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Published on: October 12, 2017
Dysfunctional HDL takes its Toll on the endothelial glycocalyx
1Bristol Renal, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Insights
Patients with end-stage renal disease develop dysfunctional high-density lipoprotein cholesterol, leading to endothelial glycocalyx degradation. This novel finding links kidney failure to cardiovascular disease by identifying an early molecular insult.
Area of Science:
- Cardiovascular Science
- Nephrology
- Molecular Biology
Background:
- End-stage renal disease (ESRD) patients face elevated cardiovascular disease (CVD) mortality.
- Traditional CVD risk factors do not fully explain this heightened risk.
Purpose of the Study:
- To investigate the role of dysfunctional high-density lipoprotein cholesterol (HDL-C) in ESRD-related CVD.
- To explore the link between ESRD, HDL-C dysfunction, and endothelial glycocalyx integrity.
Main Methods:
- The study by Hesse et al. proposes a mechanism involving HDL-C generated in ESRD patients.
- This dysfunctional HDL-C is suggested to impact the endothelial glycocalyx.
Main Results:
- Dysfunctional HDL-C in ESRD patients is implicated in endothelial glycocalyx degradation.
- Glycocalyx degradation is identified as a potential early step in atheroma formation.
Conclusions:
- Dysfunctional HDL-C in ESRD patients contributes to endothelial damage.
- This research proposes a novel pathway connecting renal failure to cardiovascular pathology via glycocalyx degradation.
Abstract:
Patients with end-stage renal disease have a high risk of dying from cardiovascular disease that cannot be explained solely by traditional cardiovascular disease risk factors. Hesse et al. suggest that dysfunctional high-density lipoprotein cholesterol generated in patients with end-stage renal disease causes endothelial glycocalyx degradation. Glycocalyx degradation may represent one of the earliest insults leading to atheroma formation, and so this work suggests a novel link between renal failure and cardiovascular disease.
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