• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

临床视角:如何实现多发性硬化症的个性化治疗,以及包括影像学在内的生物标志物对此能有何帮助?

The clinical perspective: How to personalise treatment in MS and how may biomarkers including imaging contribute to this?

作者信息

Vermersch Patrick, Berger Thomas, Gold Ralf, Lukas Carsten, Rovira Alex, Meesen Bianca, Chard Declan, Comabella Manuel, Palace Jacqueline, Trojano Maria

机构信息

University of Lille, CHRU de Lille, Lille International Research Inflammation Center (LIRIC), INSRRM U995, FHU Imminent, Lille, France

Neuroimmunology and Multiple Sclerosis Clinic, Medical University of Innsbruck (MUI), Innsbruck, Austria.

出版信息

Mult Scler. 2016 Aug;22(2 Suppl):18-33. doi: 10.1177/1352458516650739.

DOI:10.1177/1352458516650739
PMID:27465613
Abstract

BACKGROUND

Multiple sclerosis (MS) is a highly heterogeneous disease, both in its course and in its response to treatments. Effective biomarkers may help predict disability progression and monitor patients' treatment responses.

OBJECTIVE

The aim of this review was to focus on how biomarkers may contribute to treatment individualisation in MS patients.

METHODS

This review reflects the content of presentations, polling results and discussions on the clinical perspective of MS during the first and second Pan-European MS Multi-stakeholder Colloquia in Brussels in May 2014 and 2015.

RESULTS

In clinical practice, magnetic resonance imaging (MRI) measures play a significant role in the diagnosis and follow-up of MS patients. Together with clinical markers, the rate of MRI-visible lesion accrual once a patient has started treatment may also help to predict subsequent treatment responsiveness. In addition, several molecular (immunological, genetic) biomarkers have been established that may play a role in predictive models of MS relapses and progression. To reach personalised treatment decisions, estimates of disability progression and likely treatment response should be carefully considered alongside the risk of serious adverse events, together with the patient's treatment expectations.

CONCLUSION

Although biomarkers may be very useful for individualised decision making in MS, many are still research tools and need to be validated before implementation in clinical practice.

摘要

背景

多发性硬化症(MS)在病程和对治疗的反应方面都是一种高度异质性疾病。有效的生物标志物可能有助于预测残疾进展并监测患者的治疗反应。

目的

本综述的目的是聚焦于生物标志物如何有助于MS患者的个体化治疗。

方法

本综述反映了2014年5月和2015年5月在布鲁塞尔举行的第一届和第二届泛欧洲MS多利益相关方研讨会上关于MS临床视角的报告内容、投票结果和讨论。

结果

在临床实践中,磁共振成像(MRI)测量在MS患者的诊断和随访中发挥着重要作用。与临床标志物一起,患者开始治疗后MRI可见病灶累积率也可能有助于预测后续治疗反应性。此外,已经确定了几种分子(免疫、遗传)生物标志物,它们可能在MS复发和进展的预测模型中发挥作用。为了做出个性化的治疗决策,在考虑严重不良事件风险以及患者的治疗期望的同时,应仔细考虑残疾进展估计和可能的治疗反应。

结论

尽管生物标志物可能对MS的个体化决策非常有用,但许多仍然是研究工具,在临床实践中实施之前需要进行验证。

相似文献

1
The clinical perspective: How to personalise treatment in MS and how may biomarkers including imaging contribute to this?临床视角:如何实现多发性硬化症的个性化治疗,以及包括影像学在内的生物标志物对此能有何帮助?
Mult Scler. 2016 Aug;22(2 Suppl):18-33. doi: 10.1177/1352458516650739.
2
Conclusions: Calls to action for improving the life of MS patients and their families.结论:呼吁采取行动改善多发性硬化症患者及其家庭的生活。
Mult Scler. 2016 Aug;22(2 Suppl):71-7. doi: 10.1177/1352458516650738.
3
The importance of a multi-disciplinary perspective and patient activation programmes in MS management.多学科视角和患者激活计划在多发性硬化症管理中的重要性。
Mult Scler. 2016 Aug;22(2 Suppl):34-46. doi: 10.1177/1352458516650741.
4
Introduction: Do we need multi-stakeholder colloquia in MS?引言:在多发性硬化症中我们是否需要多方利益相关者座谈会?
Mult Scler. 2016 Aug;22(2 Suppl):4-8. doi: 10.1177/1352458516650740.
5
The payer's perspective: What is the burden of MS and how should the patient's perspective be integrated in health technology assessment conducted for taking decisions on access to care and treatment?支付方的观点:多发性硬化症的负担是什么,以及在进行卫生技术评估以决定获得护理和治疗的机会时,应如何将患者的观点纳入其中?
Mult Scler. 2016 Aug;22(2 Suppl):60-70. doi: 10.1177/1352458516650743.
6
The patient's perspective: How to create awareness for improving access to care and treatment of MS patients?患者视角:如何提高对改善多发性硬化症患者获得护理和治疗机会的认识?
Mult Scler. 2016 Aug;22(2 Suppl):9-17. doi: 10.1177/1352458516650742.
7
The regulator's perspective: How should new therapies and follow-on products for MS be clinically evaluated in the future?监管机构的观点:未来多发性硬化症的新疗法和后续产品应如何进行临床评估?
Mult Scler. 2016 Aug;22(2 Suppl):47-59. doi: 10.1177/1352458516650744.
8
Preface.前言。
Mult Scler. 2016 Aug;22(2 Suppl):2-3. doi: 10.1177/1352458516650745.
9
Precision medicine in multiple sclerosis: biomarkers for diagnosis, prognosis, and treatment response.多发性硬化症的精准医学:用于诊断、预后及治疗反应的生物标志物
Curr Opin Neurol. 2016 Jun;29(3):254-62. doi: 10.1097/WCO.0000000000000336.
10
A Bayesian hierarchical surrogate outcome model for multiple sclerosis.一种用于多发性硬化症的贝叶斯分层替代结局模型。
Pharm Stat. 2016 Jul;15(4):341-8. doi: 10.1002/pst.1749. Epub 2016 Apr 7.

