4.5 Article

Impaired Endothelial Glycocalyx Predicts Adverse Outcome in Subjects Without Overt Cardiovascular Disease: a 6-Year Follow-up Study

Journal

JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH
Volume 15, Issue 4, Pages 890-902

Publisher

SPRINGER
DOI: 10.1007/s12265-021-10180-2

Keywords

Perfused boundary region; Glycocalyx; Primary prevention; Greek population; Prospective study; SCORE

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The study found that disturbance of glycocalyx integrity is related to increased cardiovascular risk. Higher PBRS-25 values predicted a higher risk for MACE, and adding PBRS-25 to predictive models improved their accuracy in predicting cardiovascular events. Glycocalyx integrity serves as an independent and additive predictor to traditional risk factors for MACE at a 6-year follow-up in individuals without cardiovascular disease.
We investigated whether disturbance of glycocalyx integrity is related with increased cardiovascular risk. In 600 healthy subjects, we measured perfused boundary region (PBR), a marker of glycocalyx integrity, in sublingual microvessels with diameter ranging 5-25 mu m using a dedicated camera (Sideview Darkfield Imaging). Increased PBR indicates reduced glycocalyx thickness. We prospectively monitored the occurrence of cardiovascular events (MACE-death, myocardial infarction, and stroke) during a 6-year follow-up. Fifty-seven MACE were documented. Increased values of PBRS-25 predicted higher risk for MACE in a model including sex, age, hyperlipidemia, diabetes, hypertension, smoking, family history of coronary disease, treatment with ACEi/ARBs, or lipid-lowering agents (hazard ratio (HR), 6.44, p = 0.011; net reclassification improvement (NRI), 28%; C-statistic: 0.761). PBRS-25 was an independent and additive predictor of outcome when added in a model including the European Heart SCORE, diabetes, family history of CAD, and medication (HR, 4.71; NRI: 39.7%, C-statistic from 0.653 to 0.693; p < 0.01). Glycocalyx integrity is an independent and additive predictor to risk factors for MACE at 6-year follow-up in individuals without cardiovascular disease.

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