Bosentan for Mild Pulmonary Vascular Disease in Asd Patients.

1. INTRODUCTION AND RATIONALE 1.1 MEDICAL BACKGROUND Atrial septal defect (ASD) represents approximately 10% of all congenital heart diseases and is the third most common form of congenital heart defect. The incidence of congenital heart disease in Belgium is 1%, with ASD accounting for 25% of the cases (Data from the database of congenital heart diseases UZ Leuven.) Characterized by a free communication between the left and the right atrium, it may take the form of an ostium secundum defect (in the region of the fossa ovalis); an ostium primum defect (in the lower part of the atrial septum and associated with mitral regurgitation) or a sinus venosus defect (in the upper atrial septum and associated with anomalous drainage of one or more pulmonary veins) Patients with atrial septal defect (ASD) initially present with a left-to-right shunt, which may cause elevated pulmonary artery pressures at rest and/or during exercise. However, this persistently elevated pulmonary blood-flow also causes progressive lesions of the pulmonary vasculature, as first described by Heath and Edwards. The earlier stages present with medial hypertrophy and/or intimal proliferation and are largely reversible after closure of the defect. Later stages, however, are irriversible: the origin of pulmonary arterial hypertension (PAH). Eventually, this volume and pressure overload of the right heart may lead to heart failure and/or arrhythmias. As PVR exceeds systemic resistance, the shunt is reversed (right-to-left shunt) leading to systemic arterial desaturation (and the related consequences: polyglobulia, hyperuricemia, decreased renal function and abnormal coagulation): the Eisenmenger syndrome (ES). When occlusive fibrotic lesions have developed later in life, closure of the ASD, although still feasible, may not result in complete normalization of pulmonary artery pressures. Moreover, it has been shown that closure after the age of 40 years is associated with worse outcome. It has been suggested that an abnormal increase in pulmonary artery pressures during exercise reflects mild pulmonary vascular disease. However, pulmonary artery pressures are defined by both cardiac output and pulmonary vascular resistance. During exercise, the relationship between pulmonary artery pressures and cardiac output is slightly curvilinear because of a natural distensibility of the pulmonary arterioles. Using bicycle stress echocardiography, pulmonary vascular resistance can be estimated either as a ratio of pulmonary artery pressure and cardiac output at each stage (total PVR) or by using linear regression analysis of the pressure-flow plots (dynamic PVR). Prognosis of patients with unrepaired ASDs is thought to be shortened and repair can avoid right ventricular (RV) failure, pulmonary hypertension, thrombo-embolic events and atrial dysrrhythmias. So, when the defect is discovered early, an ASD is usually closed in childhood, unless the defect is considered not to be clinical significant. Sometimes, as most patients with an isolated ASD are asymptomatic during childhood, an ASD comes to medical attention at an older age. Patients with a corrected ASD have a poorer prognosis than patients in a control group, especially in the presence of PAH, which confers an eightfold increased probability of functional limitations. In the Euroheart survey PAH was present in 12% of patients with a closed ASD. As PAH is a progressive disease, early diagnosis and treatment may improve outcome in these patients. A first analysis of data obtained from the registry of ASD showed that in the transcatheter closed ASD patients, mPAP was the only independent predictor of atrial arrhythmia after ASD repair. Moreover, our first prospective study showed that it is possible to identify patients with mild pulmonary vascular disease using stress echocardiography and that patients with an ASD closed at later age were unable to decrease pulmonary vascular resistance during exercise, resulting in a higher pulmonary vascular resistance at peak exercise when compared to a control group. This was reflected in a steeper pressure-flow plot when compared to healthy controls. Endothelin has shown to influence vasomotor tone, especially during exercise. Moreover, Faoro et al showed that bosentan decreased pulmonary vascular resistance as assessed with pressure-flow plots during hypoxia. Therefore, this study was designed to evaluate the effect of an dual endothelin receptor antagonist on total pulmonary vascular resistance during exercise in an older ASD patient population. 