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Publication Date:
June 2008
ISSN:
1437-4331
DOI:
10.1515/CCLM.2008.171

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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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Urinary fructose-1,6-bisphosphatase activity as a marker of the damage to the renal proximal tubules in children with idiopathic nephrotic syndrome

Alina Kępka1 / Sławomir Dariusz Szajda2 / Anna Stypułkowska3 / Napoleon Waszkiewicz4 / Anna Jankowska5 / Sylwia Chojnowska6 / Krzysztof Zwierz7

1Department of Laboratory Diagnostics of the Institute “Pomnik-Centrum Zdrowia Dziecka”, Warsaw, Poland

2Department of Pharmaceutical Biochemistry, Medical University of Bialystok, Bialystok, Poland

3Department of Pharmaceutical Biochemistry, Medical University of Bialystok, Bialystok, Poland

4Department of Psychiatry, Medical University of Bialystok, Bialystok, Poland

5Department of Pedodontics, Medical University of Bialystok, Bialystok, Poland

6Department of Pharmaceutical Biochemistry, Medical University of Bialystok, Bialystok, Poland

7Department of Pharmaceutical Biochemistry, Medical University of Bialystok, Bialystok, Poland

Corresponding author: Sławomir D. Szajda, PhD, Assistant Professor, Department of Pharmaceutical Biochemistry, Medical University, Mickiewicza Str. 2A, 15-230 Bialystok, Poland Phone: +48-85-748-5690/748-5691,

Citation Information: Clinical Chemistry and Laboratory Medicine. Volume 46, Issue 6, Pages 831–835, ISSN (Online) 1437-4331, ISSN (Print) 1434-6621, DOI: 10.1515/CCLM.2008.171, June 2008

Publication History:
Received:
2007-01-01
Accepted:
2008-02-02
Published Online:
2008-06-09

Abstract

Background: Disturbances in the function of renal proximal tubules increase the activity of several enzymes in urine. Among them is fructose-1,6-bisphosphatase (FBP-1), the key enzyme of gluconeogenesis normally present in the renal convoluted, and to smaller degree, proximal renal tubular cells cytosol. FBP-1 activity in urine and serum was used for evaluation of the degree of graft ischemia during human kidney transplantation. The aim of our present research was to determine FBP-1 activity in urine as an indicator of damage to renal proximal tubules in children with idiopathic nephrotic syndrome (INS).

Methods: We evaluated the excretion of FBP-1 into urine of 21 children (10 girls and 11 boys) with INS, aged from 10 to 15 years and 30 healthy children (14 girls and 16 boys), aged from 2 to 15 years. FBP-1 activity was determined by the Latzko and Gibbs method. Creatinine (mg%) in urine and blood serum was measured by the Jaffe method in Larsen modification. Protein in blood serum was determined by the biuret method (g/L), and albumin (mg%) by the Young method. Proteinuria in the urine collected over 24 h was measured with the Exton turbidimetric method by Tomaszewski with modification and expressed in mg/kg body weight/24 h.

Results: In the urine of 30 healthy children, FBP-1 activity was in the range from 0–1.74 μmol FPB/h/mmol of creatinine. In 43% of the healthy children, FBP-1 activity in urine was not detectable. In the period of intensive proteinuria during the INS in children, FBP-1 activity and protein concentrations in urine were significantly higher than in the control group (p<0.0008 and p<0.0001, respectively). In the urine of children with active INS, we observed a very weak negative linear correlation between protein concentration and FBP-1 activity (r=−0.5018, p=0.067). After treatment with Encorton (prednisone), FBP-1 activity and protein concentration in urine dropped to values of the control group.

Conclusions: “The overload” of proximal renal tubules by proteins in children with INS releases FBP-1 into urine. FBP-1 activity in urine may therefore be considered as a marker of damage to the proximal renal tubules in children with INS.

Clin Chem Lab Med 2008;46:831–5.

Keywords: fructose-1,6-bisphosphatase (FBP-1); idiopathic nephrotic syndrome; renal proximal tubules

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