• Title of article

    Association between Neuregulin-1 Gene Variant ‎‎(rs2439272) and Schizophrenia and its Negative ‎Symptoms in an Iranian Population

  • Author/Authors

    Yoosefee، Sadegh نويسنده Department of Neuroscience, School of Advanced Technologies in Medicine, Iran University of Medical Sciences Yoosefee, Sadegh , Shahsavand Ananloo، Esmaeil نويسنده MD, Psychiatric Research Center, Roozbeh Psychiatric Hospital, TUMS, Tehran , , Joghataei ، Mohammad-Taghi نويسنده Neuroscience Department, School of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran , , karimipour، Morteza نويسنده Molecular Medicine Group, Biotechnology research Centre, Pasteur Institute , , Hadjighassem، Mahmoudreza نويسنده Department of Neuroscience, School of Advanced Medical Technologies, Tehran University of Medical Sciences, Tehran, IR Iran , , Mohaghghegh، Hoorie نويسنده Department of Neuroscience and addiction studies, School of Advanced Technologies in Medicine, Tehran ‎University of Medical ‎Sciences (TUMS), Tehran, Iran. Mohaghghegh, Hoorie , Tehrani-Doost، Mehdi نويسنده , , Rahimi، Amir-Abbas نويسنده Molecular Medicine Group, Pasteur Institute of Iran. Rahimi, Amir-Abbas , Mostafavi Abdolmaleky، Hamid نويسنده , , Hatami، Maryam نويسنده ,

  • Issue Information
    فصلنامه با شماره پیاپی 0 سال 2016
  • Pages
    7
  • From page
    147
  • To page
    153
  • Abstract

    Objective: Although the etiology of schizophrenia is unknown, it has a significant genetic component. ‎A number of studies have indicated that neuregulin-1 (NRG1) gene may play a role in the ‎pathogenesis of schizophrenia. In this study, we examined whether the rs2439272 of NRG1 ‎is associated with schizophrenia and its negative symptoms in an Iranian population.‎

    Method: Rs2439272 was genotyped in 469 participants including 276 unrelated patients with schizophrenia and 193 healthy controls. The association of genetic risk with PANSS, and negative ‎symptoms was examined in the total, male and female samples. COCAPHASE and ‎CLUMP22 programs were used to compare the allele and genotype frequencies, and ‎general linear regression was used to analyze the quantitative dependent variables by the ‎selected variant.‎

    Results: In this study, it was revealed that the G allele of rs2439272 might be an allele with the ‎increased risk of developing schizophrenia, especially in the male participants. In addition, ‎significant differences were found between the G allele and GG genotype frequencies and ‎PANSS, and negative symptoms in the total and male participants.‎

    Conclusion: Our results supported the association between rs2439272 in NRG1 gene and risk of ‎schizophrenia and its negative symptoms in an Iranian population.
  • Journal title
    Iranian Journal of Psychiatry
  • Serial Year
    2016
  • Journal title
    Iranian Journal of Psychiatry
  • Record number

    2395470