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Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population
BACKGROUND: Stroke is an extremely complicated disease caused by multiple factors. Epidemiological studies have shown that genetic factors contribute to the pathogenesis of stroke. There is still little research on the effect of ApoB gene on stroke in Chinese Han population. The purpose of our resea...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788636/ https://www.ncbi.nlm.nih.gov/pubmed/29416768 http://dx.doi.org/10.18632/oncotarget.23369 |
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author | Zhou, Feng Guo, Tie Zhou, Lv Zhou, Yanhui Yu, Dan |
author_facet | Zhou, Feng Guo, Tie Zhou, Lv Zhou, Yanhui Yu, Dan |
author_sort | Zhou, Feng |
collection | PubMed |
description | BACKGROUND: Stroke is an extremely complicated disease caused by multiple factors. Epidemiological studies have shown that genetic factors contribute to the pathogenesis of stroke. There is still little research on the effect of ApoB gene on stroke in Chinese Han population. The purpose of our research was to explore the effect of ApoB gene polymorphism on the genetic susceptibility to Ischemic Stroke in Chinese Han male population. MATERIALS AND METHODS: 7 polymorphisms in ApoB gene were selected and genotyped using Sequenom MassARRAY in 325 ischemic stroke male patients and 399 healthy male controls in Chinese Han population. The association between ApoB gene and genetic susceptibility to Ischemic Stroke was performed by the χ(2) test, genetic model analysis and haplotype analysis. RESULTS: In the allele model, ApoB rs1042034 “T” allele and rs673548 “G” allele increased the risk of the Ischemic Stroke (rs1042034: OR=1.29, 95%CI: 1.02-1.63, p=0.030; rs673548: OR=1.28, 95%CI: 1.02-1.62, p=0.034). Logistic regression analysis found that ApoB rs1042034 and rs673548 increased the risk of Ischemic Stroke in the log-additive model, the odds of having Ischemic Stroke would be 1.28-fold and 1.27-fold with the variant allele, respectively. We also found that the risk of individuals carrying the ApoB rs693 “AA-AG” genotype had Ischemic Stroke risk of 1.52-fold of carrying “GG” genotype in the dominant model. The haplotype analysis shown that “TAG” haplotype raised the risk of Ischemic Stroke (OR=1.52, 95%CI: 1.02-2.27, p=0.0042). CONCLUSION: The polymorphisms of the ApoB gene may affect Ischemic Stroke occurrence. |
format | Online Article Text |
id | pubmed-5788636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57886362018-02-07 Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population Zhou, Feng Guo, Tie Zhou, Lv Zhou, Yanhui Yu, Dan Oncotarget Research Paper BACKGROUND: Stroke is an extremely complicated disease caused by multiple factors. Epidemiological studies have shown that genetic factors contribute to the pathogenesis of stroke. There is still little research on the effect of ApoB gene on stroke in Chinese Han population. The purpose of our research was to explore the effect of ApoB gene polymorphism on the genetic susceptibility to Ischemic Stroke in Chinese Han male population. MATERIALS AND METHODS: 7 polymorphisms in ApoB gene were selected and genotyped using Sequenom MassARRAY in 325 ischemic stroke male patients and 399 healthy male controls in Chinese Han population. The association between ApoB gene and genetic susceptibility to Ischemic Stroke was performed by the χ(2) test, genetic model analysis and haplotype analysis. RESULTS: In the allele model, ApoB rs1042034 “T” allele and rs673548 “G” allele increased the risk of the Ischemic Stroke (rs1042034: OR=1.29, 95%CI: 1.02-1.63, p=0.030; rs673548: OR=1.28, 95%CI: 1.02-1.62, p=0.034). Logistic regression analysis found that ApoB rs1042034 and rs673548 increased the risk of Ischemic Stroke in the log-additive model, the odds of having Ischemic Stroke would be 1.28-fold and 1.27-fold with the variant allele, respectively. We also found that the risk of individuals carrying the ApoB rs693 “AA-AG” genotype had Ischemic Stroke risk of 1.52-fold of carrying “GG” genotype in the dominant model. The haplotype analysis shown that “TAG” haplotype raised the risk of Ischemic Stroke (OR=1.52, 95%CI: 1.02-2.27, p=0.0042). CONCLUSION: The polymorphisms of the ApoB gene may affect Ischemic Stroke occurrence. Impact Journals LLC 2017-12-18 /pmc/articles/PMC5788636/ /pubmed/29416768 http://dx.doi.org/10.18632/oncotarget.23369 Text en Copyright: © 2018 Zhou et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Zhou, Feng Guo, Tie Zhou, Lv Zhou, Yanhui Yu, Dan Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population |
title | Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population |
title_full | Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population |
title_fullStr | Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population |
title_full_unstemmed | Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population |
title_short | Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population |
title_sort | variants in the apob gene was associated with ischemic stroke susceptibility in chinese han male population |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788636/ https://www.ncbi.nlm.nih.gov/pubmed/29416768 http://dx.doi.org/10.18632/oncotarget.23369 |
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