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Association between CYP3A4 gene rs4646437 polymorphism and the risk of hypertension in Chinese population: a case–control study

Using a case–control design, we assessed the association between single nucleotide polymorphisms of CYP3A4 gene rs4646437 polymorphism and the risk of hypertension in Chinese population. We recruited 450 hypertension patients from The First Clinical College, Henan University of Chinese Medicine betw...

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Autores principales: Wang, Juan, Ji, Hongliang, Jia, Helei, Guan, Dongsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470406/
https://www.ncbi.nlm.nih.gov/pubmed/30910847
http://dx.doi.org/10.1042/BSR20190296
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author Wang, Juan
Ji, Hongliang
Jia, Helei
Guan, Dongsheng
author_facet Wang, Juan
Ji, Hongliang
Jia, Helei
Guan, Dongsheng
author_sort Wang, Juan
collection PubMed
description Using a case–control design, we assessed the association between single nucleotide polymorphisms of CYP3A4 gene rs4646437 polymorphism and the risk of hypertension in Chinese population. We recruited 450 hypertension patients from The First Clinical College, Henan University of Chinese Medicine between June 2017 and May 2018. There was a significant difference in genotype distribution between case group and control group (χ(2)=18.169, P=0.000). The minor A allele was significantly higher in the case group than that in the control group (31.0 vs 24.8%, P=0.000, odds ratio [OR]=1.36, 95% confidence interval [95% CI]: 1.12–1.66). Significant differences were also observed in other gene models: the GA/AA genotype did not increase the risk of hypertension compared with GG genotype (OR=1.16, 95% CI: 0.90–1.49, P=0.259). Compared with GG/GA genotype, the AA genotype also increased the risk of hypertension (OR=2.34, 95% CI: 1.56–3.50, P=0.000). For additive model, the AA genotype was significantly associated with GG genotype (OR=2.25, 95% CI: 1.49–3.42, P=0.000). The same results were found for AA vs GA (OR=2.50, 95% CI: 1.60–3.89, P=0.000). For the allele genotype, the A allele frequency was significantly higher in the case group than that in the control group (31.0 vs 24.8%, P=0.002). The A allele of CYP3A4 rs4646437 was associated with an increased risk for hypertension (OR=1.36, 95% CI: 1.12–1.66, P=0.002). Our results revealed a possible genetic association between CYP3A4 gene rs4646437 and hypertension, and the AA genotype of rs4646437 increased the risk of hypertension in Chinese Han population, and this effect could be confirmed by multivariable analyses.
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spelling pubmed-64704062019-04-26 Association between CYP3A4 gene rs4646437 polymorphism and the risk of hypertension in Chinese population: a case–control study Wang, Juan Ji, Hongliang Jia, Helei Guan, Dongsheng Biosci Rep Research Articles Using a case–control design, we assessed the association between single nucleotide polymorphisms of CYP3A4 gene rs4646437 polymorphism and the risk of hypertension in Chinese population. We recruited 450 hypertension patients from The First Clinical College, Henan University of Chinese Medicine between June 2017 and May 2018. There was a significant difference in genotype distribution between case group and control group (χ(2)=18.169, P=0.000). The minor A allele was significantly higher in the case group than that in the control group (31.0 vs 24.8%, P=0.000, odds ratio [OR]=1.36, 95% confidence interval [95% CI]: 1.12–1.66). Significant differences were also observed in other gene models: the GA/AA genotype did not increase the risk of hypertension compared with GG genotype (OR=1.16, 95% CI: 0.90–1.49, P=0.259). Compared with GG/GA genotype, the AA genotype also increased the risk of hypertension (OR=2.34, 95% CI: 1.56–3.50, P=0.000). For additive model, the AA genotype was significantly associated with GG genotype (OR=2.25, 95% CI: 1.49–3.42, P=0.000). The same results were found for AA vs GA (OR=2.50, 95% CI: 1.60–3.89, P=0.000). For the allele genotype, the A allele frequency was significantly higher in the case group than that in the control group (31.0 vs 24.8%, P=0.002). The A allele of CYP3A4 rs4646437 was associated with an increased risk for hypertension (OR=1.36, 95% CI: 1.12–1.66, P=0.002). Our results revealed a possible genetic association between CYP3A4 gene rs4646437 and hypertension, and the AA genotype of rs4646437 increased the risk of hypertension in Chinese Han population, and this effect could be confirmed by multivariable analyses. Portland Press Ltd. 2019-04-17 /pmc/articles/PMC6470406/ /pubmed/30910847 http://dx.doi.org/10.1042/BSR20190296 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Wang, Juan
Ji, Hongliang
Jia, Helei
Guan, Dongsheng
Association between CYP3A4 gene rs4646437 polymorphism and the risk of hypertension in Chinese population: a case–control study
title Association between CYP3A4 gene rs4646437 polymorphism and the risk of hypertension in Chinese population: a case–control study
title_full Association between CYP3A4 gene rs4646437 polymorphism and the risk of hypertension in Chinese population: a case–control study
title_fullStr Association between CYP3A4 gene rs4646437 polymorphism and the risk of hypertension in Chinese population: a case–control study
title_full_unstemmed Association between CYP3A4 gene rs4646437 polymorphism and the risk of hypertension in Chinese population: a case–control study
title_short Association between CYP3A4 gene rs4646437 polymorphism and the risk of hypertension in Chinese population: a case–control study
title_sort association between cyp3a4 gene rs4646437 polymorphism and the risk of hypertension in chinese population: a case–control study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470406/
https://www.ncbi.nlm.nih.gov/pubmed/30910847
http://dx.doi.org/10.1042/BSR20190296
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