﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Tabriz University of Medical Sciences</PublisherName>
      <JournalTitle>BioImpacts</JournalTitle>
      <Issn>2228-5652</Issn>
      <Volume>7</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2017</Year>
        <Month>09</Month>
        <DAY>11</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>The study of association between reduced folate carrier 1 (RFC1) polymorphism and non-syndromic cleft lip/palate in Iranian population</ArticleTitle>
    <FirstPage>263</FirstPage>
    <LastPage>268</LastPage>
    <ELocationID EIdType="doi">10.15171/bi.2017.31</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Behnoosh</FirstName>
        <LastName>Soghani</LastName>
      </Author>
      <Author>
        <FirstName>Asghar</FirstName>
        <LastName>Ebadifar</LastName>
      </Author>
      <Author>
        <FirstName>Hamid Reza</FirstName>
        <LastName>Khorram Khorshid</LastName>
      </Author>
      <Author>
        <FirstName>Koorosh</FirstName>
        <LastName>Kamali</LastName>
      </Author>
      <Author>
        <FirstName>Roya</FirstName>
        <LastName>Hamedi</LastName>
      </Author>
      <Author>
        <FirstName>Fatemeh</FirstName>
        <LastName>Aghakhani Moghadam</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.15171/bi.2017.31</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>09</Month>
        <Day>23</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>11</Month>
        <Day>23</Day>
      </PubDate>
    </History>
    <Abstract>Introduction: Cleft lip/palate is one of the most common congenital defects and is supposed to have multifactorial etiology, including a complex interaction between genetics and environment. Reduced folate carrier 1 (RFC1) gene takes part in folate transportation within the cells. In this study, the association of A80G polymorphism in the RFC1 gene with the non-syndromic cleft lip/palate (nsCL/P) was investigated in Iranian infants for the first time.  Methods: In this case-control survey, 122 Iranian infants with nsCL/P and 164 healthy infants were investigated for RFC1 polymorphism by PCR and RFLP methods. The results were statistically compared with control group, odds ratios with 95% CI were estimated by univariate and multivariate logistic regression model and a P &lt;0.05 was considered statistically significant.  Results: The RFC1 G allele was significantly higher (P=0.001; OR=7, 95% CI: 4.7-10.2) in the cases (60.3%) compared with the controls (17.9%). Not only the RFC1 AG genotype was significantly higher (P&lt;0.001; OR=44, 95% CI: 14.6-133) in cases (67.8%) than the controls (27.4%), but also GG genotype (P&lt;0.001; OR=85, 95% CI: 20.5-352) was much higher in cases (26.4%) than the controls (4.3%).  Conclusion: Our study indicated that the RFC1 (A80G) polymorphism was associated with the nsCL/P in Iranian population. Moreover, 80GG homozygosity was significant in the cases. The presence of G allele can be considered as a risk factor for the nsCL/P. Infants with the GG and AG genotypes were more prone to cleft lip/palate as compared to the AA ones. This finding emphasizes the role of RFC1 gene and the intracellular levels of folate.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Cleft lip/palate</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Polymorphism</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">RFC1 gene</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>