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

Vermersch, P; Berger, T; Gold, R; Lukas, C; Rovira, A; Meesen, B; Chard, D; ... Trojano, M; + view all (2016) The clinical perspective: How to personalise treatment in MS and how may biomarkers including imaging contribute to this? MULTIPLE SCLEROSIS JOURNAL , 22 (2) pp. 18-33. 10.1177/1352458516650739. Green open access

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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.

Type: Article
Title: The clinical perspective: How to personalise treatment in MS and how may biomarkers including imaging contribute to this?
Open access status: An open access version is available from UCL Discovery
DOI: 10.1177/1352458516650739
Publisher version: http://doi.org/10.1177/1352458516650739
Language: English
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences, Neurosciences & Neurology, Biological markers, disease progression, drug-related side effects and adverse reactions, magnetic resonance imaging, multiple sclerosis, treatment response, PROGRESSIVE MULTIPLE-SCLEROSIS, LONG-TERM DISABILITY, MAGNIMS CONSENSUS GUIDELINES, MAGNETIZATION-TRANSFER RATIO, INTERFERON-BETA, BRAIN ATROPHY, NEUROFILAMENT LIGHT, GLATIRAMER ACETATE, NATURAL-HISTORY, MULTIFOCAL LEUKOENCEPHALOPATHY
UCL classification: UCL
UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Neuroinflammation
URI: https://discovery.ucl.ac.uk/id/eprint/1508511
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