Current and Emerging Treatment Options in Pediatric Onset Multiple Sclerosis

Sclerosis Pub Date : 2024-04-01 DOI:10.3390/sclerosis2020007
Artemis Mavridi, Maria-Eleni Bompou, Aine Redmond, Paraschos Archontakis-Barakakis, George D. Vavougios, D. Mitsikostas, T. Mavridis
{"title":"Current and Emerging Treatment Options in Pediatric Onset Multiple Sclerosis","authors":"Artemis Mavridi, Maria-Eleni Bompou, Aine Redmond, Paraschos Archontakis-Barakakis, George D. Vavougios, D. Mitsikostas, T. Mavridis","doi":"10.3390/sclerosis2020007","DOIUrl":null,"url":null,"abstract":"Pediatric onset multiple sclerosis (POMS), characterized by the onset of multiple sclerosis before the age of 18, is gaining increased recognition. Approximately 5 percent of MS cases manifest before the age of 18, with less than 1 percent occurring before the age of 10. Despite its rarity, pediatric MS exhibits distinct characteristics, with an association between younger age at onset and a comparatively slower disease progression. Despite this slower progression, individuals with POMS historically reach disability milestones at earlier ages than those with adult-onset multiple sclerosis. While various immunomodulatory agents demonstrate significant benefits in MS treatment, such as reduced relapse rates and slower accumulation of brain lesions on magnetic resonance imaging (MRI), the majority of disease-modifying therapies (DMTs) commonly used in adult MS lack evaluation through pediatric clinical trials. Current evidence is predominantly derived from observational studies. This comprehensive review aims to consolidate existing knowledge on the mechanisms of action, efficacy, safety profiles, and recommended dosages of available DMTs specifically in the context of pediatric MS. Furthermore, this review outlines recent advancements and explores potential medications still in developmental stages, providing a thorough overview of the current landscape and future prospects for treating POMS.","PeriodicalId":513065,"journal":{"name":"Sclerosis","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sclerosis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/sclerosis2020007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Pediatric onset multiple sclerosis (POMS), characterized by the onset of multiple sclerosis before the age of 18, is gaining increased recognition. Approximately 5 percent of MS cases manifest before the age of 18, with less than 1 percent occurring before the age of 10. Despite its rarity, pediatric MS exhibits distinct characteristics, with an association between younger age at onset and a comparatively slower disease progression. Despite this slower progression, individuals with POMS historically reach disability milestones at earlier ages than those with adult-onset multiple sclerosis. While various immunomodulatory agents demonstrate significant benefits in MS treatment, such as reduced relapse rates and slower accumulation of brain lesions on magnetic resonance imaging (MRI), the majority of disease-modifying therapies (DMTs) commonly used in adult MS lack evaluation through pediatric clinical trials. Current evidence is predominantly derived from observational studies. This comprehensive review aims to consolidate existing knowledge on the mechanisms of action, efficacy, safety profiles, and recommended dosages of available DMTs specifically in the context of pediatric MS. Furthermore, this review outlines recent advancements and explores potential medications still in developmental stages, providing a thorough overview of the current landscape and future prospects for treating POMS.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
小儿多发性硬化症的现有和新兴治疗方案
小儿多发性硬化症(POMS)的特点是在 18 岁之前发病,这种疾病正日益受到重视。约有 5% 的多发性硬化症患者在 18 岁前发病,不到 1% 的患者在 10 岁前发病。尽管少见,但小儿多发性硬化症表现出明显的特征,发病年龄较小,疾病进展相对较慢。尽管病程进展较慢,但与成人发病型多发性硬化症患者相比,小儿多发性硬化症患者达到残疾里程碑的年龄历来较早。虽然各种免疫调节药物在多发性硬化症的治疗中表现出显著的疗效,如降低复发率、减慢磁共振成像(MRI)上脑部病变的累积速度等,但大多数常用于成人多发性硬化症的疾病修饰疗法(DMTs)都没有通过儿科临床试验进行评估。目前的证据主要来自观察性研究。本综述旨在整合现有知识,特别是针对儿科多发性硬化症的现有 DMTs 的作用机制、疗效、安全性和推荐剂量。此外,本综述还概述了最新进展,并探讨了仍处于开发阶段的潜在药物,从而为治疗多发性硬化症的现状和未来前景提供了一个全面的概览。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Diet-Induced Changes in Functional Disability among People with Multiple Sclerosis: A Secondary Pooled Analysis of Two Randomized Controlled Pilot Trials Current and Emerging Treatment Options in Pediatric Onset Multiple Sclerosis Risk Factors for Cognitive Impairment in Multiple Sclerosis Patients Contextual Factors Matter: The Role of Social Support in Work-Related Difficulties and Employment Status in Persons with Multiple Sclerosis Role of Smartphone Applications in the Assessment and Management of Fatigue in Patients with Multiple Sclerosis: A Scoping Review
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1