Dobutamine Stress Echocardiography in LF/LG Aortic Stenosis and Wild-type Transthyretin Amyloid Cardiomyopathy

Aortic Stenosis Clinical Trial

— DobAttrAS  

Official title:

Utility of Dobutamine Stress Echocardiography in the Diagnosis of Severe Aortic Stenosis in Patients With Low-flow Low-gradient and Co-exiting Wild-type Transthyretin Amyloid Cardiomyopathy

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06372301
• Other study ID #: 1-10-72-179-23
• Status: Recruiting
• Phase: N/A
• Start date: April 2, 2024
• Est. completion date: April 1, 2026

Study information

• Verified date: April 2024
• Source: Aarhus University Hospital Skejby
• Contact: Ali Hussein Jaber Mejren
• Phone: +4591651848
• Email: alimej[@]clin.au.dk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this prospective clinical study is improve the diagnosis of Low-flow low-gradient aortic stenosis (LF/LG AS), in patients with co-existing wild-type transthyretin cardiac amyloidosis (ATTRwt). The main question it aims to answer is whether the classic dobutamine-stress echocardiography can be used to determine AS severity in patients with ATTRwt and LF/LG AS This question will be tried to answer by comparing dobutamine stress echocardiography, with the invasively measured aortic valve area (which is considered as the gold standard).

In addition we aim to assess the degree of myocardial fibrosis and amyloid infiltration, assessed by light microscopy and cardiac magnetic resonance (CMRI) and evaluation of myocyte mitochondrial function by high resolution respirometry and their relation to AS severity and hemodynamic response to dobutamine.

Description:

Study protocol

A- Baseline assessment: The following will be measured:

• Blood pressure and heart rate.

• ECG.

• Standard echocardiography.

• Dobutamine stress echocardiography.

B- Catheterization laboratory: The participant will be transferred to the catheterization laboratory after about 1.5-hour recovery period after the end of dobutamine stress echocardiography. The following will be done in the following order:

• Right heart catheterization and endomyocardial biopsies.

• Left heart catheterization.

• Dobutamine challenge: Infusion of increasing dobutamine dosages, with simultaneous invasive measurements.

• Removal of left and right heart catheters: The catheters will be removed after 5 minutes recovery after dobutamine challenge.

C- Observation: The participant will then be transferred to our out-patient hospital for observation and the participant is expected to be discharged after 2 hours of observation, if no complications arise.

D- CMRI: All the participants will be evaluated with CMRI for estimation of LV mass, T-1 values, and extracellular volume (ECV). This will be scheduled for a separate visit.

Investigations and procedures

1. Dobutamine Challenges

Dobutamine challenge will be performed two times at the trial day. The first dobutamine challenge will be performed immediately after the baseline echocardiographic examination. The second dobutamine challenge will be performed no earlier than 2 hours later at the catherization laboratory as described below. Dobutamine, known for its brief half-life of approximately 2 minutes, ensures that its effects diminish rapidly, and the specified two-hour interval guarantees that its influence has subsided.

A ramp dobutamine infusion will be performed with a stepwise dobutamine dosage increase (dosages: 2,3,5,10,20 ug/kg/min). Dobutamine dosage will only be increased to 40 ug/kg/min in patients with ongoing beta-blocker treatment to ensure an appropriate dobutamine response.

The first dobutamine challenge with echocardiography: Blood pressure, heart rate, and standard echocardiography images will be obtained before the infusion start, at each infusion stage, and during the recovery period after the infusion is omitted. The projected aortic valve area (AVAproj.) is calculated by using the simplified formula:

AVAproj =AVArest + " AVApeak- AVArest" /"Qpeak-Qrest" " x (250- Qrest)

Q is defined as the transvalvular flow rate = SV/Ejection time. SV is calculated by the LVOTVTI x LVOTarea. Ejection time is measured by CW-Doppler of the valve profile.

The second dobutamine challenge with invasive measurements: This will be performed at the catheterization laboratory after the insertion of right and left heart catheters. There must be a minimum of 2 hours between the two dobutamine challenges. Blood pressure, heart rate, and pressure and flow measurements will be obtained before the infusion start, at each infusion stage, and during the recovery period after the infusion is omitted. AVA will be estimated at rest and at each dobutamine dose level using Gorlin formula.The abovementioned equation for AVAproj. will be also used to calculate AVAproj. from the invasive measurements.

