Long non-coding RNA H19 and MALAT1 gene variants in patients with ischemic stroke in a northern Chinese Han population

Abstract Objectives Long non-coding RNAs (lncRNAs) have been identified as key regulators in the development of atherosclerosis, which is a major cause of ischemic stroke. However, to date, there are no reports on the association between lncRNA gene variation and the risk of ischemic stroke. Therefo...

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Main Authors: Ruixia Zhu, Xu Liu, Zhiyi He
Format: Article
Language:English
Published: BMC 2018-10-01
Series:Molecular Brain
Subjects:
H19
Online Access:http://link.springer.com/article/10.1186/s13041-018-0402-7
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spelling doaj-e36a551aaa81436290872a484785361b2020-11-25T01:25:34ZengBMCMolecular Brain1756-66062018-10-011111710.1186/s13041-018-0402-7Long non-coding RNA H19 and MALAT1 gene variants in patients with ischemic stroke in a northern Chinese Han populationRuixia Zhu0Xu Liu1Zhiyi He2Department of Neurology, The First Affiliated Hospital of China Medical UniversityDepartment of Neurology, The First Affiliated Hospital of China Medical UniversityDepartment of Neurology, The First Affiliated Hospital of China Medical UniversityAbstract Objectives Long non-coding RNAs (lncRNAs) have been identified as key regulators in the development of atherosclerosis, which is a major cause of ischemic stroke. However, to date, there are no reports on the association between lncRNA gene variation and the risk of ischemic stroke. Therefore, we assessed the association between H19 and MALAT1 gene polymorphisms and susceptibility to ischemic stroke in a northern Chinese Han population. Methods In our study, we genotyped four genetic variations in lncRNA-H19 and -MALAT1 (rs217727, rs2251375, rs619586, and rs3200401) in a case–control study of 567 ischemic stroke patients and 552 control subjects. Results We found that the TT genotype of the rs217727 polymorphism within H19 was significantly associated with increased risk of ischemic stroke in our northern Chinese Han population (odds ration (OR) = 1.519, 95% confidence interval (CI) = 1.072–2.152, p = 0.018). Stratified analysis based on stroke subtype revealed that the increased risk was more evident in small vessel ischemic stroke (OR = 1.941, 95% CI = 1.260–2.992, p = 0.02). Individuals with the TT genotype had a 1.941 times higher risk of small vessel ischemic stroke when compared with the subjects of CC + CT. These correlations remained after adjusting for confounding risk factors of stroke (OR = 1.913, 95% CI = 1.221–2.998, p = 0.005). However, there was no significant association between H19 rs2251375 or MALAT1 rs3200401 and ischemic stroke in either total population analysis or subgroup analysis. Conclusion In conclusion, our findings suggest that the H19 rs217727 gene polymorphism contributes to small vessel ischemic stroke susceptibility in the Chinese Han population and may serve as a potential indicator for ischemic stroke susceptibility.http://link.springer.com/article/10.1186/s13041-018-0402-7Ischemic strokeGene variantsH19MALAT1
collection DOAJ
language English
format Article
sources DOAJ
author Ruixia Zhu
Xu Liu
Zhiyi He
spellingShingle Ruixia Zhu
Xu Liu
Zhiyi He
Long non-coding RNA H19 and MALAT1 gene variants in patients with ischemic stroke in a northern Chinese Han population
Molecular Brain
Ischemic stroke
Gene variants
H19
MALAT1
author_facet Ruixia Zhu
Xu Liu
Zhiyi He
author_sort Ruixia Zhu
title Long non-coding RNA H19 and MALAT1 gene variants in patients with ischemic stroke in a northern Chinese Han population
title_short Long non-coding RNA H19 and MALAT1 gene variants in patients with ischemic stroke in a northern Chinese Han population
title_full Long non-coding RNA H19 and MALAT1 gene variants in patients with ischemic stroke in a northern Chinese Han population
title_fullStr Long non-coding RNA H19 and MALAT1 gene variants in patients with ischemic stroke in a northern Chinese Han population
title_full_unstemmed Long non-coding RNA H19 and MALAT1 gene variants in patients with ischemic stroke in a northern Chinese Han population
title_sort long non-coding rna h19 and malat1 gene variants in patients with ischemic stroke in a northern chinese han population
publisher BMC
series Molecular Brain
issn 1756-6606
publishDate 2018-10-01
description Abstract Objectives Long non-coding RNAs (lncRNAs) have been identified as key regulators in the development of atherosclerosis, which is a major cause of ischemic stroke. However, to date, there are no reports on the association between lncRNA gene variation and the risk of ischemic stroke. Therefore, we assessed the association between H19 and MALAT1 gene polymorphisms and susceptibility to ischemic stroke in a northern Chinese Han population. Methods In our study, we genotyped four genetic variations in lncRNA-H19 and -MALAT1 (rs217727, rs2251375, rs619586, and rs3200401) in a case–control study of 567 ischemic stroke patients and 552 control subjects. Results We found that the TT genotype of the rs217727 polymorphism within H19 was significantly associated with increased risk of ischemic stroke in our northern Chinese Han population (odds ration (OR) = 1.519, 95% confidence interval (CI) = 1.072–2.152, p = 0.018). Stratified analysis based on stroke subtype revealed that the increased risk was more evident in small vessel ischemic stroke (OR = 1.941, 95% CI = 1.260–2.992, p = 0.02). Individuals with the TT genotype had a 1.941 times higher risk of small vessel ischemic stroke when compared with the subjects of CC + CT. These correlations remained after adjusting for confounding risk factors of stroke (OR = 1.913, 95% CI = 1.221–2.998, p = 0.005). However, there was no significant association between H19 rs2251375 or MALAT1 rs3200401 and ischemic stroke in either total population analysis or subgroup analysis. Conclusion In conclusion, our findings suggest that the H19 rs217727 gene polymorphism contributes to small vessel ischemic stroke susceptibility in the Chinese Han population and may serve as a potential indicator for ischemic stroke susceptibility.
topic Ischemic stroke
Gene variants
H19
MALAT1
url http://link.springer.com/article/10.1186/s13041-018-0402-7
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AT xuliu longnoncodingrnah19andmalat1genevariantsinpatientswithischemicstrokeinanorthernchinesehanpopulation
AT zhiyihe longnoncodingrnah19andmalat1genevariantsinpatientswithischemicstrokeinanorthernchinesehanpopulation
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