TY - JOUR
TI - Endothelial glycocalyx integrity in oncological patients
AU - Keramida, K.
AU - Thymis, J.
AU - Anastasiou, M.
AU - Katogiannis, K.
AU - Kotsantis, I.
AU - Economopoulou, P.
AU - Pappa, V.
AU - Tsirigotis, P.
AU - Bistola, V.
AU - Thodi, M.
AU - Psyrri, A.
AU - Filippatos, G.
AU - Ikonomidis, I.
JO - International Journal of Cardiology
PY - 2022
VL - 360
TODO - null
SP - 62-67
PB - Elsevier Ireland Ltd
SN - 0167-5273
TODO - 10.1016/j.ijcard.2022.05.010
TODO - arterial stiffness;  cardiotoxicity;  glycocalyx;  human;  microvasculature;  pathology;  pulse wave, Cardiotoxicity;  Glycocalyx;  Humans;  Microvessels;  Pulse Wave Analysis;  Vascular Stiffness
TODO - Background: Cancer is associated with early changes in the cardiovascular system (CV) before overt cardiotoxicity. Endothelial dysfunction is induced by chemotherapeutic regimens but there is no data for endothelial glycocalyx in cancer. Methods: Sixty-four patients with cancer (65.6% with solid tumors and 34.4% with hematological malignancies) and 32 controls from the outpatient cardiology clinic were included in the study. The perfused boundary region (PBR) of the sublingual arterial microvessels, Pulse Wave Velocity (PWV) and augmentation index (AI) were measured. A standard transthoracic echocardiogram plus assessment of global longitudinal strain (GLS) of all cardiac chambers were performed. Results: There was no difference in the baseline profile (age, sex, smoking, hypertension, diabetes, hyperlipidemia and coronary artery disease) and in the echocardiographic parameters between the two groups, with the exception of left atrial volume (33.3 ± 13 in cancer patients vs 27.6 ± 6.5 ml/m2 in controls). PBR 5–25 and PBR 20–25 were significantly increased in cancer patients vs controls (2.11 ± 0.36 vs 1.97 ± 0.21 μm, p = 0.025 and 2.65 ± 0.48 vs 2.40 ± 0.36 μm, p = 0.012, respectively). Endothelial glycocalyx thickness impairment was independent of traditional CV risk factors and anticancer therapy, but proportional to disease stage (r = 0.337, p = 0.044). However, there was no difference in arterial stiffness between the two groups (PWV 10.74 ± 4.11 vs 11.26 ± 3.38 m/s, p = 0.539 and AI 11.28 ± 28.87 vs 15.38 ± 18.8 %, p = 0.470). Conclusions: Endothelial function as assessed by endothelial glycocalyx thickness is significantly impaired in cancer patients without overt cardiotoxicity. This implies that PBR might be useful for the early assessment of microvascular and endothelial toxicity of cancer. © 2022 Elsevier B.V.
ER -