Horm Metab Res 2008; 40(6): 381-385
DOI: 10.1055/s-2008-1062746
Original Basic

© Georg Thieme Verlag KG Stuttgart · New York

Lipocalin-2: Development, Analytical Characterization, and Clinical Testing of a New ELISA

D. Stejskal 1 , 2 , M. Karpíšek 3 , V. Humenanska 4 , Z. Hanulova 4 , P. Stejskal 5 , P. Kusnierova 1 , M. Petzel 6
  • 1Department of Laboratory Medicine and Department of Medicine, Šternberk Hospital, Šternberk, Czech Republic
  • 2Institute of Medical Chemistry and Biochemistry, Faculty of Medicine and Dentistry, Palacký University Olomouc, Czech Republic
  • 3Institute of Human Pharmacology and Toxicology, Faculty of Pharmaceutical Sciences, Veterinary and Pharmaceutical University Brno, Czech Republic
  • 4Gnosis s.r.o., Slovakia
  • 5Department of Functional Anthropology and Physiology , Faculty of Physical Culture, Palacky University Olomouc, Czech Republic
  • 6Department of Gynecology, Faculty Hospital Ostrava Poruba, Czech Republic
Further Information

Publication History

received 02.07.2007

accepted 26.10.2007

Publication Date:
31 March 2008 (online)

Abstract

Lipocalin-2 (also known as neutrophil gelatinase-associated lipocalin [NGAL]) has been described as a promising marker of metabolic syndrome associated with inflammation. The aim of our work was to develop an assay for the determination of lipocalin-2 in human serum and to investigate its levels in healthy volunteers and donors suffering from metabolic syndrome. We also conducted a pilot study on individuals with metabolic syndrome and on healthy probands and measured lipocalin-2 in these individuals. We developed and evaluated the sandwich ELISA method for the quantitative determination of human lipocalin-2 in serum samples. We measured blood pressure, waist circumference, serum cholesterol, triglycerides, HDL cholesterol, LDL cholesterol, insulin, glucose, creatinine, hs-CRP, and adiponectin and calculated the BMI and Quicki insulin sensitivity index. In the study on 153 healthy volunteers, we showed that sex and age are not determinative for lipocalin-2 serum values. Furthermore, we tested 45 individuals with metabolic syndrome; values of lipocalin-2 did not differ (78.8 vs. 80.0 μg/l, p=0.56) from the data of healthy individuals from the first study. Neither group differed with regard to sex or age. Lipocalin-2 correlated with alanine aminotransferase (ALT) (r=-0.3, p<0.01) aspartate aminotransferase (AST) (r=-0.3, p<0.01), cholesterol (r=-0.21, p=0.047), creatinine (r=0.19, p=0.05), and high-sensitivity C-reactive protein (hs-CRP) (r=0.22, p=0.036). No significant correlation was found between serum lipocalin-2 and BMI, waist circumference, blood pressure, triglycerides, HDL, Quicki, or the number of metabolic syndrome components. When study patients with metabolic syndrome were further stratified according to the number of components of metabolic syndrome, serum concentrations of lipocalin-2 did not differ. The results presented demonstrate the analytical competence of the lipocalin-2 assay. However, we assumed that lipocalin-2 is not a routinely usable marker of metabolic syndrome or obesity. The association between serum lipocalin-2 and obesity or metabolic syndrome was not validated in our study.

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Correspondence

D. StejskalMD, PhD, Assoc. Prof. 

Department of Laboratory Medicine

Šternberk Hospital

Jivavska 20

78516 Šternberk

Czech Republic

Phone: +42/058/508 73 08

Fax: +42/058/508 71 31

Email: david.stejskal@nemstbk.cz