<?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>55</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>08</Month>
        <Day>19</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Association of the Single Nucleotide Polymorphisms of the Genes Encoding IL-2 and IFN-&#x3B3; With Febrile Seizure</title>
    <FirstPage>354</FirstPage>
    <LastPage>359</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Amin</FirstName>
        <LastName>Shahrokhi</LastName>
        <affiliation locale="en_US">Pediatric Neurorehabilitation Research Center, The University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. AND Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Ameneh</FirstName>
        <LastName>Zare-Shahabadi</LastName>
        <affiliation locale="en_US">Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran. AND NeuroImmunology Research Association (NIRA), Universal Scientific Education and Research Network (USERN), Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Naeimi Poor</LastName>
        <affiliation locale="en_US">Noor Afshar Hospital, Iranian Red Crescent Society, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Firouzeh</FirstName>
        <LastName>Sajedi</LastName>
        <affiliation locale="en_US">Pediatric Neurorehabilitation Research Center, The University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Samaneh</FirstName>
        <LastName>Soltani</LastName>
        <affiliation locale="en_US">Molecular Immunology Research Center, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Samaneh</FirstName>
        <LastName>Zoghi</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Molecular Immunology Research Center, Tehran University of Medical Sciences, Tehran, Iran. AND Medical Genetics Network (MeGeNe), Universal Scientific Education and Research Network (USERN), Vienna, Austria.</affiliation>
      </Author>
      <Author>
        <FirstName>Reza</FirstName>
        <LastName>Shervin Badv</LastName>
        <affiliation locale="en_US">Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mahmoud Reza</FirstName>
        <LastName>Ashrafi</LastName>
        <affiliation locale="en_US">Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Nima</FirstName>
        <LastName>Rezaei</LastName>
        <affiliation locale="en_US">Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran. AND Department of Immunology, School of Medicine, Molecular Immunology Research Center, Tehran University of Medical Sciences, Tehran, Iran. AND Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Sheffield, UK.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Inflammatory elements and genetics have major roles in febrile seizures (FS) pathogenesis. Seventy patients were enrolled and compared with 139 controls. The allele and genotype frequency of the IL-2 gene at -330 and +166 positions and the IFN-&#x3B3; at +874 position were determined. A significant positive association with GG genotype at position -330 in the patient group was found (P=0.003). Further, a positive association was detected in simple and complex FS groups at the same position (P=0.03, P=0.004). IL-2 GT haplotype was significantly more common in the patients compared to controls (P=0.0008). Higher frequency of GT haplotype was detected in simple FS patients in comparison to controls (P=0.0003). Contrary, IL-2 TG haplotype frequency was lower in complex FS group (P=0.005). Overrepresentation of certain alleles, genotypes and haplotypes in IL-2 gene in FS patients could predispose individuals to this disease.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/5713</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/5713/4945</pdf_url>
  </Article>
</Articles>
