Cargando…

Association of Candidate Single Nucleotide Polymorphisms Related to Candidate Genes in Patients With Schizophrenia

INTRODUCTION: Schizophrenia is a chronic heterogenic neurodevelopment disorder. Many genes interfere in the development of SCZ. All four genes, NrCAM, PRODH, ANK3, and ANKK1, which were evaluated in this study, were previously reported to be associated with Schizophrenia. The NrCAM contributes to cr...

Descripción completa

Detalles Bibliográficos
Autores principales: Karimian, Seyedeh Sara, Akbari, Mohammad Taghi, Sadr, Seyed Saeed, Javadi, Gholamreza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Neuroscience Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7878058/
https://www.ncbi.nlm.nih.gov/pubmed/33643553
http://dx.doi.org/10.32598/bcn.9.10.470
_version_ 1783650280589492224
author Karimian, Seyedeh Sara
Akbari, Mohammad Taghi
Sadr, Seyed Saeed
Javadi, Gholamreza
author_facet Karimian, Seyedeh Sara
Akbari, Mohammad Taghi
Sadr, Seyed Saeed
Javadi, Gholamreza
author_sort Karimian, Seyedeh Sara
collection PubMed
description INTRODUCTION: Schizophrenia is a chronic heterogenic neurodevelopment disorder. Many genes interfere in the development of SCZ. All four genes, NrCAM, PRODH, ANK3, and ANKK1, which were evaluated in this study, were previously reported to be associated with Schizophrenia. The NrCAM contributes to creating cognitive deficiencies through the CAM’s signaling pathway. PRODH plays a vital role in creating SCZ negative symptoms through the signaling pathway of glutamatergic and NMDA receptors. ANK3 affects ion channel and molecular adhesion in Ranvier and initial segments of axons, leading to mental retardation, sleep disorder, and SCZ. ANKK1 encodes a protein kinase and was reported to be associated with alcohol addiction, Attention Deficit Hyperactivity Disorder (ADHD), and SCZ. METHODS: The subjects were selected from Schizophrenic patients referring to the Psychiatric Ward of Imam-Hussein Hospital and Schizophrenic Patients Support Institution (AHEBBA). 95 (30 Schizoaffective patients, 57 Paranoid patients, and 8 disorganized) patients were recruited as the subjects in the present case-control association study. 120 healthy subjects were recruited from the Tehran Medical Genetics Laboratory staff and a group of students from the Islamic Azad University of Science and Research in Tehran. The genotypes were determined with molecular genotyping techniques of PCR-RFLP, ARMS-PCR, and Cycle sequencing. Results were analyzed by the Chi-Square test using SPSS V. 24 and R, SNP STATE Package to investigate significant differences between cases and controls. RESULTS: The incidence of schizophrenia was 68% and 32% among men and women, respectively. The evaluation of the allelic association between schizophrenia and all the candidate SNPs showed a significant association between NrCAM’s SNP rs10235968 and SCZ (P=0.001). Haplotype T, T, C in rs10235968, rs6967368, rs3763463, respectively, within the NrCAM gene, showed significant association with schizophrenia disorder (P=0.0001). CONCLUSION: No association was found between other candidate SNPs and SCZ among the subjects.
format Online
Article
Text
id pubmed-7878058
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Iranian Neuroscience Society
record_format MEDLINE/PubMed
spelling pubmed-78780582021-02-27 Association of Candidate Single Nucleotide Polymorphisms Related to Candidate Genes in Patients With Schizophrenia Karimian, Seyedeh Sara Akbari, Mohammad Taghi Sadr, Seyed Saeed Javadi, Gholamreza Basic Clin Neurosci Resaerch Paper INTRODUCTION: Schizophrenia is a chronic heterogenic neurodevelopment disorder. Many genes interfere in the development of SCZ. All four genes, NrCAM, PRODH, ANK3, and ANKK1, which were evaluated in this study, were previously reported to be associated with Schizophrenia. The NrCAM contributes to creating cognitive deficiencies through the CAM’s signaling pathway. PRODH plays a vital role in creating SCZ negative symptoms through the signaling pathway of glutamatergic and NMDA receptors. ANK3 affects ion channel and molecular adhesion in Ranvier and initial segments of axons, leading to mental retardation, sleep disorder, and SCZ. ANKK1 encodes a protein kinase and was reported to be associated with alcohol addiction, Attention Deficit Hyperactivity Disorder (ADHD), and SCZ. METHODS: The subjects were selected from Schizophrenic patients referring to the Psychiatric Ward of Imam-Hussein Hospital and Schizophrenic Patients Support Institution (AHEBBA). 95 (30 Schizoaffective patients, 57 Paranoid patients, and 8 disorganized) patients were recruited as the subjects in the present case-control association study. 120 healthy subjects were recruited from the Tehran Medical Genetics Laboratory staff and a group of students from the Islamic Azad University of Science and Research in Tehran. The genotypes were determined with molecular genotyping techniques of PCR-RFLP, ARMS-PCR, and Cycle sequencing. Results were analyzed by the Chi-Square test using SPSS V. 24 and R, SNP STATE Package to investigate significant differences between cases and controls. RESULTS: The incidence of schizophrenia was 68% and 32% among men and women, respectively. The evaluation of the allelic association between schizophrenia and all the candidate SNPs showed a significant association between NrCAM’s SNP rs10235968 and SCZ (P=0.001). Haplotype T, T, C in rs10235968, rs6967368, rs3763463, respectively, within the NrCAM gene, showed significant association with schizophrenia disorder (P=0.0001). CONCLUSION: No association was found between other candidate SNPs and SCZ among the subjects. Iranian Neuroscience Society 2020 2020-09-01 /pmc/articles/PMC7878058/ /pubmed/33643553 http://dx.doi.org/10.32598/bcn.9.10.470 Text en Copyright© 2020 Iranian Neuroscience Society This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Resaerch Paper
Karimian, Seyedeh Sara
Akbari, Mohammad Taghi
Sadr, Seyed Saeed
Javadi, Gholamreza
Association of Candidate Single Nucleotide Polymorphisms Related to Candidate Genes in Patients With Schizophrenia
title Association of Candidate Single Nucleotide Polymorphisms Related to Candidate Genes in Patients With Schizophrenia
title_full Association of Candidate Single Nucleotide Polymorphisms Related to Candidate Genes in Patients With Schizophrenia
title_fullStr Association of Candidate Single Nucleotide Polymorphisms Related to Candidate Genes in Patients With Schizophrenia
title_full_unstemmed Association of Candidate Single Nucleotide Polymorphisms Related to Candidate Genes in Patients With Schizophrenia
title_short Association of Candidate Single Nucleotide Polymorphisms Related to Candidate Genes in Patients With Schizophrenia
title_sort association of candidate single nucleotide polymorphisms related to candidate genes in patients with schizophrenia
topic Resaerch Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7878058/
https://www.ncbi.nlm.nih.gov/pubmed/33643553
http://dx.doi.org/10.32598/bcn.9.10.470
work_keys_str_mv AT karimianseyedehsara associationofcandidatesinglenucleotidepolymorphismsrelatedtocandidategenesinpatientswithschizophrenia
AT akbarimohammadtaghi associationofcandidatesinglenucleotidepolymorphismsrelatedtocandidategenesinpatientswithschizophrenia
AT sadrseyedsaeed associationofcandidatesinglenucleotidepolymorphismsrelatedtocandidategenesinpatientswithschizophrenia
AT javadigholamreza associationofcandidatesinglenucleotidepolymorphismsrelatedtocandidategenesinpatientswithschizophrenia