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Published in: BMC Clinical Pathology 1/2009

Open Access 01-12-2009 | Research article

Matrix metalloproteinases in subjects with type 1 diabetes

Authors: Sedegheh Gharagozlian, Katja Svennevig, Hans-Jacob Bangstad, Jan-Olof Winberg, Svein Olav Kolset

Published in: BMC Clinical Pathology | Issue 1/2009

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Abstract

Background

Nephropathy is serious complication of diabetes. We have previously shown that level of the proteoglycan syndecan-1 in blood is associated with ultrastructural kidney changes in young persons with type 1 diabetes. Dysregulation of matrix metalloproteinases (MMPs) and tissue inhibitors of matrix metalloproteinases (TIMPs) may contribute to the development of nephropathy. The aim of this study was to investigate if the levels of MMPs in blood samples are potential markers of early nephropathy in type 1 diabetes.

Methods

Blood samples were collected from type 1 diabetes patients after 11 years of diabetes (n = 15) and healthy volunteers (n = 12) and stored at ÷80°C until measurement. Levels and activities of serum MMP-2, MMP-9, TIMP-1 and TIMP- 2 were analyzed and compared to those of control individuals using ELISA, SDS-PAGE gelatin zymography, and Western blot analysis.

Results

The serum levels of both MMP-9 and MMP-2 were significantly higher in subjects with type 1 diabetes, compared to controls (p = 0.016 and p = 0.008 respectively). Western blotting revealed no differences between the two groups in the levels of TIMP-1 or TIMP-2, respectively.

Conclusion

Our MMP analysis of serum from a limited number of patients with type 1 diabetes suggest that such analysis is potentially useful as markers in studies of people at risk of progression to chronic kidney disease.
Appendix
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Metadata
Title
Matrix metalloproteinases in subjects with type 1 diabetes
Authors
Sedegheh Gharagozlian
Katja Svennevig
Hans-Jacob Bangstad
Jan-Olof Winberg
Svein Olav Kolset
Publication date
01-12-2009
Publisher
BioMed Central
Published in
BMC Clinical Pathology / Issue 1/2009
Electronic ISSN: 1472-6890
DOI
https://doi.org/10.1186/1472-6890-9-7

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