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Increased α3-fucosylation of α1-acid glycoprotein in Type I diabetic patients is related to vascular function

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Abstract

Diabetic mellitus is attended by the development of endothelial dysfunction which is suggested to be accompanied with a chronic low-degree of inflammation. During a chronic hepatic inflammatory response, specific changes in glycosylation of the acute phase protein α1-acid glycoprotein (AGP) can be detected. In this report we studied the changes in glycosylation of AGP in more detail and evaluated the relation between a change in glycosylation of AGP and urinary albumin secretion in Type I diabetic patients. The glycosylation of AGP, studied by crossed affinity immunoelectrophoresis (CAIE) and high pH anion exchange chromatography with pulse amperometric detection (HPAEC-PAD), showed an increase in α3-fucosylation. Staining with an antibody against sialyl Lewisx (sLex) implied that part of the α3-fucosylation was present in a sLex-conformation. In the group of Type I diabetic patients with increased urinary albumin excretion, a significant increase in α3-fucosylation of AGP (p[emsp4 ]<[emsp4 ]0.0005) could be detected. Therefore, the increased α3-fucosylation of AGP can be used as an additional marker for the development of vascular complications in Type I diabetic patients.

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Poland, D.C.W., Schalkwijk, C.G., Stehouwer, C.D.A. et al. Increased α3-fucosylation of α1-acid glycoprotein in Type I diabetic patients is related to vascular function. Glycoconj J 18, 261–268 (2001). https://doi.org/10.1023/A:1012412908983

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  • DOI: https://doi.org/10.1023/A:1012412908983

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