| Literature DB >> 31243138 |
Daniel Castle1,2, Ray Wynford-Thomas1,2, Sam Loveless1,2, Emily Bentley2, Owain W Howell3, Emma C Tallantyre4,2.
Abstract
Long-term outcomes in multiple sclerosis (MS) are highly varied and treatment with disease-modifying therapies carries significant risks. Finding tissue biomarkers that can predict clinical outcomes would be valuable in individualising treatment decisions for people with MS. Several candidate biomarkers-reflecting inflammation, neurodegeneration and glial pathophysiology-show promise for predicting outcomes. However, many candidates still require validation in cohorts with long-term follow-up and evaluation for their independent contribution in predicting outcome when models are adjusted for known demographic, clinical and radiological predictors. Given the complexity of MS pathophysiology, heterogeneous panels comprising a combination of biomarkers that encompass the various aspects of neurodegenerative, glial and immune pathology seen in MS, may enhance future predictions of outcome. © Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: biomarkers; multiple sclerosis (ms); neurofilament; outcome; pathophysiology
Year: 2019 PMID: 31243138 DOI: 10.1136/practneurol-2018-002000
Source DB: PubMed Journal: Pract Neurol ISSN: 1474-7758