TAKO MEMRI Version 1.0

  • Research type

    Research Study

  • Full title

    Manganese-enhanced Magnetic Resonance Imaging in Takotsubo Cardiomyopathy

  • IRAS ID

    348948

  • Contact name

    David Newby

  • Contact email

    d.e.newby@ed.ac.uk

  • Sponsor organisation

    University of Edinburgh

  • Duration of Study in the UK

    3 years, 0 months, 5 days

  • Research summary

    Takotsubo cardiomyopathy is a medical condition which presents similarly to a heart attack. It is usually caused by physical or emotional stress and typically affects women aged 50-74. It causes sudden severe impairment in heart muscle function, which was previously thought to get better in a matter of weeks. However, 1 in 10 patients will die in hospital and those that recover have substantially reduced long-term survival. There is no definitive treatment for takotsubo cardiomyopathy at present.

    Standard heart scans carried out in clinical care suggest that takotsubo cardiomyopathy gets better within a few weeks. However, we know that patients don't always feel better at this stage. We have previously demonstrated that performing an MRI scan of the heart using a special dye called manganese shows that changes in the heart muscle persist for months to years after the original diagnosis of takotsubo cardiomyopathy.

    We propose to assess the effects of established heart failure therapy on patients with takotsubo cardiomyopathy, specifically the effects this has on manganese-enhanced MRI scans.

    Participants will be divided into two study groups based on the timing of their diagnoses. Participants with a recent diagnosis less than 3 months ago will be allocated to receive Bisoprolol, Valsartan or no medication. Participants with a diagnosis more than 6 months ago will be allocated to receive Sacubitril/Valsartan or Dapaglifozin for 3 months then will change to the alternative medication for 3 months with a 1-month wash-out period in between.

    Participants will attend for study visits every few weeks-months to assess the effects of the medication. At the study visits they will undergo a range of investigations including the manganese-enhanced MRI scan, echocardiogram, ECG, walking test and blood tests. Furthermore, patients will undergo a clinical assessment by the study doctor and be asked to complete a symptom questionnaire.

  • REC name

    North of Scotland Research Ethics Committee 1

  • REC reference

    25/NS/0005

  • Date of REC Opinion

    12 Feb 2025

  • REC opinion

    Further Information Favourable Opinion