Why the study?
Anthracyclines may affect the vascular system and heart in childhood cancer survivors, but left ventricular-arterial coupling had never been investigated in this setting.
Does prior anthracycline chemotherapy alter left ventricular-arterial coupling and endothelial function in childhood cancer survivors compared to healthy controls?
Does prior anthracycline chemotherapy alter left ventricular-arterial coupling and endothelial function in childhood cancer survivors compared to healthy controls?
Three-dimensional echocardiography may detect early subclinical impairment in left ventricular-arterial coupling in childhood cancer survivors exposed to anthracyclines before changes in conventional parameters or endothelial function occur.
3D parameters may flag early LVAC changes in survivors undetected conventionally; leaves open prospective validation before surveillance use.
Background: Cardiovascular (CV) diseases are a cause of increased long-term morbidity and mortality in childhood cancer survivors (CCSs) treated with anthracyclines. These drugs may affect not only the heart, but also the vascular system. Left ventricular-arterial coupling (LVAC) represents a reliable parameter of altered ventricular and vascular performance, with validated prognostic value and never investigated in this setting. Aim of this study was to assess, in CCSs and matched controls, LVAC changes, performed with different echocardiographic modalities, and their relationship with endothelial function. Methods: Twenty survivors treated with anthracyclines for childhood malignancies and a matched control group of 20 healthy subjects were enrolled. Arterial elastance (Ea), end-systolic elastance (Ees), Ea/Ees ratio, as well as three-dimensional (3D) LVAC (assessed by measurement of End Systolic Volume [ESV]/Stroke Volume [SV] ratio) were performed at rest. Endothelial function was evaluated by measurement of flow-mediated dilatation (FMD) of the brachial artery. Results: 3D SV and 3D ESV/SV ratio resulted respectively significantly lower and higher in CCSs than in controls, while Ea, Ees and Ea/Ees ratio were not different among groups. A positive correlation between 3D ESV/SV ratio and cumulative anthracycline doses, as well as with time after drug exposure were also found. Mean FMD was similar in CCSs and controls (8.45 ± 1.79 versus 9.41 ± 3.41, p = 0.34). Conclusions: In conclusion, conventional LVAC parameters were not shown to be significantly different between CCSs and controls; however, 3D SV and LVAC were significantly impaired in our population. In these patients, endothelial function was comparable to controls. Larger validation studies are therefore needed.
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Camilli et al. (2023) studied this question.
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