AIM: To investigate ENDRA rs5333 gene polymorphism distribution in idiopathic nephrotic syndrome (INS) and to analyze their association with response to steroid therapy, and biochemical markers of INS.
SUBJECTS & METHODS: The PCR-restriction fragment length polymorphism was used to analyze ENDRA rs5333 polymorphism in 100 children with idiopathic nephrotic syndrome (INS) and 100 healthy children. Plasma endothelin-1 were measured by ELISA.
RESULTS: The ENDRA rs5333 gene polymorphism was not associated with risk of INS. The frequency of minor allele (C) was significantly higher in the steroid resistant nephrotic syndrome group than the steroid sensitive group. The CC and TC mutant variants were associated with higher plasma levels of cholesterol, albumin, urea and 24-h urinary protein, but were not associated with risk of hypertension. The endothelin-1 plasma level was higher in INS than control and in steroid resistant nephrotic syndrome group when compared with steroid sensitive group cases.
CONCLUSION: The ENDRA rs5333 gene polymorphism may be associated with genetic predisposition to steroid resistance in INS Egyptian children.
Research Department	
              
          Research Journal	
              Pharmacogenomics Journal 2019;20(3):133-141.IF  2.265
          Research Member	
          
      Research Publisher	
              NULL
          Research Rank	
              1
          Research Vol	
              NULL
          Research Website	
              NULL
          Research Year	
              2019
          Research_Pages	
              NULL
          Research Abstract	
              
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