Key result
Hypercholesterolemia is linked to ~175% higher endothelial microparticle counts, which inversely correlate with EDV.
Why the study?
Endothelial microparticles are elevated in cardiovascular diseases, but their comparison in hypercholesterolemia versus healthy controls and correlation with endothelium-dependent vasodilation required evaluation.
Are endothelial microparticles elevated in hypercholesterolemia and do they correlate with endothelial dysfunction?
Case-Control (n=88)
Are endothelial microparticles elevated in hypercholesterolemia and do they correlate with endothelial dysfunction?
Absolute Event Rate: 57.16% vs 20.78%
p-value: p=<0.001
Endothelial microparticles are significantly elevated in patients with hypercholesterolemia and correlate inversely with endothelium-dependent vasodilation, highlighting their potential as biomarkers for endothelial dysfunction.
EMPs may indicate endothelial dysfunction in hypercholesterolemia; hypothesis-generating for biomarker use, needs prospective validation.
Background and Objectives: Endothelial microparticles (EMP) particularly CD31+/42−/AV+, CD144+/AV+ and CD62e+/AV+ have been reported as having increased in cardiovascular-related diseases, making them potential biomarkers for endothelial dysfunction. This study aimed to compare these EMPs in patients with hypercholesterolemia and healthy controls and to correlate their levels with endothelium-dependent vasodilation (EDV) assessed via pulse wave analysis (PWA); an established method of assessing endothelial function. Materials and Methods: EMPs from 88 subjects (44 hypercholesterolemia patients and 44 controls) were quantified from whole blood using flow cytometry analysis. Endothelial function was determined using PWA combined with pharmacological challenge. Results: CD31+/42−/AV+ (3.45 ± 4.74 count/µL vs. 1.33 ± 4.40 count/µL; p = 0.03), CD144+/AV+ (7.37 ± 12.66 count/µL vs. 1.42 ± 1.71 count/µL; p = 0.003) and CD62e+/AV+ (57.16 ± 56.22 count/µL vs. 20.78 ± 11.04 count/µL; p < 0.001) were significantly elevated in the hypercholesterolemic group compared with the controls, respectively. There was a significant inverse moderate correlation between all circulating EMPs and EDV: CD31+/42−/AV+ (r = −0.36, p = 0.001), CD144+/AV+ (r = −0.37, p = 0.001) and CD62e+/AV+ (r = −0.35, p = 0.002). Conclusions: All EMPs were raised in the patients with hypercholesterolemia, and these values correlated with the established method of assessing endothelial function.
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Ibrahim et al. (2022) conducted a case-control in Hypercholesterolemia (n=88). Endothelial microparticles, including CD62e+/AV+, were significantly elevated in hypercholesterolemia patients versus controls (57.16 vs 20.78 count/µL; p<0.001) and inversely correlated with EDV.
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