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Updated: Apr 1, 2026

Assessment of Kidney Function in Mouse Models of Glomerular Disease
Published on: June 30, 2018
The glycocalyx--linking albuminuria with renal and cardiovascular disease
Ton J Rabelink1, Dick de Zeeuw2
1Department of Medicine, Division of Nephrology, Einthoven Laboratory for Experimental Vascular Medicine, LUMC, Leiden University Medical Centre, Netherlands.
Insights
Albuminuria, a marker of kidney disease, may actively worsen kidney and cardiovascular conditions by damaging the endothelial glycocalyx. Restoring this protective layer offers potential therapeutic targets for disease progression.
Area of Science:
- Nephrology
- Cardiology
- Vascular Biology
Background:
- Albuminuria is a common indicator of kidney disease progression.
- Endothelial damage, driven by factors like diabetes and hypertension, contributes to kidney and cardiovascular disease.
- The endothelial glycocalyx, a protective barrier, is crucial in preventing albumin filtration.
Purpose of the Study:
- To review mechanisms linking glycocalyx dysfunction to kidney injury.
- To explain the association between cardiovascular disease and albuminuria.
- To explore therapeutic potential for targeting glycocalyx dysfunction.
Main Methods:
- Review of existing literature on glycocalyx function and dysfunction.
- Examination of pathophysiological pathways.
- Analysis of clinical associations and therapeutic implications.
Main Results:
- Glycocalyx degradation leads to albuminuria and inflammation.
- Endothelial dysfunction is a key mechanism in albuminuria-related kidney and cardiovascular disease.
- Glycocalyx dysfunction appears to be reversible.
Conclusions:
- Glycocalyx dysfunction provides a framework for understanding albuminuria's role in disease progression.
- Targeting glycocalyx integrity presents novel therapeutic opportunities.
- Albuminuria may need to be re-evaluated as a clinical trial endpoint.
Abstract:
Albuminuria is commonly used as a marker of kidney disease progression, but some evidence suggests that albuminuria also contributes to disease progression by inducing renal injury in specific disease conditions. Studies have confirmed that in patients with cardiovascular risk factors, such as diabetes and hypertension, endothelial damage drives progression of kidney disease and cardiovascular disease. A key mechanism that contributes to this process is the loss of the glycocalyx--a polysaccharide gel that lines the luminal endothelial surface and that normally acts as a barrier against albumin filtration. Degradation of the glycocalyx in response to endothelial activation can lead to albuminuria and subsequent renal and vascular inflammation, thus providing a pathophysiological framework for the clinical association of albuminuria with renal and cardiovascular disease progression. In this Review, we examine the likely mechanisms by which glycocalyx dysfunction contributes to kidney injury and explains the link between cardiovascular disease and albuminuria. Evidence suggests that glycocalyx dysfunction is reversible, suggesting that these mechanisms could be considered as therapeutic targets to prevent the progression of renal and cardiovascular disease. This possibility enables the use of existing drugs in new ways, provides an opportunity to develop novel therapies, and indicates that albuminuria should be reconsidered as an end point in clinical trials.
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