Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (4)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Hörstrup, J. H.
Right arrow Articles by Eckardt, K.-U.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hörstrup, J. H.
Right arrow Articles by Eckardt, K.-U.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nephrol Dial Transplant (2002) 17: 1005-1013
© 2002 European Renal Association-European Dialysis and Transplant Association

Elevation of serum and urine levels of TIMP-1 and tenascin in patients with renal disease

Jan Henrik Hörstrup1, Mathias Gehrmann2, Birgit Schneider1, Angela Plöger3, Peter Froese1, Thea Schirop1, Dieter Kampf1, Ulrich Frei1, Rainer Neumann4 and Kai-Uwe Eckardt1,

1 Department of Nephrology and Medical Intensive Care, Charité, Campus Virchow-Klinikum, Berlin, 2 Bayer Research Centre, Uerdingen, 3 Department of Nephrology, Gilead II Hospital, Bielefeld and 4 Bayer Vital GmbH, Leverkusen, Germany

Background. Chronic kidney disease is characterized by increased synthesis and inhibited destruction of collagenous and non-collagenous matrix proteins. Elevation of collagen fragments has been demonstrated in the serum and urine of patients with renal disease, but the dynamics of renal matrix deposition remain difficult to determine.

Methods. To obtain a further insight into renal matrix metabolism we have assessed whether serum and urine concentrations of the non-collagenous protein, tenascin, and of the tissue inhibitor of metalloproteinases 1 (TIMP-1) are altered in association with renal disease. Serum and urine concentrations of both proteins were determined using a newly developed magnetic particle enzyme immunoassay and were compared with levels of N-terminal procollagen III-peptide (PIIINP) and related to the degree of renal failure and proteinuria.

Results. Circulating levels of tenascin and TIMP-1 were moderately, but significantly, higher in patients with chronic renal disease (n=54; mean creatinine clearance, 62 ml/min) than in healthy controls (n=176). Urine concentrations per mg creatinine of tenascin and TIMP-1 were significantly lower than serum levels, but were on average six- and 18-fold higher, respectively, in patients with renal disease than in controls. Urinary concentrations increased with progressive reduction in renal function, but were unrelated to proteinuria. TIMP-1 concentrations in urine correlated with tenascin, which is compatible with the impact of TIMP-1 on the accumulation of matrix proteins. The concentrations of proteins measured did not differ depending on the aetiology of renal disease.

Conclusion. Urinary concentrations of tenascin and TIMP-1 are elevated in association with renal disease and may reflect specific aspects of renal fibrosis.

Keywords: procollagen III-peptide; renal fibrosis; serum; tenascin; tissue inhibitor of metalloproteinases-1; urine

Correspondence and offprint requests to: K.-U. Eckardt, MD, Department of Nephrology and Medical Intensive Care, Charité, Humboldt Universität, Campus Virchow Klinikum, Augustenburger Platz 1, D-13353 Berlin, Germany. Email: kai\|[hyphen]\|uwe.eckardt{at}charite.de


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Toxicol SciHome page
M. Sieber, D. Hoffmann, M. Adler, V. S. Vaidya, M. Clement, J. V. Bonventre, N. Zidek, E. Rached, A. Amberg, J. J. Callanan, et al.
Comparative Analysis of Novel Noninvasive Renal Biomarkers and Metabonomic Changes in a Rat Model of Gentamicin Nephrotoxicity
Toxicol. Sci., June 1, 2009; 109(2): 336 - 349.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
J. M. Catania, G. Chen, and A. R. Parrish
Role of matrix metalloproteinases in renal pathophysiologies
Am J Physiol Renal Physiol, March 1, 2007; 292(3): F905 - F911.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
J.-S. F. Sanders, H. van Goor, R. Hanemaaijer, C. G. M. Kallenberg, and C. A. Stegeman
Renal expression of matrix metalloproteinases in human ANCA-associated glomerulonephritis
Nephrol. Dial. Transplant., June 1, 2004; 19(6): 1412 - 1419.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.