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CBS promoter hypermethylation increases the risk of hypertension and stroke

OBJECTIVES: Cystathionine β-synthase is a major enzyme in the metabolism of plasma homocysteine. Hyperhomocysteinemia is positively associated with hypertension and stroke. The present study was performed to examine the possible effects of Cystathionine β-synthase promoter methylation on the develop...

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Autores principales: Wang, Changyi, Xu, Guodong, Wen, Qi, Peng, Xiaolin, Chen, Hongen, Zhang, Jingwen, Xu, Shan, Zhang, Chunhui, Zhang, Min, Ma, Jianping, Hui, Zhaohui, Wu, Guifu, Ma, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculdade de Medicina / USP 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438132/
https://www.ncbi.nlm.nih.gov/pubmed/30916171
http://dx.doi.org/10.6061/clinics/2019/e630
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author Wang, Changyi
Xu, Guodong
Wen, Qi
Peng, Xiaolin
Chen, Hongen
Zhang, Jingwen
Xu, Shan
Zhang, Chunhui
Zhang, Min
Ma, Jianping
Hui, Zhaohui
Wu, Guifu
Ma, Min
author_facet Wang, Changyi
Xu, Guodong
Wen, Qi
Peng, Xiaolin
Chen, Hongen
Zhang, Jingwen
Xu, Shan
Zhang, Chunhui
Zhang, Min
Ma, Jianping
Hui, Zhaohui
Wu, Guifu
Ma, Min
author_sort Wang, Changyi
collection PubMed
description OBJECTIVES: Cystathionine β-synthase is a major enzyme in the metabolism of plasma homocysteine. Hyperhomocysteinemia is positively associated with hypertension and stroke. The present study was performed to examine the possible effects of Cystathionine β-synthase promoter methylation on the development of hypertension and stroke. METHODS: Using quantitative methylation-specific PCR, we determined the Cystathionine β-synthase methylation levels in 218 healthy individuals and 132 and 243 age- and gender-matched stroke and hypertensive patients, respectively. The relative changes in Cystathionine β-synthase promoter methylation were analyzed using the 2(–)ΔΔ(Ct) method. The percent of the methylated reference of Cystathionine β-synthase was used to represent the Cystathionine β-synthase promoter methylation levels. RESULTS: In this study, the Cystathionine β-synthase promoter methylation levels of hypertensive and stroke participants were both higher than that of the healthy individuals (median percentages of the methylated reference were 50.61%, 38.05% and 30.53%, respectively, all p<0.001). Multivariable analysis showed that Cystathionine β-synthase promoter hypermethylation increased the risk of hypertension [odds ratio, OR (95% confidence interval, CI)=1.035 (1.025–1.045)] and stroke [OR (95% CI)=1.015 (1.003–1.028)]. The area under the curve of Cystathionine β-synthase promoter methylation was 0.844 (95% CI: 0.796–0.892) in male patients with hypertension and 0.722 (95% CI: 0.653–0.799) in male patients with stroke. CONCLUSION: Cystathionine β-synthase promoter hypermethylation increases the risk of hypertension and stroke, especially in male patients.
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spelling pubmed-64381322019-04-01 CBS promoter hypermethylation increases the risk of hypertension and stroke Wang, Changyi Xu, Guodong Wen, Qi Peng, Xiaolin Chen, Hongen Zhang, Jingwen Xu, Shan Zhang, Chunhui Zhang, Min Ma, Jianping Hui, Zhaohui Wu, Guifu Ma, Min Clinics (Sao Paulo) Original Article OBJECTIVES: Cystathionine β-synthase is a major enzyme in the metabolism of plasma homocysteine. Hyperhomocysteinemia is positively associated with hypertension and stroke. The present study was performed to examine the possible effects of Cystathionine β-synthase promoter methylation on the development of hypertension and stroke. METHODS: Using quantitative methylation-specific PCR, we determined the Cystathionine β-synthase methylation levels in 218 healthy individuals and 132 and 243 age- and gender-matched stroke and hypertensive patients, respectively. The relative changes in Cystathionine β-synthase promoter methylation were analyzed using the 2(–)ΔΔ(Ct) method. The percent of the methylated reference of Cystathionine β-synthase was used to represent the Cystathionine β-synthase promoter methylation levels. RESULTS: In this study, the Cystathionine β-synthase promoter methylation levels of hypertensive and stroke participants were both higher than that of the healthy individuals (median percentages of the methylated reference were 50.61%, 38.05% and 30.53%, respectively, all p<0.001). Multivariable analysis showed that Cystathionine β-synthase promoter hypermethylation increased the risk of hypertension [odds ratio, OR (95% confidence interval, CI)=1.035 (1.025–1.045)] and stroke [OR (95% CI)=1.015 (1.003–1.028)]. The area under the curve of Cystathionine β-synthase promoter methylation was 0.844 (95% CI: 0.796–0.892) in male patients with hypertension and 0.722 (95% CI: 0.653–0.799) in male patients with stroke. CONCLUSION: Cystathionine β-synthase promoter hypermethylation increases the risk of hypertension and stroke, especially in male patients. Faculdade de Medicina / USP 2019-03-14 2019 /pmc/articles/PMC6438132/ /pubmed/30916171 http://dx.doi.org/10.6061/clinics/2019/e630 Text en Copyright © 2019 CLINICS https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Wang, Changyi
Xu, Guodong
Wen, Qi
Peng, Xiaolin
Chen, Hongen
Zhang, Jingwen
Xu, Shan
Zhang, Chunhui
Zhang, Min
Ma, Jianping
Hui, Zhaohui
Wu, Guifu
Ma, Min
CBS promoter hypermethylation increases the risk of hypertension and stroke
title CBS promoter hypermethylation increases the risk of hypertension and stroke
title_full CBS promoter hypermethylation increases the risk of hypertension and stroke
title_fullStr CBS promoter hypermethylation increases the risk of hypertension and stroke
title_full_unstemmed CBS promoter hypermethylation increases the risk of hypertension and stroke
title_short CBS promoter hypermethylation increases the risk of hypertension and stroke
title_sort cbs promoter hypermethylation increases the risk of hypertension and stroke
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438132/
https://www.ncbi.nlm.nih.gov/pubmed/30916171
http://dx.doi.org/10.6061/clinics/2019/e630
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