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Effects of CDKN2B‐AS1 polymorphisms on the susceptibility to coronary heart disease

BACKGROUND: Coronary heart disease (CHD) is one of the most severe cardiovascular diseases. Cyclin‐dependent kinase inhibitor 2B antisense RNA 1 (CDKN2B‐AS1) is a significant susceptibility locus for cardiovascular disease by regulating inflammation response and cell cycle. The aim of this study was...

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Autores principales: Huang, Kang, Zhong, Jianghua, Li, Qiang, Zhang, Wei, Chen, Zibin, Zhou, Yilei, Wu, Miao, Zhong, Zanrui, Lu, Shijuan, Zhang, Shufang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825846/
https://www.ncbi.nlm.nih.gov/pubmed/31496134
http://dx.doi.org/10.1002/mgg3.955
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author Huang, Kang
Zhong, Jianghua
Li, Qiang
Zhang, Wei
Chen, Zibin
Zhou, Yilei
Wu, Miao
Zhong, Zanrui
Lu, Shijuan
Zhang, Shufang
author_facet Huang, Kang
Zhong, Jianghua
Li, Qiang
Zhang, Wei
Chen, Zibin
Zhou, Yilei
Wu, Miao
Zhong, Zanrui
Lu, Shijuan
Zhang, Shufang
author_sort Huang, Kang
collection PubMed
description BACKGROUND: Coronary heart disease (CHD) is one of the most severe cardiovascular diseases. Cyclin‐dependent kinase inhibitor 2B antisense RNA 1 (CDKN2B‐AS1) is a significant susceptibility locus for cardiovascular disease by regulating inflammation response and cell cycle. The aim of this study was to assess whether CDKN2B‐AS1 polymorphisms are associated with CHD risk in the Chinese Han population. METHODS: A total of 501 CHD patients and 496 healthy controls were recruited from Central South University Xiangya School of Medicine Affiliated Haikou Hospital, five CDKN2B‐AS1 polymorphisms (rs10115049, rs75227345, rs2383205, rs10738606, and rs1333049) were analyzed by the Agena MassARRAY platform. The association of CDKN2B‐AS1 polymorphisms and CHD risk was determined by odd ratios (OR) and 95% confidence intervals (CI) using logistic regression. RESULTS: CDKN2B‐AS1 rs10738606 was significantly associated with CHD under codominant (p = .03), dominant (p = .019), recessive (p = .010), additive (p = .003), and allele (p = .003) models. Gender‐based subgroup tests showed that four polymorphisms (rs75227345, rs2383205, rs10738606 and rs1333049) were associated with CHD in males (p < .05). And age‐based subgroup tests indicated that rs2383205 and rs10738606 were associated with CHD among individuals, respectively (p < .05). For CHD patients, rs1333049 decreased the risk of diabetes under heterozygote (p = .014) and dominant (p = .024) models. CONCLUSIONS: In conclusion, CDKN2B‐AS1 polymorphisms were associated with CHD risk in the combined or subgroup tests, suggesting an important role of CDKN2B‐AS1 in CHD susceptibility.
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spelling pubmed-68258462019-11-07 Effects of CDKN2B‐AS1 polymorphisms on the susceptibility to coronary heart disease Huang, Kang Zhong, Jianghua Li, Qiang Zhang, Wei Chen, Zibin Zhou, Yilei Wu, Miao Zhong, Zanrui Lu, Shijuan Zhang, Shufang Mol Genet Genomic Med Original Articles BACKGROUND: Coronary heart disease (CHD) is one of the most severe cardiovascular diseases. Cyclin‐dependent kinase inhibitor 2B antisense RNA 1 (CDKN2B‐AS1) is a significant susceptibility locus for cardiovascular disease by regulating inflammation response and cell cycle. The aim of this study was to assess whether CDKN2B‐AS1 polymorphisms are associated with CHD risk in the Chinese Han population. METHODS: A total of 501 CHD patients and 496 healthy controls were recruited from Central South University Xiangya School of Medicine Affiliated Haikou Hospital, five CDKN2B‐AS1 polymorphisms (rs10115049, rs75227345, rs2383205, rs10738606, and rs1333049) were analyzed by the Agena MassARRAY platform. The association of CDKN2B‐AS1 polymorphisms and CHD risk was determined by odd ratios (OR) and 95% confidence intervals (CI) using logistic regression. RESULTS: CDKN2B‐AS1 rs10738606 was significantly associated with CHD under codominant (p = .03), dominant (p = .019), recessive (p = .010), additive (p = .003), and allele (p = .003) models. Gender‐based subgroup tests showed that four polymorphisms (rs75227345, rs2383205, rs10738606 and rs1333049) were associated with CHD in males (p < .05). And age‐based subgroup tests indicated that rs2383205 and rs10738606 were associated with CHD among individuals, respectively (p < .05). For CHD patients, rs1333049 decreased the risk of diabetes under heterozygote (p = .014) and dominant (p = .024) models. CONCLUSIONS: In conclusion, CDKN2B‐AS1 polymorphisms were associated with CHD risk in the combined or subgroup tests, suggesting an important role of CDKN2B‐AS1 in CHD susceptibility. John Wiley and Sons Inc. 2019-09-08 /pmc/articles/PMC6825846/ /pubmed/31496134 http://dx.doi.org/10.1002/mgg3.955 Text en © 2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Huang, Kang
Zhong, Jianghua
Li, Qiang
Zhang, Wei
Chen, Zibin
Zhou, Yilei
Wu, Miao
Zhong, Zanrui
Lu, Shijuan
Zhang, Shufang
Effects of CDKN2B‐AS1 polymorphisms on the susceptibility to coronary heart disease
title Effects of CDKN2B‐AS1 polymorphisms on the susceptibility to coronary heart disease
title_full Effects of CDKN2B‐AS1 polymorphisms on the susceptibility to coronary heart disease
title_fullStr Effects of CDKN2B‐AS1 polymorphisms on the susceptibility to coronary heart disease
title_full_unstemmed Effects of CDKN2B‐AS1 polymorphisms on the susceptibility to coronary heart disease
title_short Effects of CDKN2B‐AS1 polymorphisms on the susceptibility to coronary heart disease
title_sort effects of cdkn2b‐as1 polymorphisms on the susceptibility to coronary heart disease
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825846/
https://www.ncbi.nlm.nih.gov/pubmed/31496134
http://dx.doi.org/10.1002/mgg3.955
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