The Role of SGLT2i in Management of Moderate AS

Last updated: June 17, 2024
Sponsor: University of East Anglia
Overall Status: Active - Recruiting

Phase

2/3

Condition

N/A

Treatment

Empagliflozin 10 MG

Clinical Study ID

NCT06469645
R212199
  • Ages > 18
  • All Genders

Study Summary

Background:

The aortic valve is like a door in the heart that lets blood flow out to the body. Over time, this valve can get worn out and become too narrow, leading to a condition called aortic stenosis. When this happens, the heart has to work extra hard to push blood through the narrow valve to supply the body with what it needs. This extra effort can cause the heart muscle to become abnormally thick or to have fibrosis. For people with aortic stenosis, this can lead to more problems like feeling out of breath, chest pain, and even needing to go to the hospital. It also increases the risk of dying from heart issues. There is a type of medication called Sodium Glucose Cotransporter 2 (SGLT2) inhibitors, which has been studied in people with weak heart muscle. These medicines were found to help the heart work better and improve the pumping of blood around the body. This can be promising for patients with aortic stenosis because it might make the heart muscle stronger and protect it from damage.

Aim of research study:

The aim of this study is to investigate whether the use of the drug empagliflozin, an SGLT2 inhibitor, prevents the formation of fibrosis or the abnormal thickening of the heart muscle in patients with aortic stenosis. Using advanced imaging techniques (such as echocardiography and cardiovascular magnetic resonance), we intend to study their effect on the heart muscle of patients with aortic stenosis.

Study design:

Patients with moderate aortic stenosis will be invited for participation. Eligible consenting patients will have a baseline assessment with cardiac MRI scan, echocardiography, cardiopulmonary exercise test and validated quality of life questionnaires. They will then be randomised to receive either the SGLT2i for 6 months, or standard of care. All patients will undergo the same tests at 6 months. This way, we aim to investigate the potential changes in the heart muscle and whether the SGLT2 inhibitor prevents fibrosis or hypertrophy.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Moderate aortic stenosis (aortic valve peak velocity ≥ 3m/s or mean gradient 20-40mmHg, or Aortic valve area 1.0-1.5cm2)

  2. Age over 18 years

Exclusion

Exclusion Criteria:

  1. Severe aortic stenosis (aortic valve peak velocity ≥ 4m/s or mean > 40mmHg or Aorticvalve area < 1.0cm2) or planned cardiac surgery or likely need for surgery within 6months.

  2. Previous valve replacement

  3. Severe hypertension (systolic >180mmHg or diastolic >100mmHg)

  4. Acute pulmonary oedema or cardiogenic shock

  5. Coexisting other valvular lesion of more than moderate severit.

  6. Coexisting hypertrophic cardiomyopathy or amyloidosis with cardiac involvement

  7. Any contraindications to MRI scanning including eGFR <30ml/min/1.73m2

  8. Pregnancy or breast-feeding

  9. Concomitant SGLT2 inhibitor therapy

  10. Inability to receive SGLT2 inhibitor therapy

  11. History of diabetes type 1 or 2

  12. Severe peripheral vascular disease or non-healed leg ulcers

  13. Severe liver disease

  14. Rare hereditary problems of galactose intolerance, total lactase deficiency, orglucose-galactose malabsorption

Study Design

Total Participants: 104
Treatment Group(s): 1
Primary Treatment: Empagliflozin 10 MG
Phase: 2/3
Study Start date:
May 30, 2024
Estimated Completion Date:
February 28, 2026

Study Description

Background:

Aortic stenosis represents one of the commonest valvular heart diseases in the Western World. Studies have shown that as the valvular narrowing progresses, pathological left ventricular (LV) hypertrophy and fibrosis develop. This maladaptive left ventricular remodelling is associated with adverse events and worse long-term prognosis. Currently, there is no available medication to slow down or prevent these pathological processes occurring in aortic stenosis. Evidence from recent large randomised controlled trials have demonstrated that SGLT2 inhibitors have a significant positive impact on quality of life and cardiovascular outcomes of patients with heart failure. This is a result of complex mechanisms such as attenuation of cardiac myofibroblast activity and collagen remodelling. These could be proved to be very beneficial for patients with aortic stenosis since the left ventricular pathological changes occurring in aortic stenosis share similar pathways and mechanisms with heart failure.

Study aims and objectives:

The aims of this study are to assess if:

  • SGLT2 inhibitors can prevent or decelerate adverse myocardial remodelling and fibrosis.

  • SGLT2 inhibitors can improve the exercise tolerance and functional capacity of patients with aortic stenosis.

Methods:

Given that the use of SGLT2 inhibitors in aortic stenosis has not been investigated before, we aim to investigate the hypotheses with an early stage randomised controlled trial. For this, patients with moderate aortic stenosis identified in the outpatient cardiology clinic will be invited to participate. Management of moderate aortic stenosis is conservative with a 'watchful waiting' approach. The participants will be randomised either to usual conservative management or to the intervention group (use of SGLT2 inhibitor on top of regular medications). They will be assessed at baseline and at 6-months following initiation of the medication. Both appointments will include evaluation of symptoms (with the use of validated questionnaire) and functional capacity (cardiopulmonary exercise test), electrocardiogram and blood tests. An echocardiogram, a scan performed routinely on a yearly basis for all patients with moderate aortic stenosis, will also be performed at baseline and at completion of the 6 months' follow-up period to evaluate for myocardial hypertrophy and remodelling. Additionally, a cardiopulmonary exercise test and a cardiac magnetic resonance scan will be performed in these two timepoints to assess for myocardial remodelling and fibrosis.

Connect with a study center

  • Norfolk and Norwich University Hospital

    Norwich, Norfolk
    United Kingdom

    Active - Recruiting

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