In this issue of the journal, Sciagrà et al. report on the use of 13 N-ammonia ( 13 NH 3 ) to recognize transmural perfusion abnormalities in patients with hypertrophic cardiomyopathy (HCM) [1]. The authors developed a method to quantify absolute blood flow in the subendocardial and subepicardial layers. This paper comes after a series of studies using 15 Owater (H 2 15 O) with cardiac positron emission tomography (PET) to split mean transmural myocardial perfusion into two layers (subendocardial and subepicardial) and conducted in patients having normal or increased left ventricular (LV) myocardial wall thickness: HCM, coronary artery disease (CAD), aortic stenosis and healthy controls [2][3][4][5][6]. The study by Sciagrà et al. is of particular interest because it broadens the scope of application of cardiac PET to the use of a more widely available myocardial perfusion PET radiotracer 13 NH 3 for splitting mean transmural absolute myocardial wall perfusion into subendocardial and subepicardial components.This study provides the opportunity to raise some interesting points concerning cardiac PET and its potential for exploring new frontiers by splitting mean myocardial wall quantitative parameters into two layers.
Clinical need to go beyond mean transmural myocardial parametersImaging the LV myocardium is of particular interest in different clinical situations, i.e. ischaemic heart disease, heart failure, hypertension, hypertrophic cardiomyopathies, myocarditis, amyloidosis, sarcoidosis and systemic sclerosis, etc.Since a few years now, the feasibility of high spatial resolution cardiac imaging has afforded the possibility of fractiona t i ng t h e LV m y oc ar di u m i nt o d i ff er en t l a ye r s (subendocardium, midwall, subepicardium), particularly with late contrast-enhanced (LCE) cardiac MRI. This latter encountered great clinical success due to its significant additional clinical value in different situations, i.e. subendocardial LCE in subendocardial myocardial infarction, subepicardial and midwall LCE in myocarditis, preferential subendocardial LCE in amyloidosis, subendocardial or midmyocardial LCE in systemic sclerosis, subepicardial and midwall LCE of the inferolateral wall in Churg-Strauss syndrome, etc.In addition to MRI, echocardiography and multidetector computed tomography are also engaged in this race of splitting LV mean transmural myocardial measurements into different layers, particularly the subendocardial, midwall and subepicardial components. These high spatial resolution techniques are actively investigating each layer of the myocardium with the hope that at the very early steps of disease these fractional measurements would allow more precise comprehension of its pathophysiology, facilitate its earlier detection, add incremental prognostic value, guide treatment and evaluate treatment efficacy. As will be discussed below, cardiac PET is also actively engaged in this quest. In concordance with its actual lower spatial resolution, cardiac PET is for the time being splitting the myoca...