Interactions between<i> CYP11B2</i> Promoter Methylation and Smoking Increase Risk of Essential Hypertension

Gu, Tianlun; Mao, Shuqi; Fan, Rui; Zhong, Fade; Zhu, Fubao; Hao, Lingmei; Zhang, Lina; Yin, Fengying

doi:https://doi.org/10.1155/2016/1454186

BioMed Research International

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Research Article | Open Access

Volume 2016 | Article ID 1454186 | https://doi.org/10.1155/2016/1454186

Interactions between CYP11B2 Promoter Methylation and Smoking Increase Risk of Essential Hypertension

Tianlun Gu,¹Shuqi Mao,¹Rui Fan,²Fade Zhong,³Fubao Zhu,⁴Lingmei Hao,⁵Lina Zhang,¹and Fengying Yin⁶

Academic Editor: Xin-yuan Guan

Received24 May 2016

Revised17 Sept 2016

Accepted09 Oct 2016

Published19 Dec 2016

Abstract

Aldosterone synthase (CYP11B2) is closely linked to essential hypertension (EH). However, it remains unclear whether the methylation of the CYP11B2 promoter is involved in the development of EH in humans. Our study is aimed at evaluating the contribution of CYP11B2 promoter methylation to the risk of EH. Methylation levels were measured using pyrosequencing technology in 192 participants in a hospital-based case-control study. Logistic regression and multiple linear regression analyses were utilized to adjust for confounding factors and the GMDR method was applied to investigate high-order gene-environment interactions. Although no significant result was observed linking the four analyzed CpG sites to EH, GMDR detected significant interactions among CpG1, CpG3, CpG4, and smoking correlated with an increased risk of EH (OR = 4.62, adjusted ). In addition, CpG2 (adjusted ) and CpG3 (adjusted ) methylation was significantly lower in healthy males than in healthy females. Likewise, after adjusting for confounding factors, CpG2 methylation (adjusted ) still showed significant gender-specific differences among the participants of the study. CpG1 () site was significantly positively correlated with age, and CpG3 () and CpG4 () were both inversely linked to smoking. Our findings suggest that gene-environment interactions are associated with the pathogenesis and progression of EH.

1. Introduction

Essential hypertension (EH), a complex chronic noncommunicable disease, is a major risk factor for cardiovascular disease (CVD) and mortality, determined by multiple genetic and environmental factors. Annually, approximately 9.4 million deaths are attributed to high blood pressure as one of three leading risk factors for global disease burden (GDB) [1, 2]. Although the mechanisms underlying the blood pressure changes in EH remain to be fully elucidated, the renin-angiotensin-aldosterone system (RAAS) has been documented to play crucial roles.

Aldosterone synthase (CYP11B2), an important member of RAAS, is a key enzyme for the synthesis of aldosterone and the CYP11B2 gene has been listed as one of the candidate genes of EH. Previous evidence from Stella et al. suggested that aldosterone synthase -344C/T polymorphism was positively correlated with left ventricular (LV) mass and thickness in EH [3, 4]. The CYP11B2 gene -344C/T polymorphism is also associated with atrial fibrillation (AF) [5, 6]. Another recent study also identified the variants of CYP11B2 associated with increased risk of EH [7]. Although the influences of genetic factors on blood pressure (BP) variation in humans are estimated to be responsible for 30% to 50% [8], an alteration of DNA without sequence changes, named epigenetics, likely plays crucial roles as well.

Promoter methylation of genes susceptible to EH has been investigated in numerous recent studies. Hypomethylation of AGTR1b as a result of protein-poor maternal diet in gestating fetuses, which could lead to overexpression of the gene in the adrenal glands, has been implicated in the development of hypertension during adulthood in rats [9, 10]. Similarly, hypomethylation of the AGTR1 promoter was reported to be associated with the risk of EH in humans [11]. Rangel et al. also observed that discrete methylation changes in the ACE promoter had an effect on systolic blood pressure (SBP) and angiotensin I converting enzyme (ACE) activity levels [12]. Based on current evidence, it is clear that aberrant methylation of genes in RAAS is closely related to EH.