1.2 DRUG PROFILE Mechanism of action Bosentan is a dual endothelin receptor antagonist (ERA) with affinity for both endothelin A and B (ET-A and ET-B) receptors. Bosentan decreases both pulmonary and systemic vascular resistance resulting in increased cardiac output without increasing heart rate. The neurohormone endothelin-1 (ET-1) is one of the most potent vasoconstrictors known and can also promote fibrosis, cell proliferation, cardiac hypertrophy, and remodeling and is pro-inflammatory. These effects are mediated by endothelin binding to ET-A and ET-B receptors located in the endothelium and vascular smooth muscle cells. ET-1 concentrations in tissues and plasma are increased in several cardiovascular disorders and connective tissue diseases, including pulmonary arterial hypertension, scleroderma, acute and chronic heart failure, myocardial ischaemia, systemic hypertension and atherosclerosis, suggesting a pathogenic role of ET-1 in these diseases. In pulmonary arterial hypertension and heart failure, in the absence of endothelin receptor antagonism, elevated ET-1 concentrations are strongly correlated with the severity and prognosis of these diseases. Bosentan competes with the binding of ET-1 and other ET peptides to both ET-A and ET-B receptors, with a slightly higher affinity for ET-A receptors (Ki = 4.1-43 nM) than for ET-B receptors (Ki = 38-730 nM). Bosentan specifically antagonises ET receptors and does not bind to other receptors. 1.3 RATIONALE FOR PERFORMING THE STUDY Although an ASD seems an easily correctable defect, patients with a repaired ASD have a poorer prognosis than patients in a control group, especially in the presence of PAH, which confers an eightfold increased probability of functional limitations. In the Euroheart survey PAH was present in 12% of patients with a closed ASD. Whether it is useful to treat mild to moderate pulmonary vascular disease after repair of an ASD with specific PAH treatment in order to have a positive effect on exercise capacity and even outcome outcome still needs to be evaluated. As outlined in section 1.1, the investigators were able to identify patients with mild pulmonary vascular disease using bicycle exercise echocardiography. Patients with an ASD repaired after the age of 40 years appeared to have higher PVR when compared to healthy controls. Moreover, in older patients a higher mPAP at diagnosis was an independent predictor for the occurrence of late atrial arrhythmias. Therefore, the present study will investigate whether bosentan has a beneficial effect on PVR as measured with bicycle stress echocardiography in patients with repaired ASD and WHO FC II mild pulmonary vascular disease using dynamic PVR as a surrogate endpoint. 1.3.1 DOSE AND POSOLOGY Treatment will be initiated at a dose of 62.5 mg twice daily for 4 weeks and then increased to the maintenance dose of 125 mg twice daily for 12 weeks. Dosage in elderly patients: No dosage adjustment in required in patients over the age of 65 years.
2. STUDY OBJECTIVES The primary efficacy objective is to assess the efficacy of the dual active endothelin receptor antagonist bosentan in patients with WHO functional class II mild to moderate PAH after surgical or interventional closure of an ASD .
3. STUDY DESIGN

This is a prospective, monocentric, randomised, double-blind, placebo-controlled, pilot study to evaluate the efficacy of dual active endothelin receptor antagonist bosentan in patients with WHO FC II, mild pulmonary vascular disease after ASD repair.

4 STATISTICAL METHODS AND DETERMINATION OF SAMPLE SIZE

The null hypothesis of the study is that in patients receiving specific PAH treatment no change in PVR is observed. This trial aims to demonstrate to efficacy of bosentan to lower PVR as assessed by bicycle exercise echocardiography in patients with surgically or transcatheter closed ASD.

5 RANDOMISATION

Patients will be randomly assigned to treatment groups with equal probability of assignment to each treatment arm (allocation ratio 1:1). The randomisation schedule will be generated using validated software. The investigators will remain blinded to the randomisation schedule until after the final database is locked. The randomisation schedule will be examined only if required by an emergency. Any such break should be documented clearly.

6 SAMPLE SIZE CALCULATION

As the study design is considered as a pilot trial, it primarily aims at defining means and standard deviations in both treatment arms in order to allow for future sample size calculations.