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2014 | 61 | 1 | 67-75

Article title

Polymorphic variants of MIF gene and prognosis in steroid therapy in children with idiopathic nephrotic syndrome

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EN

Abstracts

EN
Nephrotic syndrome (NS) is the most common reason of proteinuria in children and can be caused by the pathology of renal glomeruli. Steroid therapy is typically used in this disorder. It has been shown that MIF is a cytokine which counteracts the immunosuppressive properties of glucocorticoids. The aim of this study was looking for a correlation between MIF polymorphisms and genetic susceptibility to steroid resistance in children with INS (Idiopathic NS). Methods: The study was performed in 71 patients with INS including SRNS (steroid resistance nephrotic syndrome) (41) and SSNS (steroid sensitive nephrotic syndrome) (30) and in 30 control subjects. We employed Sanger sequencing and capillary electrophoresis. Linkage disequilibrium was made using Haploview and PHASE. Results: We didn't observe a statistical significance between SNPs detected in patients with INS and controls. Our studies revealed statistical significance for two polymorphisms: rs2070767C > T and rs2000466T > G between patients with SRNS and SSNS. The results for rs34383331T > A are close to being statistically significant. Statistical significance was revealed for CATT5/CATT6 genotype in SRNS group vs SSNS group (OR=4.604, 95%CI=1.356-15.632, p=0.0168). We found that the frequency of 5/X-CATT genotype compared with X/X-CATT genotype was significantly higher in SRNS patients vs SSNS (OR=3.167, 95%CI=1.046-9.585, p=0.0426). In linkage disequilibrium analysis we didn't show involvement in susceptibility to INS and steroid sensitive phenotype. Conclusions: Our results suggest that the role of MIF polymorphisms in the susceptibility to positive response to steroid therapy is still unresolved. It indicates that MIF may be involved in indirect and complex molecular mechanisms of steroid activity in hormone-dependent metabolic pathways in children with INS. Because of ambiguous findings, pleiotropic features of this cytokine require that more research should be undertaken.

Year

Volume

61

Issue

1

Pages

67-75

Physical description

Dates

published
2014
received
2013-06-03
revised
2013-11-25
accepted
2014-01-22
(unknown)
2014-03-18

Contributors

  • Department of Histology and Embryology, Poznan University of Medical Sciences, Poland
  • Department of Pediatric Cardiology and Nephrology, Poznan University of Medical Sciences, Poland
  • Department of Histology and Embryology, Poznan University of Medical Sciences, Poland
  • Laboratory of Molecular and Cell Biology, Department of Pulmonology, Pediatric Allergy and Clinical Immunology, Poznan University of Medical Sciences, Poland
  • Department of Histology and Embryology, Poznan University of Medical Sciences, Poland

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Document Type

Publication order reference

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bwmeta1.element.bwnjournal-article-abpv61p67kz
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