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Diabetes 55:1127-1132, 2006
DOI: 10.2337/diabetes.55.04.06.db05-1619
© 2006 by the American Diabetes Association
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Endothelial Glycocalyx Damage Coincides With Microalbuminuria in Type 1 Diabetes

Max Nieuwdorp1, Hans L. Mooij1, Jojanneke Kroon1, Bektas Atasever2, Jos A.E. Spaan3, Can Ince2, Frits Holleman4, Michaela Diamant5, Robert J. Heine5, Joost B.L. Hoekstra4, John J.P. Kastelein1, Erik S.G. Stroes1, and Hans Vink3

1 Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands
2 Department of Clinical Physiology, Academic Medical Center, Amsterdam, the Netherlands
3 Department of Medical Physics, Academic Medical Center, Amsterdam, the Netherlands
4 Department of Internal Medicine, Academic Medical Center, Amsterdam, the Netherlands
5 Department of Endocrinology, Diabetes Center, VU University Medical Center, Amsterdam, the Netherlands

Address correspondence and reprint requests to Erik Stroes, MD, PhD, Department of Vascular Medicine, Room F4.275, Academic Medical Center University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, Netherlands. E-mail: e.s.stroes{at}amc.uva.nl

Abbreviations: OPS, orthogonal polarization spectral

Chronic hyperglycemia underlies microvascular complications in patients with type 1 diabetes. The mechanisms leading to these vascular complications are not fully understood. Recently, we observed that acute hyperglycemia results in endothelial glycocalyx damage. To establish whether glycocalyx is associated with microvascular damage, we performed glycocalyx perturbation volume measurements in type 1 diabetic patients with microalbuminuria (DM1-MA group; n = 7), without microalbuminuria (DM1-NA group; n = 7), and in age-matched control subjects (CON; n = 7). Systemic glycocalyx volume was determined comparing intravascular distribution volume of a glycocalyx-permeable tracer (dextran 40) to that of a glycocalyx-impermeable tracer (labeled erythrocytes). Sublingual capillaries were visualized using orthogonal polarization spectral microscopy to estimate microvascular glycocalyx. Patients and control subjects were matched according to age and BMI. Glycocalyx volume decreased in a stepwise fashion from CON, DM1-NA, and finally DM1-MA subjects (1.5 ± 0.1, 0.8 ± 0.4, and 0.2 ± 0.1 l, respectively, P < 0.05). Microvascular glycocalyx in sublingual capillaries was also decreased in type 1 diabetes versus the control group (0.5 ± 0.1 vs. 0.9 ± 0.1 µm, P < 0.05). Plasma hyaluronan, a principal glycocalyx constituent, and hyaluronidase were increased in type 1 diabetes. In conclusion, type 1 diabetic patients are characterized by endothelial glycocalyx damage, the severity of which is increased in presence of microalbuminuria.


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