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Publication Date:
January 2012
ISSN:
1437-4331
DOI:
10.1515/cclm.2011.881

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Clinical Chemistry and Laboratory Medicine (CCLM)

Published in Association with the International Federation of Clinical Chemistry and Laboratory Medicine and the European Federation of Clinical Chemistry and Laboratory Medicine

Editor-in-Chief: Plebani, Mario

Editorial Board Member: Lippi, Giuseppe / Gillery, Philippe / Kazmierczak, Steven / Lackner, Karl J. / Melichar, Bohuslav / Siest, Gérard / Whitfield, John B. / Abi Fadel, Marianne / Alvarez Menendez, Francisco V. / Azzazy, Hassan M.E. / Diamandis, Eleftherios P. / Eckardstein, Arnold / Favaloro, Emmanuel J. / Griesmacher, Andrea / Herrmann, Wolfgang / Hoffmann, Johannes J.M.L. / Hooijkaas, Herbert / Ichihara, Kiyoshi / Kaabachi, Naziha / Kim, Jeong-Ho / Korte, Wolfgang / Kroupis, Christos / Lai, Leslie Charles / Lam, Wai Kei Christopher / Marc, Janja / Miyoshi, Eiji / Özben, Tomris / Palicka, Vladimir / Panteghini, Mauro / Queralto, Jose M. / Scartezini, Marileia / Simundic, Ana-Maria / Tsongalis, Gregory J. / Wallemacq, Pierre E. / Yan, Shengkai / Young, Ian S. / Chiu, Rossa Wai Kwun / Ghosh, Debabrata / Kappelmayer, Janos / Lehmann, Sylvain / Sypniewska, Grazyna

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Increased IMPACT FACTOR 2011: 2.150
Rank 10 out of 32 in category Medical Laboratory Technology in the 2011 Thomson Reuters Journal Citation Report/Science Edition

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Extracellular matrix-associated (GAGs, CTGF), angiogenic (VEGF) and inflammatory factors (MCP-1, CD40, IFN-γ) in type 1 diabetes mellitus nephropathy

Olga Ellina1 / Antonios Chatzigeorgiou1, a / Sophia Kouyanou2 / Maria Lymberi1 / Christina Mylona-Karagianni3 / Emmanouil Tsouvalas3 / 1

1Department of Experimental Physiology, Medical School, National and Kapodistrian University of Athens, Athens, Greece

2Division of Genetics and Biotechnology, Department of Biology, National and Kapodistrian University of Athens, Athens, Greece

3Second Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, Panagiotis and Aglaia Kyriakou Pediatric Hospital, Athens, Greece

aA. Chatzigeorgiou asserts equal contribution and joint first authorship.

Corresponding author: Dr. Elli F. Kamper, Department of Experimental Physiology, Medical School, National and Kapodistrian University of Athens 75, M. Asias Str., GR-11527, Goudi, Athens, Greece Phone: +30-210-7462595, Fax: +30-210-7462594

Citation Information: Clinical Chemistry and Laboratory Medicine. Volume 50, Issue 1, Pages 167–174, ISSN (Online) 1437-4331, ISSN (Print) 1434-6621, DOI: 10.1515/cclm.2011.881, January 2012

Publication History:
Received:
2011-06-28
Accepted:
2011-09-06

Abstract

Background: The aim of the present study was to evaluate the role of extracellular matrix-associated glycosaminoglycans (GAGs), connective tissue growth factor (CTGF), angiogenic vascular endothelial growth factor (VEGF) and inflammatory factors (MCP-1, CD40, IFN-γ) in the development of diabetic nephropathy in type 1 diabetes (T1DM).

Methods: Plasma and urine samples from 30 T1DM patients and 20 healthy controls were used to measure the levels of CTGF, VEGF, MCP-1, CD40 and IFN-γ by ELISA. Plasma and urine GAGs were measured using a spectrophotometric method.

Results: Plasma levels of GAGs, CD40 and MCP-1 and urine levels of GAGs and CTGF were significantly elevated in normoalbuminuric T1DM patients. A tendency to higher plasma VEGF levels was found in patients compared to controls. The urine/plasma GAGs ratio of T1DM patients was almost similar to that of healthy subjects (HS), whereas the urine/plasma CTGF ratio was about three times greater in diabetic patients compared to HS.

Conclusions: Conclusively, increased GAGs and CTGF excretion are evident in T1DM normoalbuminuric juveniles, possibly reflecting early renal injury signs, before the initiation of albuminuria.

Keywords: connective tissue growth factor; diabetic nephro­pathy (DN); extracellular matrix (ECM); glycosaminoglycans (GAGs); inflammation; type 1 diabetes mellitus (T1DM)

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