引用本文的文献

1
The Role of Advanced Magnetic Resonance Imaging Sequences in Multiple Sclerosis.先进磁共振成像序列在多发性硬化症中的作用
Cureus. 2024 Aug 25;16(8):e67759. doi: 10.7759/cureus.67759. eCollection 2024 Aug.
2
Soluble CD40 Ligand as a Promising Biomarker in Cancer Diagnosis.可溶性 CD40 配体作为癌症诊断中有前途的生物标志物。
Cells. 2024 Jul 28;13(15):1267. doi: 10.3390/cells13151267.
3
New Enhancing MRI Lesions Associate with IL-17, Neutrophil Degranulation and Integrin Microparticles: Multi-Omics Combined with Frequent MRI in Multiple Sclerosis.
新的增强型磁共振成像病变与白细胞介素-17、中性粒细胞脱颗粒和整合素微粒相关:多组学结合多发性硬化症的频繁磁共振成像
Biomedicines. 2023 Nov 28;11(12):3170. doi: 10.3390/biomedicines11123170.
4
A Scoping Review on Body Fluid Biomarkers for Prognosis and Disease Activity in Patients with Multiple Sclerosis.多发性硬化症患者预后和疾病活动的体液生物标志物的范围综述
J Pers Med. 2022 Aug 31;12(9):1430. doi: 10.3390/jpm12091430.
5
Effects of Lactobacillus casei Strain T2 (IBRC-M10783) on the Modulation of Th17/Treg and Evaluation of miR-155, miR-25, and IDO-1 Expression in a Cuprizone-Induced C57BL/6 Mouse Model of Demyelination.干酪乳杆菌 T2(IBRC-M10783)对髓鞘脱失 C57BL/6 小鼠模型中 Th17/Treg 调节及 miR-155、miR-25、IDO-1 表达的影响。
Inflammation. 2021 Feb;44(1):334-343. doi: 10.1007/s10753-020-01339-1. Epub 2020 Sep 10.
6
Molecular biomarkers in multiple sclerosis.多发性硬化症的分子生物标志物。
J Neuroinflammation. 2019 Dec 23;16(1):272. doi: 10.1186/s12974-019-1674-2.
7
Anti-Myelin Oligodendrocyte Glycoprotein and Human Leukocyte Antigens as Markers in Pediatric and Adolescent Multiple Sclerosis: on Diagnosis, Clinical Phenotypes, and Therapeutic Responses.抗髓鞘少突胶质细胞糖蛋白和人类白细胞抗原作为儿童及青少年多发性硬化症的标志物:关于诊断、临床表型及治疗反应
Mult Scler Int. 2018 Nov 22;2018:8487471. doi: 10.1155/2018/8487471. eCollection 2018.
8
Perspectives of Patients with Multiple Sclerosis on Drug Treatment: A Qualitative Study.多发性硬化症患者对药物治疗的看法:一项定性研究。
Int J MS Care. 2018 Nov-Dec;20(6):269-277. doi: 10.7224/1537-2073.2017-109.
9
Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis.研究 microRNA 和转录因子共调控网络在多发性硬化症发病机制中的作用。
Int J Mol Sci. 2018 Nov 20;19(11):3652. doi: 10.3390/ijms19113652.
10
Psychometric properties of the SDM-Q-9 questionnaire for shared decision-making in multiple sclerosis: item response theory modelling and confirmatory factor analysis.用于多发性硬化症共同决策的SDM-Q-9问卷的心理测量特性:项目反应理论建模与验证性因素分析
Health Qual Life Outcomes. 2017 Apr 22;15(1):79. doi: 10.1186/s12955-017-0656-2.