Why the study?
LV function impairment and pathophysiology in coronary slow flow remain controversial, and the relationship between pulsatile arterial load and layer-specific LV contractility needed investigation.
Does coronary slow flow impair layer-specific left ventricular strain and alter pulsatile arterial load compared to normal coronary angiography?
Does coronary slow flow impair layer-specific left ventricular strain and alter pulsatile arterial load compared to normal coronary angiography?
Patients with coronary slow flow exhibit impaired endocardial and mid-myocardial longitudinal strain, which is associated with greater pulsatile arterial load.
Suggests subclinical myocardial dysfunction in coronary slow flow may link to increased arterial stiffness; leaves open whether.
Previous studies reported a controversial left ventricular (LV) function impairment and pathophysiology in patients with coronary slow flow (CSF). Greater arterial load has been shown to increase aortic impedance and endothelial shear stress, potentially affecting coronary anatomy and function. We investigated LV systolic function by a new layer-specific strain technology and assessed the association between pulsatile arterial load and contractility.A total of 70 patients with CSF and 50 controls with normal coronary angiography were included in the study. Layer-specific longitudinal and circumferential strains were assessed from endocardium, mid-myocardium, and epicardium (global longitudinal strain (GLS)-endo, GLS-mid, GLS-epi and GCS-endo, GCS-mid, GCS-epi) by two-dimensional speckle tracking imaging (2D-STI). Pulsatile arterial load was estimated by indexed arterial compliance (ACI). Layer-specific GLS showed a decreasing gradient from the endocardium to the epicardium in both the controls and CSF group. GLS-endo and GLS-mid in the CSF group were significantly lower than the control group (all P < 0.05). Layer-specific longitudinal strain showed a good correlation with the number of affected coronary arteries (all P < 0.05) and the mean thrombolysis in the myocardial infarction frame count (TFC) (all P < 0.05). ACI was lower in patients with CSF (P = 0.005), and ACI was correlated negatively with layer-specific GLS (all P < 0.05).Layer-specific evaluation of the LV provides an understanding of the layer-specific properties of the LV wall and the possible process of the LV impairment in patients with CSF. Greater pulsatile arterial load, as manifested by a lower ACI, is coupled with worse LV longitudinal function in patients with CSF.
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Shi et al. (2019) studied this question.
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