﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Society of Diabetic Nephropathy Prevention</PublisherName>
      <JournalTitle>Journal of Nephropathology</JournalTitle>
      <Issn>2251-8363</Issn>
      <Volume>6</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2017</Year>
        <Month>07</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Association of Endothelin-1 rs5370 G&gt;T gene polymorphism with the risk of nephrotic syndrome in children</ArticleTitle>
    <FirstPage>138</FirstPage>
    <LastPage>143</LastPage>
    <ELocationID EIdType="doi">10.15171/jnp.2017.24</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Hashemi</LastName>
      </Author>
      <Author>
        <FirstName>Simin</FirstName>
        <LastName>Sadeghi-Bojd</LastName>
      </Author>
      <Author>
        <FirstName>Soheib</FirstName>
        <LastName>Aryanezhad</LastName>
      </Author>
      <Author>
        <FirstName>Maryam</FirstName>
        <LastName>Rezaei</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.15171/jnp.2017.24</ArticleId>
    </ArticleIdList>
    <History>
    </History>
    <Abstract>Background: Primary nephrotic syndrome (NS) is a common kidney disease in children. Objectives: The present study was aimed to investigate whether rs5370 G&gt;T (lys198Asn) genetic variant of endothelin-1 (ET-1) is involved in the susceptibility to NS. Patients and Methods: This case-control study was performed on 138 patients with NS and 150 healthy children. Genomic DNA was extracted from whole blood using salting out method. Polymorphism of the ET-1 rs5370 G&gt;T (lys198Asn) polymorphism detected by T-ARMS-PCR as well as PCR-RFLP method. Results: The results showed that the genotype and allelic frequencies of the ET-1 rs5370 G&gt;T variant were not significantly different between cases and controls. Furthermore, subgroup analysis showed that rs5370 G&gt;T variant was not associated with gender of patients. In NS patients the genotype was not associated with cholesterol, triglyceride, total protein and albumin levels. Conclusions: In conclusion, our findings indicate that ET-1 rs5370 G&gt;T is not associated with NS. Further studies with larger sample sizes and different ethnicities are required to validate our findings.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Nephrotic syndrome</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Endothelin-1</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Gene polymorphism</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>