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Endothelial Glycocalyx Damage Coincides With Microalbuminuria in Type 1 Diabetes

Max NieuwdorpDepartment of Vascular Medicine, Academic Medical Center, Amsterdam, the NetherlandsHans L. MooijDepartment of Vascular Medicine, Academic Medical Center, Amsterdam, the NetherlandsJojanneke KroonDepartment of Vascular Medicine, Academic Medical Center, Amsterdam, the NetherlandsBektaş AtaseverDepartment of Clinical Physiology, Academic Medical Center, Amsterdam, the NetherlandsJos A. E. SpaanDepartment of Medical Physics, Academic Medical Center, Amsterdam, the NetherlandsCan İnceDepartment of Clinical Physiology, Academic Medical Center, Amsterdam, the NetherlandsF. HollemanDepartment of Internal Medicine, Academic Medical Center, Amsterdam, the NetherlandsMichaëla DiamantDepartment of Endocrinology, Diabetes Center, VU University Medical Center, Amsterdam, the NetherlandsRobert J. HeineDepartment of Endocrinology, Diabetes Center, VU University Medical Center, Amsterdam, the NetherlandsJ. B. L. HoekstraDepartment of Internal Medicine, Academic Medical Center, Amsterdam, the NetherlandsJohn J.P. KasteleinDepartment of Vascular Medicine, Academic Medical Center, Amsterdam, the NetherlandsErik S.G. StroesDepartment of Vascular Medicine, Academic Medical Center, Amsterdam, the NetherlandsHans VinkDepartment of Medical Physics, Academic Medical Center, Amsterdam, the Netherlands
2006en
ABI

Аннотация

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 microm, 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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