No association between the SNP rs1625579 in miR-137 gene and schizophrenia in Iranian population

Background: Schizophrenia is a common and severe neuropsychiatric disorder with symptoms such as hallucination, delusion and mental disease. Among candidate genes for schizophrenia, miR-137 gene has been recently suggested to contribute to schizophrenia by genome-wide association study (GWAS) and a...

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Main Authors: Azadeh Abtahi, Nader Mansour Samaei, Naghmeh Gholipour, Noorodin Moradi
Format: Article
Language:English
Published: SpringerOpen 2018-07-01
Series:Egyptian Journal of Medical Human Genetics
Online Access:http://www.sciencedirect.com/science/article/pii/S1110863017301222
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spelling doaj-6fcd2f701c0a4121939cd9b8366c1fcd2020-11-25T01:17:51ZengSpringerOpenEgyptian Journal of Medical Human Genetics1110-86302018-07-01193247251No association between the SNP rs1625579 in miR-137 gene and schizophrenia in Iranian populationAzadeh Abtahi0Nader Mansour Samaei1Naghmeh Gholipour2Noorodin Moradi3Sana University of Sari, Sari, Iran; Corresponding author.Department of Medical Genetics, Golestan University of Medical Sciences, Gorgan, IranNational Institute of Genetic Engineering and Biotechnology, Tehran, IranNational Institute of Genetic Engineering and Biotechnology, Tehran, IranBackground: Schizophrenia is a common and severe neuropsychiatric disorder with symptoms such as hallucination, delusion and mental disease. Among candidate genes for schizophrenia, miR-137 gene has been recently suggested to contribute to schizophrenia by genome-wide association study (GWAS) and a single nucleotide polymorphism (SNP) rs1625579 (G>T) as a presumed risk allele within an intron of miR-137 gene has been contributed by schizophrenia. Since mir-137 is a considerable gene in the performance of neural systems, the present study dealt with the association between SNP rs1625579 in miR-137 gene and schizophrenia in Iranian patients. Aim of study: This study aimed to evaluate the association between SNP rs1625579 in miR-137 gene and schizophrenia in Iranian patients. Methods: Hoping to identify a single-nucleotide polymorphism as a possible locus for schizophrenia, we carried out this case-control study on 80 blood samples collected from individuals suffering from schizophrenia and 48 healthy controls. DNA was extracted from the samples, and the frequency of the polymorphisms was analyzed using ARMS-PCR method. Finally, the products were detected on 1.5% agarose gel electrophoresis. Results: The analysis on the data showed that 43.75% of the patients and 37.5% of the controls were mutant homozygous and 56.25% of the patients and 62.5% of controls were heterozygous. In addition, 0.0% of the patients and 0.0% of the controls were normal homozygous. Both the genotype (p = .48 > .05) and allele (p = .5 > .05) distribution of the rs1625579 SNP has no significant difference between patients and controls. Conclusion: There was no significant relationship between rs1625579 and the incidence of schizophrenia. To the best of our knowledge, this is first study in Iran that assesses the frequency of the polymorphism among Iranian patients. However, further studies with more samples are necessary. Keywords: MIR137 gene, Rs1625579, Schizophrenia, Polymorphism, Iranhttp://www.sciencedirect.com/science/article/pii/S1110863017301222
collection DOAJ
language English
format Article
sources DOAJ
author Azadeh Abtahi
Nader Mansour Samaei
Naghmeh Gholipour
Noorodin Moradi
spellingShingle Azadeh Abtahi
Nader Mansour Samaei
Naghmeh Gholipour
Noorodin Moradi
No association between the SNP rs1625579 in miR-137 gene and schizophrenia in Iranian population
Egyptian Journal of Medical Human Genetics
author_facet Azadeh Abtahi
Nader Mansour Samaei
Naghmeh Gholipour
Noorodin Moradi
author_sort Azadeh Abtahi
title No association between the SNP rs1625579 in miR-137 gene and schizophrenia in Iranian population
title_short No association between the SNP rs1625579 in miR-137 gene and schizophrenia in Iranian population
title_full No association between the SNP rs1625579 in miR-137 gene and schizophrenia in Iranian population
title_fullStr No association between the SNP rs1625579 in miR-137 gene and schizophrenia in Iranian population
title_full_unstemmed No association between the SNP rs1625579 in miR-137 gene and schizophrenia in Iranian population
title_sort no association between the snp rs1625579 in mir-137 gene and schizophrenia in iranian population
publisher SpringerOpen
series Egyptian Journal of Medical Human Genetics
issn 1110-8630
publishDate 2018-07-01
description Background: Schizophrenia is a common and severe neuropsychiatric disorder with symptoms such as hallucination, delusion and mental disease. Among candidate genes for schizophrenia, miR-137 gene has been recently suggested to contribute to schizophrenia by genome-wide association study (GWAS) and a single nucleotide polymorphism (SNP) rs1625579 (G>T) as a presumed risk allele within an intron of miR-137 gene has been contributed by schizophrenia. Since mir-137 is a considerable gene in the performance of neural systems, the present study dealt with the association between SNP rs1625579 in miR-137 gene and schizophrenia in Iranian patients. Aim of study: This study aimed to evaluate the association between SNP rs1625579 in miR-137 gene and schizophrenia in Iranian patients. Methods: Hoping to identify a single-nucleotide polymorphism as a possible locus for schizophrenia, we carried out this case-control study on 80 blood samples collected from individuals suffering from schizophrenia and 48 healthy controls. DNA was extracted from the samples, and the frequency of the polymorphisms was analyzed using ARMS-PCR method. Finally, the products were detected on 1.5% agarose gel electrophoresis. Results: The analysis on the data showed that 43.75% of the patients and 37.5% of the controls were mutant homozygous and 56.25% of the patients and 62.5% of controls were heterozygous. In addition, 0.0% of the patients and 0.0% of the controls were normal homozygous. Both the genotype (p = .48 > .05) and allele (p = .5 > .05) distribution of the rs1625579 SNP has no significant difference between patients and controls. Conclusion: There was no significant relationship between rs1625579 and the incidence of schizophrenia. To the best of our knowledge, this is first study in Iran that assesses the frequency of the polymorphism among Iranian patients. However, further studies with more samples are necessary. Keywords: MIR137 gene, Rs1625579, Schizophrenia, Polymorphism, Iran
url http://www.sciencedirect.com/science/article/pii/S1110863017301222
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