To evaluate ultrasound enthesitis response in psoriatic arthritis

  • Research type

    Research Study

  • Full title

    An observational study evaluating the utility of ultrasound (US) confirmed enthesitis as a prognostic marker for response to biologic therapy in psoriatic arthritis (PsA).

  • IRAS ID

    242450

  • Contact name

    Madeleine Rooney

  • Contact email

    m.rooney@qub.ac.uk

  • Sponsor organisation

    Belfast Health and Social Care Trust, Reserach Goverance

  • Duration of Study in the UK

    1 years, 8 months, 29 days

  • Research summary

    The purpose of this project is to assess enthesitis in a cohort of Psoriatic Arthritis patients and how they respond to the biologic treatment available. Enthesitis is defined as inflammation at the insertion of the tendons, ligaments, and capsules into bone and is one of the hallmarks of Psoriatic Arthritis. It is an understudied aspect of the disease and ultrasound scanning has been shown to an effective and easily accessible tool to assess enthesitis. We have a range of treatment option in psoriatic arthritis but a key issue is that we have no way of telling which biologic drug will work for which patient and this can as a result be an expensive random process.

    A new medication available called secukinumab, which is a Interleukin 17 inhibitor is now approved as a first line agent for Psoriatic Arthritis once they have failed conventional disease modifying oral treatment. Clinical trials have suggested that both Secukinumab and the Anti TNF therapies are effective in treating enthesitis but this has not been assessed by ultrasound scoring in PsA.

    The aim of this observational study is to assess patients once they are approved for biologic treatment, with both clinical and ultrasound scoring systems. We aim to recruit 100 patients who are to commence on both Anti TNF and Secukinumab treatment, reviewing them prior to going on treatment and then at 4 months use repeating the same clinical and ultrasound assessment.

    This study will aim to clarify, in a cohort of active PsA patients, what is the prevalence of US confirmed enthesitis, what happens to these scores after biologic treatment, does this correlate with clinical scores and can enthesitis then serve as a prognostic tool in predicting response in patients receiving their biologic therapy.

  • REC name

    West Midlands - South Birmingham Research Ethics Committee

  • REC reference

    18/WM/0369

  • Date of REC Opinion

    14 Dec 2018

  • REC opinion

    Further Information Favourable Opinion