2. Endomyocardial biopsies and biobank Before the right and left heart catheterization are initiated, three endomyocardial biopsies will be taken from the interventricular septum, through the internal jugular vein access (or femoral vein). The first biopsy is for evaluation of mitochondrial function by high resolution respirometry. The other two biopsies are for semi-quantitative evaluation of fibrosis and amyloid infiltration by standard diagnostic light microscopy at the department of pathology at Aarhus University Hospital. Any residual tissue from the first biopsy (to respirometry) will be destroyed after completing the analysis. The biopsies for light microscopy will be prepared, analyzed, and stored in clinical biobank according to the standard clinical practice at the department of pathology.

3. High Resolution Respirometry Biopsies used for high resolution respirometry are analyzed immediately after being taken. High resolution respirometry is performed at the unit of Clinical Research, Department of Cardiology at Aarhus University Hospital. The procedure is standard in the department.

4. Cardiac Magnetic Resonance Imaging (CMRI) CMRI scan will be performed to assess LV mass, fibrosis (assessed as late gadolinium enhancement), ECV assessed using T1-mapping, LV volume, left and right ventricular ejection fraction and strain mapping analysis. Gadolinium-based contrast will not be administered to participants with an estimated Glomerular Filtration Rate (eGFR) < 30 ml/min/1,73 m2 due to the risk of adverse effects.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 24
• Est. completion date: April 1, 2026
• Est. primary completion date: November 1, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 65 Years and older

Eligibility

Inclusion Criteria:

1. ATTRwt, diagnosis confirmed by 99mtc-3,3-Diphosphono-1,2-Propanodicarboxylic Acid (DPD) scintigraphy, genetic testing, and/or endomyocardial biopsy.

2. Symptomatic patients (New York Heart Association > class I) treated with loop diuretics.

3. LF/LG AS: Defined as, aortic valve area = 1 cm2 and mean gradient < 40 mmHg, and SVI =35 ml/m2.

4. Age = 65 years.

5. Oral and written informed consent.

Exclusion Criteria:

1. Other significant valvular disease.

2. Known severe coronary artery diseases: left main stem stenosis or 3-vessel disease, or recent acute myocardial infarction (< 4 weeks).

3. Contraindications to the use of dobutamine: Known allergy to dobutamine or sulfite, phaeochromocytoma or ventricular tachycardia (VT).

Related Conditions & MeSH terms

• Amyloidosis
• Aortic Stenosis
• Aortic Valve Stenosis
• Cardiomyopathies
• Constriction, Pathologic
• Transthyretin Amyloid Cardiomyopathy

Intervention

Diagnostic Test:
• Dobutamine stress echocardiography
Patients will be investigated with dobutamine stress echocardiography (increasing doses of dobutamine infusion and simulatneous echocardiogarphic evaluation) to assess aortic valve area and projected aortic valve area.

Locations

Country	Name	City	State
Denmark	Department of Cardiology, Aarhus University Hospital	Aarhus

Sponsors (1)

Lead Sponsor	Collaborator
Steen Hvitfeldt Poulsen

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The correlation between echocardiography derived projected aortic valve area (AVAproj) and invasively assessed AVAproj under dobutamine infusion.		Evaluated at the end of dobutamine infusion.
Secondary	Correlation between echocardiography derived AVA and invasively assessed AVA at rest and at different dobutamine infusion levels.		Evaluated at rest, at every dobutamine dose-level, and at the end of infusion.
Secondary	Increase of SVI, LV ejection fraction and LV-global longitudinal strain of 10 % during maximal dobutamine stimulation.		Evaluated at the end of dobutamine infusion.
Secondary	Correlation between echo- and invasive measured SVI.		Evaluated at the end of dobutamine infusion.
Secondary	Degree of myocardial fibrosis, amyloid infiltration and mitochondrial dysfunction and its relation to AS severity and hemodynamic response to dobutamine		CMRI would be performed within a max of 2 months from the trial day.
Secondary	Reduction of mean pulmonary artery wedge pressure and/or mean pulmonary artery pressure by 10 %.		Evaluated at the end of dobutamine infusion.
Secondary	Complication rate and symptomatic side effects during dobutamine challenge		Evaluated after couple of days after trial day with dobutamine infusion.