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Single-nucleotide Polymorphism of CTLA-4 (rs5742909) in Correlation with Schizophrenia Risk Factor
BACKGROUND: Cytotoxic T protein lymphocyte antigen-4 (CTLA-4) plays a key role in regulating the T-cell system, where occurrence of disturbances in the system seen by imbalances in Th1 and Th2 levels is believed to be one of the etiologies of schizophrenia. Single-nucleotide polymorphisms (SNPs) at...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7020830/ https://www.ncbi.nlm.nih.gov/pubmed/32148371 http://dx.doi.org/10.4103/jpbs.JPBS_215_19 |
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author | Sumirtanurdin, Riyadi Laksono, James P. Dania, Haafizah Ramadhani, Fitri N. Perwitasari, Dyah A. Abdulah, Rizky Barliana, Melisa I. |
author_facet | Sumirtanurdin, Riyadi Laksono, James P. Dania, Haafizah Ramadhani, Fitri N. Perwitasari, Dyah A. Abdulah, Rizky Barliana, Melisa I. |
author_sort | Sumirtanurdin, Riyadi |
collection | PubMed |
description | BACKGROUND: Cytotoxic T protein lymphocyte antigen-4 (CTLA-4) plays a key role in regulating the T-cell system, where occurrence of disturbances in the system seen by imbalances in Th1 and Th2 levels is believed to be one of the etiologies of schizophrenia. Single-nucleotide polymorphisms (SNPs) at rs5742909 in the CTLA-4 gene (C→T) might affect the expression level of CTLA-4 protein. AIMS AND OBJECTIVES: The aim of this study was to determine the genotype distribution of the CTLA-4 gene (rs5742909) in patients with schizophrenia at Rumah Sakit Jiwa Prof. Dr. Soerojo Magelang and identify the correlation of these genetic polymorphisms as the risk factors of schizophrenia. MATERIALS AND METHODS: This research was conducted through the stage of submitting ethical approval, primer design, chromosomal DNA isolation, optimization of polymerase chain reaction conditions, and data analysis. RESULTS: Based on the results of the study, the CC genotype was shown in 36 patients (78.26%), TT genotype in 10 patients (21.73%), and no TT genotypes. However, statistical analysis using Fisher’s exact and binary logistic regression statistical test showed no significant relationship between genetic polymorphism of the CTLA-4 rs5742909 against risk factors for schizophrenia (P = 0.05; α = 5%). CONCLUSION: SNP at rs5742909, C-to-T-allele transition, was not significant associated with the risk of schizophrenia. |
format | Online Article Text |
id | pubmed-7020830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-70208302020-03-06 Single-nucleotide Polymorphism of CTLA-4 (rs5742909) in Correlation with Schizophrenia Risk Factor Sumirtanurdin, Riyadi Laksono, James P. Dania, Haafizah Ramadhani, Fitri N. Perwitasari, Dyah A. Abdulah, Rizky Barliana, Melisa I. J Pharm Bioallied Sci Original Article BACKGROUND: Cytotoxic T protein lymphocyte antigen-4 (CTLA-4) plays a key role in regulating the T-cell system, where occurrence of disturbances in the system seen by imbalances in Th1 and Th2 levels is believed to be one of the etiologies of schizophrenia. Single-nucleotide polymorphisms (SNPs) at rs5742909 in the CTLA-4 gene (C→T) might affect the expression level of CTLA-4 protein. AIMS AND OBJECTIVES: The aim of this study was to determine the genotype distribution of the CTLA-4 gene (rs5742909) in patients with schizophrenia at Rumah Sakit Jiwa Prof. Dr. Soerojo Magelang and identify the correlation of these genetic polymorphisms as the risk factors of schizophrenia. MATERIALS AND METHODS: This research was conducted through the stage of submitting ethical approval, primer design, chromosomal DNA isolation, optimization of polymerase chain reaction conditions, and data analysis. RESULTS: Based on the results of the study, the CC genotype was shown in 36 patients (78.26%), TT genotype in 10 patients (21.73%), and no TT genotypes. However, statistical analysis using Fisher’s exact and binary logistic regression statistical test showed no significant relationship between genetic polymorphism of the CTLA-4 rs5742909 against risk factors for schizophrenia (P = 0.05; α = 5%). CONCLUSION: SNP at rs5742909, C-to-T-allele transition, was not significant associated with the risk of schizophrenia. Wolters Kluwer - Medknow 2019-12 2019-12-30 /pmc/articles/PMC7020830/ /pubmed/32148371 http://dx.doi.org/10.4103/jpbs.JPBS_215_19 Text en Copyright: © 2019 Journal of Pharmacy and Bioallied Sciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Sumirtanurdin, Riyadi Laksono, James P. Dania, Haafizah Ramadhani, Fitri N. Perwitasari, Dyah A. Abdulah, Rizky Barliana, Melisa I. Single-nucleotide Polymorphism of CTLA-4 (rs5742909) in Correlation with Schizophrenia Risk Factor |
title | Single-nucleotide Polymorphism of CTLA-4 (rs5742909) in Correlation with Schizophrenia Risk Factor |
title_full | Single-nucleotide Polymorphism of CTLA-4 (rs5742909) in Correlation with Schizophrenia Risk Factor |
title_fullStr | Single-nucleotide Polymorphism of CTLA-4 (rs5742909) in Correlation with Schizophrenia Risk Factor |
title_full_unstemmed | Single-nucleotide Polymorphism of CTLA-4 (rs5742909) in Correlation with Schizophrenia Risk Factor |
title_short | Single-nucleotide Polymorphism of CTLA-4 (rs5742909) in Correlation with Schizophrenia Risk Factor |
title_sort | single-nucleotide polymorphism of ctla-4 (rs5742909) in correlation with schizophrenia risk factor |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7020830/ https://www.ncbi.nlm.nih.gov/pubmed/32148371 http://dx.doi.org/10.4103/jpbs.JPBS_215_19 |
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