<?xml version="1.0"?>
<Articles JournalTitle="Acta Medica Iranica">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Acta Medica Iranica</JournalTitle>
      <Issn>0044-6025</Issn>
      <Volume>51</Volume>
      <Issue>11</Issue>
      <PubDate PubStatus="epublish">
        <Year>2013</Year>
        <Month>11</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">UDP-Glucuronosyltransferase Promoter Polymorphism in Iranian Neonates with Idiopathic Hyperbilirubinemia</title>
    <FirstPage>789</FirstPage>
    <LastPage>792</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mahbod</FirstName>
        <LastName>Kaveh</LastName>
        <affiliation locale="en_US">Department of Neonatology, Bahrami Children Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Tahereh</FirstName>
        <LastName>Esmailnia</LastName>
        <affiliation locale="en_US">Department of Neonatology, Vali-e-Asr Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Fatemeh</FirstName>
        <LastName>Nayeri</LastName>
        <affiliation locale="en_US">Department of Neonatology, Vali-e-Asr Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Firoozeh</FirstName>
        <LastName>Nili</LastName>
        <affiliation locale="en_US">Department of Neonatology, Vali-e-Asr Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Fatemeh</FirstName>
        <LastName>Davari Tanha</LastName>
        <affiliation locale="en_US">Department of Obstetrics &amp;Gynecology , Women&#x2019;s Hospital, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mahsa</FirstName>
        <LastName>Ghajarzdeh</LastName>
        <affiliation locale="en_US">Brain and Spinal Injury Repair Research Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>11</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">To determine the association between polymorphism of UGT1A1 gene and idiopathic hyperbilirubinemia in Iranian neonates. Fifty neonates with idiopathic hyperbilirubinemia and Serum total bilirubin (STB) more that 15mg/dl and 50 neonates with idiopathic hyperbilirubinemia and Serum total bilirubin (STB) less than 15mg/dl enrolled in this study. Thymine-adenine (TA)&#xA0; repeats in the promoter region of UGT1A1 gene investigated by means of&#xA0; polymerase- chain reaction (PCR) DNA sequencing. Demographic characteristics did not differ significantly between groups while STB was higher in case group (17.5&#xB1;1.9 vs. 10.4&#xB1;1.8, p value&lt;0.001). Among one hundred neonates evaluated in this study, TA6/6, TA6/7 and TA7/7 genotypes found in 52%, 42% and 6%, totally. TA6/7 and TA7/7 genotypes observed in case group more than the control group (P&lt;0.001). STB levels were significantly higher in cases with TA6/7 and TA7/7 genotype pattern (P&lt;0.001). Heterozygous and variant homozygous genotypes of the promoter region of UGT1A1 gene in healthy Iranian neonates with idiopathic hyperbilirubinemia should be considered.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/4347</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/4347/4487</pdf_url>
  </Article>
</Articles>
