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Iranian Journal of Psychiatry، جلد ۱۱، شماره ۳، صفحات ۱۴۷-۱۵۳

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عنوان انگلیسی Association between Neuregulin-1 Gene Variant ‎‎(rs2439272) and Schizophrenia and its Negative ‎Symptoms in an Iranian Population
چکیده انگلیسی مقاله 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.
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نویسندگان مقاله | Sadegh Yoosefee
Neuroscience and Neurology Research Center, Qom University of Medical Sciences, Qom, ‎Iran. AND Department of Neuroscience, School of Advanced Technologies in Medicine, Iran ‎University of Medical Sciences ‎‎(IUMS), Tehran, Iran‎.
 AND Health and Religion Research Center, Qom University of Medical Sciences, Qom, Iran.


| Esmaeil Shahsavand Ananloo
Department of Adult Psychiatry, Roozbeh Hospital, School of Medicine, Tehran University of ‎Medical Sciences (TUMS), ‎Tehran, Iran.
 ‎AND Department of Genomic Psychiatry and Behavioral Genomics (DGPBG), Roozbeh ‎Psychiatry Hospital, School of ‎Medicine, Tehran University of Medical Sciences (TUMS), ‎Tehran, Iran.


| Mohammad-Taghi Joghataei
Department of Neuroscience, School of Advanced Technologies in Medicine, Iran ‎University of Medical Sciences ‎‎(IUMS), Tehran, Iran‎.


| Morteza Karimipour
Molecular Medicine Group, Pasteur Institute of Iran.


| Mahmoudreza Hadjighassem
Department of Neuroscience and addiction studies, School of Advanced Technologies in Medicine, Tehran ‎University of 
 Medical ‎Sciences (TUMS), Tehran, Iran.


| Hoorie Mohaghghegh
Department of Neuroscience and addiction studies, School of Advanced Technologies in Medicine, Tehran ‎University of 
 Medical ‎Sciences (TUMS), Tehran, Iran.


| Mehdi Tehrani-Doost
Department of Child and Adolescent Psychiatry, Roozbeh Hospital, School of Medicine, ‎Tehran University of Medical Sciences (TUMS), Tehran, Iran.


| Amir-Abbas Rahimi
Molecular Medicine Group, Pasteur Institute of Iran.


| Hamid Mostafavi Abdolmaleky
Department of Genetics & Genomics, Boston University School of Medicine, Boston, MA, ‎United States.


| Maryam Hatami
Department of Adult Psychiatry, Roozbeh Hospital, School of Medicine, Tehran University of ‎Medical Sciences (TUMS), ‎Tehran, Iran



نشانی اینترنتی http://ijps.tums.ac.ir/index.php/ijps/article/view/778
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