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LINE-1 Hypomethylation is Associated with the Risk of Coronary Heart Disease in Chinese Population

BACKGROUND: Global methylation level in blood leukocyte DNA has been associated with the risk of coronary heart disease (CHD), with inconsistent results in various populations. Similar data are lacking in Chinese population where different genetic, lifestyle and environmental factors may affect DNA...

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Autores principales: Wei, Li, Liu, Shuchuan, Su, Zhendong, Cheng, Rongchao, Bai, Xiuping, Li, Xueqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Cardiologia 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051451/
https://www.ncbi.nlm.nih.gov/pubmed/24918913
http://dx.doi.org/10.5935/abc.20140054
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author Wei, Li
Liu, Shuchuan
Su, Zhendong
Cheng, Rongchao
Bai, Xiuping
Li, Xueqi
author_facet Wei, Li
Liu, Shuchuan
Su, Zhendong
Cheng, Rongchao
Bai, Xiuping
Li, Xueqi
author_sort Wei, Li
collection PubMed
description BACKGROUND: Global methylation level in blood leukocyte DNA has been associated with the risk of coronary heart disease (CHD), with inconsistent results in various populations. Similar data are lacking in Chinese population where different genetic, lifestyle and environmental factors may affect DNA methylation and its risk relationship with CHD. OBJECTIVES: To examine whether global methylation is associated with the risk of CHD in Chinese population. METHODS: A total of 334 cases with CHD and 788 healthy controls were included. Global methylation in blood leukocyte DNA was estimated by analyzing LINE-1 repeats using bisulfite pyrosequencing. RESULTS: In an initial analysis restricted to control subjects, LINE-1 level reduced significantly with aging, elevated total cholesterol, and diagnosis of diabetes. In the case-control analysis, reduced LINE-1 methylation was associated with increased risk of CHD; analysis by quartile revealed odds ratios (95%CI) of 0.9 (0.6-1.4), 1.9 (1.3-2.9) and 2.3 (1.6-3.5) for the third, second and first (lowest) quartile (P(trend )< 0.001), respectively, compared to the fourth (highest) quartile. Lower (<median) LINE-1 methylation was associated with a 2.2-fold (95%CI = 1.7-3.0) increased risk of CHD. The lower LINE-1-related CHD risk estimates tended to be stronger among subjects with the highest tertile of homocysteine (P(interaction )= 0.042) and those with diagnosis of hypertension (P(interaction )= 0.012). CONCLUSION: LINE-1 hypomethylation is associated with the risk of CHD in Chinese population. Potential CHD risk factors such as older age, elevated total cholesterol, and diagnosis of diabetes may have impact on global DNA methylation, whereby exerting their effect on CHD risk.
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spelling pubmed-40514512014-06-12 LINE-1 Hypomethylation is Associated with the Risk of Coronary Heart Disease in Chinese Population Wei, Li Liu, Shuchuan Su, Zhendong Cheng, Rongchao Bai, Xiuping Li, Xueqi Arq Bras Cardiol Original Articles BACKGROUND: Global methylation level in blood leukocyte DNA has been associated with the risk of coronary heart disease (CHD), with inconsistent results in various populations. Similar data are lacking in Chinese population where different genetic, lifestyle and environmental factors may affect DNA methylation and its risk relationship with CHD. OBJECTIVES: To examine whether global methylation is associated with the risk of CHD in Chinese population. METHODS: A total of 334 cases with CHD and 788 healthy controls were included. Global methylation in blood leukocyte DNA was estimated by analyzing LINE-1 repeats using bisulfite pyrosequencing. RESULTS: In an initial analysis restricted to control subjects, LINE-1 level reduced significantly with aging, elevated total cholesterol, and diagnosis of diabetes. In the case-control analysis, reduced LINE-1 methylation was associated with increased risk of CHD; analysis by quartile revealed odds ratios (95%CI) of 0.9 (0.6-1.4), 1.9 (1.3-2.9) and 2.3 (1.6-3.5) for the third, second and first (lowest) quartile (P(trend )< 0.001), respectively, compared to the fourth (highest) quartile. Lower (<median) LINE-1 methylation was associated with a 2.2-fold (95%CI = 1.7-3.0) increased risk of CHD. The lower LINE-1-related CHD risk estimates tended to be stronger among subjects with the highest tertile of homocysteine (P(interaction )= 0.042) and those with diagnosis of hypertension (P(interaction )= 0.012). CONCLUSION: LINE-1 hypomethylation is associated with the risk of CHD in Chinese population. Potential CHD risk factors such as older age, elevated total cholesterol, and diagnosis of diabetes may have impact on global DNA methylation, whereby exerting their effect on CHD risk. Sociedade Brasileira de Cardiologia 2014-05 /pmc/articles/PMC4051451/ /pubmed/24918913 http://dx.doi.org/10.5935/abc.20140054 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Wei, Li
Liu, Shuchuan
Su, Zhendong
Cheng, Rongchao
Bai, Xiuping
Li, Xueqi
LINE-1 Hypomethylation is Associated with the Risk of Coronary Heart Disease in Chinese Population
title LINE-1 Hypomethylation is Associated with the Risk of Coronary Heart Disease in Chinese Population
title_full LINE-1 Hypomethylation is Associated with the Risk of Coronary Heart Disease in Chinese Population
title_fullStr LINE-1 Hypomethylation is Associated with the Risk of Coronary Heart Disease in Chinese Population
title_full_unstemmed LINE-1 Hypomethylation is Associated with the Risk of Coronary Heart Disease in Chinese Population
title_short LINE-1 Hypomethylation is Associated with the Risk of Coronary Heart Disease in Chinese Population
title_sort line-1 hypomethylation is associated with the risk of coronary heart disease in chinese population
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051451/
https://www.ncbi.nlm.nih.gov/pubmed/24918913
http://dx.doi.org/10.5935/abc.20140054
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