生转变,在生命的第五个十年会出现明显的临床进展。临床上,这表现为随着MS患者年龄增长,临床复发和MRI活动减少,与复发无关的缓慢残疾进展增加。由于疾病修饰疗法已证明对减少复发有效,但对中枢介导的进行性过程无效,由于潜在生物学疾病过程的变化,DMT的益处会随着年龄增长而减弱。相反,由于与年龄相关的生物学变化,DMT的风险增加,从而形成了一种情况,即基于风险效益比,关于更换或停用DMT的考虑在临床上变得更加重要。本综述将涵盖关于在老年MS患者中使用DMT的证据,并讨论MS患者管理中的年龄因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc45/12418402/0df27ef3b98c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc45/12418402/0df27ef3b98c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc45/12418402/0df27ef3b98c/gr1.jpg

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本文引用的文献

1
Discontinuation of First-Line Disease-Modifying Therapy in Patients With Stable Multiple Sclerosis: The DOT-MS Randomized Clinical Trial.稳定型多发性硬化症患者一线疾病修正治疗的停药:DOT-MS随机临床试验
JAMA Neurol. 2025 Feb 1;82(2):123-131. doi: 10.1001/jamaneurol.2024.4164.
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De-escalation from anti-CD20 to cladribine tablets in multiple sclerosis: A pilot study.多发性硬化症中从抗CD20治疗降级为使用克拉屈滨片的初步研究。
Mult Scler Relat Disord. 2024 Dec;92:106145. doi: 10.1016/j.msard.2024.106145. Epub 2024 Oct 28.
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Differential Diagnosis of Suspected Multiple Sclerosis in Pediatric and Late-Onset Populations: A Review.
儿童及晚发性人群疑似多发性硬化症的鉴别诊断:综述
JAMA Neurol. 2024 Sep 16. doi: 10.1001/jamaneurol.2024.3062.
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Effect of Prior Treatment With Fingolimod on Early and Late Response to Rituximab/Ocrelizumab in Patients With Multiple Sclerosis.先前使用芬戈莫德对多发性硬化症患者接受利妥昔单抗/奥瑞珠单抗的早期和晚期反应的影响。
Neurol Neuroimmunol Neuroinflamm. 2024 May;11(3):e200231. doi: 10.1212/NXI.0000000000200231. Epub 2024 Apr 16.
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High-Efficacy Therapy Discontinuation vs Continuation in Patients 50 Years and Older With Nonactive MS.50 岁及以上非活动期多发性硬化症患者的高效疗法停药与继续治疗。
JAMA Neurol. 2024 May 1;81(5):490-498. doi: 10.1001/jamaneurol.2024.0395.
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Clinical and Treatment Considerations for the Pediatric and Aging Patients with Multiple Sclerosis.多发性硬化症儿科和老年患者的临床和治疗注意事项。
Neurol Clin. 2024 Feb;42(1):255-274. doi: 10.1016/j.ncl.2023.07.003. Epub 2023 Aug 23.
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Immunosenescence and multiple sclerosis: inflammaging for prognosis and therapeutic consideration.免疫衰老与多发性硬化症:炎症衰老对预后及治疗的考量
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Stopping Disease-Modifying Treatments in Multiple Sclerosis: A Systematic Review and Meta-Analysis of Real-World Studies.停止多发性硬化症的疾病修饰治疗:一项对真实世界研究的系统评价和荟萃分析
CNS Drugs. 2023 Oct;37(10):915-927. doi: 10.1007/s40263-023-01038-z. Epub 2023 Sep 23.
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