﻿<?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>2</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2013</Year>
        <Month>04</Month>
        <DAY>05</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Protective effect of selenium on cisplatin induced nephrotoxicity: A double-blind controlled randomized clinical trial</ArticleTitle>
    <FirstPage>129</FirstPage>
    <LastPage>134</LastPage>
    <ELocationID EIdType="doi">10.12860/JNP.2013.21</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Ali</FirstName>
        <LastName>Ghorbani</LastName>
      </Author>
      <Author>
        <FirstName>Bita</FirstName>
        <LastName>Omidvar</LastName>
      </Author>
      <Author>
        <FirstName>Abazar</FirstName>
        <LastName>Parsi</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.12860/JNP.2013.21</ArticleId>
    </ArticleIdList>
    <History>
    </History>
    <Abstract>Background: Renal injury is common following cisplatin infusion. Some agents have been used to attenuate cisplatin nephrotoxicity. However, except hydration, none of them has been proved to be effective. Objective: In this study selenium as an antioxidant supplement was tested on cisplatin induced renal injury. Patients and Methods: 122 cancerous patients (85 male and 37 female; age range of 14 to 82 years old) were enrolled to receive chemotherapy regimens consisting cisplatin. They were allocated into two groups using a random number list . Investigators, patients and analyzers all, were blinded in allocation by using sealed opaque envelopes. Intervention group received a single 400 mcg selenium tablet and patients in control group took a placebo tablet which was similar with selenium preparation in color, weight, shape and taste. Primary end points were an increase in plasma creatinine above 1.5 mg/dl in men and 1.4mg/dl in women, or increase of plasma creatinine more than 50% from baseline or urine flow rate less than 0.5 ml/kg/h. Creatinine level was measured initially and on the 5th day after cisplatin therapy. Results: There was no difference in cumulative dose of cisplatin between the groups (p=0.54). There were not evidences of acute renal failure (ARF) in cases. While, among placebo group, 7 patients had criteria of acute kidney injury. Conclusions: selenium could probably prevent cisplatin-induced acute kidney injury, when it is added to hydration therapy in cancerous patients.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Nephropathy</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Cisplatin</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Selenium</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Renal failure</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>