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Right ventricular myocardial deoxygenation in patients with pulmonary artery hypertension
Right ventricular myocardial deoxygenation in patients with pulmonary artery hypertension
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Right ventricular myocardial deoxygenation in patients with pulmonary artery hypertension
Right ventricular myocardial deoxygenation in patients with pulmonary artery hypertension
Journal Article

Right ventricular myocardial deoxygenation in patients with pulmonary artery hypertension

2021
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Overview
Background In pulmonary arterial hypertension (PAH), progressive right ventricular (RV) dysfunction is believed to be largely secondary to RV ischaemia. A recent pilot study has demonstrated the feasibility of Oxygen-sensitive (OS) cardiovascular magnetic resonance (CMR) to detect in-vivo RV myocardial oxygenation. The aims of the present study therefore, were to assess the prevalence of RV myocardial ischaemia and relationship with RV myocardial interstitial changes in PAH patients with non-obstructive coronaries, and corelate with functional and haemodynamic parameters. Methods We prospectively recruited 42 patients with right heart catheter (RHC) proven PAH and 11 healthy age matched controls. The CMR examination involved standard functional imaging, OS-CMR imaging and native T1 mapping. An ΔOS-CMR signal intensity (SI) index (stress/rest signal intensity) was acquired at RV anterior, RV free-wall and RV inferior segments. T1 maps were acquired using Shortened Modified Look-Locker Inversion recovery (ShMOLLI) at the inferior RV segment. Results The inferior RV ΔOS-CMR SI index was significantly lower in PAH patients compared with healthy controls (9.5 (– 7.4–42.8) vs 12.5 (9–24.6)%, p  = 0.02). The inferior RV ΔOS-CMR SI had a significant correlation to RV inferior wall thickness (r = – 0.7, p  < 0.001) and RHC mean pulmonary artery pressure (mPAP) (r = – 0.4, p  = 0.02). Compared to healthy controls, patients with PAH had higher native T1 in the inferior RV wall: 1303 (1107–1612) vs 1232 (1159–1288)ms, p  = 0.049. In addition, there was a significant difference in the inferior RV T1 values between the idiopathic PAH and systemic sclerosis associated PAH patients: 1242 (1107–1612) vs 1386 (1219–1552)ms, p  = 0.007. Conclusion Blunted OS-CMR SI suggests the presence of in-vivo microvascular RV dysfunction in PAH patients. The native T1 in the inferior RV segments is significantly increased in the PAH patients, particularly among the systemic sclerosis associated PAH group.
Publisher
BioMed Central,BioMed Central Ltd,Elsevier
Subject

Adenosine

/ Aged

/ Angiology

/ Bias

/ Cardiac magnetic resonance (CMR)

/ Cardiac patients

/ Cardiology

/ Cardiovascular disease

/ Care and treatment

/ Case-Control Studies

/ Catheters

/ Coronary Circulation

/ Coronary microvascular dysfunction

/ Coronary vessels

/ Deoxygenation

/ Edema

/ Ejection fraction

/ Feasibility studies

/ Female

/ Heart

/ Heart rate

/ Hemodynamics

/ Hemoglobin

/ Humans

/ Hypertension

/ Imaging

/ Ischemia

/ Magnetic resonance

/ Magnetic Resonance Imaging, Cine

/ Male

/ Medicine

/ Medicine & Public Health

/ Microcirculation

/ Microvasculature

/ Middle Aged

/ Myocardial Ischemia - diagnostic imaging

/ Myocardial Ischemia - etiology

/ Myocardial Ischemia - metabolism

/ Myocardial Ischemia - physiopathology

/ Myocardium - metabolism

/ Oxygen - metabolism

/ Oxygen-sensitive cardiac magnetic resonance

/ Oxygenation

/ Prospective Studies

/ Pulmonary Arterial Hypertension - complications

/ Pulmonary Arterial Hypertension - diagnostic imaging

/ Pulmonary Arterial Hypertension - metabolism

/ Pulmonary Arterial Hypertension - physiopathology

/ Pulmonary arteries

/ Pulmonary artery

/ Pulmonary artery hypertension

/ Pulmonary hypertension

/ Radiology

/ Right ventricle

/ Scleroderma

/ Scleroderma (Disease)

/ Segments

/ South Australia

/ Systemic scleroderma

/ Systemic sclerosis

/ T1 mapping

/ Values

/ Ventricle

/ Ventricular Dysfunction, Right - diagnostic imaging

/ Ventricular Dysfunction, Right - etiology

/ Ventricular Dysfunction, Right - metabolism

/ Ventricular Dysfunction, Right - physiopathology

/ Ventricular Function, Left

/ Ventricular Function, Right

/ Wall thickness