Studying remyelination in nerves with electrophysiology

  • Research type

    Research Study

  • Full title

    Studying progressive remyelination in nerves by grading electrophysiological recovery

  • IRAS ID

    284097

  • Contact name

    Alasdair Coles

  • Contact email

    ajc1020@medschl.cam.ac.uk

  • Sponsor organisation

    Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge

  • Duration of Study in the UK

    10 years, 0 months, 3 days

  • Research summary

    The greatest unmet need in multiple sclerosis (MS) are treatments which delay, or reverse disability. Now, drugs are being discovered that can promote regeneration of the lining of nerves in MS. The problem is uncertainty in the optimum test to measure this effect in people, over the course of a clinical trial.

    One technique that has proved increasingly useful in this respect is a simple and safe non-invasive test of the speed of conduction along the optical pathway: the visual evoked potential (VEP). The full-field VEP has previously been deployed in clinical trials, and now recent research has indicated that multi-focal VEP (MF-VEP) might be more sensitive and robust to detect remyelination. Similarly, another test, this time looking at eye movements, has also been advocated to be an effective method to study nerve repair and regeneration. This test of eye movements (called saccades) can be measured using a non-invasive portable saccadometer.

    However, there is a knowledge gap in that it is not known exactly how these measures are affected by the natural course of multiple sclerosis, how they change with time following a relapse (MS flare) affecting the eyes (optic neuritis), and how durable changes that we observe can be. It is also not known how these changes compare with other illnesses that affect the visual pathway. This is essential as researchers will be increasingly relying on these tests to monitor the effects of novel therapies in the setting of clinical trials.

    We will characterise abnormalities in the VEPs and saccades of MS patients compared with controls at different timepoints over the course of 1-2 years; a smaller subgroup will be invited to continue to 5 years. We will be able to use this information to better determine how to employ these tests in a robust, rigorous fashion, within clinical trials.

  • REC name

    Wales REC 7

  • REC reference

    20/WA/0294

  • Date of REC Opinion

    12 Nov 2020

  • REC opinion

    Further Information Favourable Opinion