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24: ASSOCIATION OF RS3850641 POLYMORPHISM IN OX40 LIGAND GENE AND PREMATURE MYOCARDIAL INFARCTION, SOUTHERN OF IRAN
BACKGROUND AND AIMS: Tumor necrosis factor (TNF) is one of the inflammatory cytokines which has an important role in inflammation and migration of other inflammatory cells to the atherosclerotic plaques. OX40L is a member of the TNF super family receptor protein. OX40 and OX40 ligand are co-stimulat...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759540/ http://dx.doi.org/10.1136/bmjopen-2016-015415.24 |
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author | Rahmanian, Zhila Shojaei, Mohammad Jahromi, Abdolreza Sotoodeh |
author_facet | Rahmanian, Zhila Shojaei, Mohammad Jahromi, Abdolreza Sotoodeh |
author_sort | Rahmanian, Zhila |
collection | PubMed |
description | BACKGROUND AND AIMS: Tumor necrosis factor (TNF) is one of the inflammatory cytokines which has an important role in inflammation and migration of other inflammatory cells to the atherosclerotic plaques. OX40L is a member of the TNF super family receptor protein. OX40 and OX40 ligand are co-stimulators for T-cells and can increase inflammatory response in atherosclerotic plaques. The aim of this study was to determine the association of rs3850641 polymorphism in OX40L gene with premature myocardial infarction. METHODS: This case control study was done on 100 patients with premature acute myocardial infarction (AMI) and a similar number of sex, age and some other cardiovascular risk factor matched healthy people. RESULTS: The OX40L rs3850641 polymorphism was genotyped, using PCR-RFLP method. AA genotype frequency of rs3850641 SNP was higher non-significantly in Premature AMI, compared to healthy subjects (58.80% vs. 57.50%). AG genotype frequency of rs3850641 SNP was lower non-significantly in Premature AMI, compared to healthy subjects (0.0% vs. 1.40%), also GG genotype frequency of rs3850641 SNP was lower non-significantly in Premature AMI, compared to healthy subjects (41.20% vs. 41.10%), (P>0.05). CONCLUSION: The results of this study indicate that the rs3850641 SNP of OX40L gene is not associated with premature AMI in the evaluated population. |
format | Online Article Text |
id | pubmed-5759540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-57595402018-02-12 24: ASSOCIATION OF RS3850641 POLYMORPHISM IN OX40 LIGAND GENE AND PREMATURE MYOCARDIAL INFARCTION, SOUTHERN OF IRAN Rahmanian, Zhila Shojaei, Mohammad Jahromi, Abdolreza Sotoodeh BMJ Open Abstracts from the 5th International Society for Evidence-Based Healthcare Congress, Kish Island, Ira BACKGROUND AND AIMS: Tumor necrosis factor (TNF) is one of the inflammatory cytokines which has an important role in inflammation and migration of other inflammatory cells to the atherosclerotic plaques. OX40L is a member of the TNF super family receptor protein. OX40 and OX40 ligand are co-stimulators for T-cells and can increase inflammatory response in atherosclerotic plaques. The aim of this study was to determine the association of rs3850641 polymorphism in OX40L gene with premature myocardial infarction. METHODS: This case control study was done on 100 patients with premature acute myocardial infarction (AMI) and a similar number of sex, age and some other cardiovascular risk factor matched healthy people. RESULTS: The OX40L rs3850641 polymorphism was genotyped, using PCR-RFLP method. AA genotype frequency of rs3850641 SNP was higher non-significantly in Premature AMI, compared to healthy subjects (58.80% vs. 57.50%). AG genotype frequency of rs3850641 SNP was lower non-significantly in Premature AMI, compared to healthy subjects (0.0% vs. 1.40%), also GG genotype frequency of rs3850641 SNP was lower non-significantly in Premature AMI, compared to healthy subjects (41.20% vs. 41.10%), (P>0.05). CONCLUSION: The results of this study indicate that the rs3850641 SNP of OX40L gene is not associated with premature AMI in the evaluated population. BMJ Publishing Group 2017-02-08 /pmc/articles/PMC5759540/ http://dx.doi.org/10.1136/bmjopen-2016-015415.24 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Abstracts from the 5th International Society for Evidence-Based Healthcare Congress, Kish Island, Ira Rahmanian, Zhila Shojaei, Mohammad Jahromi, Abdolreza Sotoodeh 24: ASSOCIATION OF RS3850641 POLYMORPHISM IN OX40 LIGAND GENE AND PREMATURE MYOCARDIAL INFARCTION, SOUTHERN OF IRAN |
title | 24: ASSOCIATION OF RS3850641 POLYMORPHISM IN OX40 LIGAND GENE AND PREMATURE MYOCARDIAL INFARCTION, SOUTHERN OF IRAN |
title_full | 24: ASSOCIATION OF RS3850641 POLYMORPHISM IN OX40 LIGAND GENE AND PREMATURE MYOCARDIAL INFARCTION, SOUTHERN OF IRAN |
title_fullStr | 24: ASSOCIATION OF RS3850641 POLYMORPHISM IN OX40 LIGAND GENE AND PREMATURE MYOCARDIAL INFARCTION, SOUTHERN OF IRAN |
title_full_unstemmed | 24: ASSOCIATION OF RS3850641 POLYMORPHISM IN OX40 LIGAND GENE AND PREMATURE MYOCARDIAL INFARCTION, SOUTHERN OF IRAN |
title_short | 24: ASSOCIATION OF RS3850641 POLYMORPHISM IN OX40 LIGAND GENE AND PREMATURE MYOCARDIAL INFARCTION, SOUTHERN OF IRAN |
title_sort | 24: association of rs3850641 polymorphism in ox40 ligand gene and premature myocardial infarction, southern of iran |
topic | Abstracts from the 5th International Society for Evidence-Based Healthcare Congress, Kish Island, Ira |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759540/ http://dx.doi.org/10.1136/bmjopen-2016-015415.24 |
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