As EH is a complex and multifactorial disease, gene-environment interactions contribute significantly to the onset and progression of EH. However, due to the “curse of dimensionality,” structuring models based on traditional statistical methods has already been deemed unfit for investigating potential or undetectable interactions. Recently, a generalized multifactor dimensionality reduction (GMDR) approach emerged as a promising tool and has been used for detecting gene-gene and gene-environment interactions in either dichotomous or continuous phenotypes, as well as permitting adjustment for discrete and quantitative covariates and enhancing prediction accuracy [13, 14]. The GMDR method was successfully employed to deduce the interaction between ADD1 methylation and alcohol consumption leading to increased risk of EH [15].

To date, however, the association between CYP11B2 methylation and EH risk is unclear. Thus, the goal of the current study is to explore whether the aberrant methylation of CYP11B2 is linked to EH risk and further explore the roles of gene-environment interactions in EH risk. In addition, we intend to detect the association among age, gender, clinical variables, and DNA methylation, which are demonstrated in previous studies.

2. Materials and Methods

2.1. Ethics Statement

This was a hospital-based case-control study. The study protocol conformed to the ethical guidelines of the 1975 Declaration of Helsinki and was approved by the Ethics Committee of Ningbo Seventh Hospital. Written informed consent was obtained from all the participating subjects.

2.2. Study Population

A total of 192 individuals, 96 cases with and the other half without EH, were recruited at the Ningbo Seventh Hospital for health examination in Ningbo City, Zhejiang, China. Patients were defined as hypertensive based on systolic blood pressure (SBP) ≥ 140 mmHg or diastolic blood pressure (DBP) ≥ 90 mmHg, in accordance with the 2013 European Society of Hypertension and European Society of Cardiology Guidelines [16]. In addition, all hypertensive participants were incident cases receiving no therapy for hypertension regardless of drug, physical status, and nutrition. Normotensive controls, with SBP < 120 mmHg and DBP < 80 mmHg, had no history of diabetes mellitus (DM), secondary hypertension, myocardial infarction, stroke, renal failure, drug abuse, or other serious diseases and no family history of hypertension in first-degree relatives and were well matched in age (±3 years) and sex within the case group. All the participants, 30 to 75 years old, were sampled from the Han nationality residing in Ningbo for at least three generations. Blood pressure was measured twice at an interval of 10 min in the supine position and the mean value of the two readings was recorded by diverse trained technicians using a calibrated mercury sphygmomanometer with an adult-sized cuff according to standard protocols of the American Heart Association [17, 18]. Following successive 12 h fast overnight, blood samples were drawn from the antecubital vein, using vacutainer tubes containing EDTA, by licensed practical nurses and stored at −80°C for DNA extraction.

2.3. Biochemical Analyses

Routine blood tests including total cholesterol, triglyceride, uric acid, low-density lipoprotein (LDL), high-density lipoprotein (HDL), homocysteine (Hcy), and glucose were measured enzymatically, using an AU2700 automatic analyzer (Olympus, Tokyo, Japan). Genomic DNA was extracted from peripheral blood samples using a Lab-Acid 820 nucleic acid extraction analyzer (Zeesan Biotech, Xiamen, China), and the DNA concentration was detected using a NanoDrop 2000 ultra-micro nucleic acid ultraviolet tester (Thermo Fisher Scientific, Wilmington, DE, USA).

2.4. Pyrosequencing Array

Firstly, we positioned CpG island (CGI) using MethPrimer (http://www.urogene.org/cgi-bin/methprimer/methprimer.cgi) [19]. In addition, for the CpG sites of the promoter region of our interest, PCR primers were designed based on general principles and suggestion of primer design [20] and the scores were automatically outputted by the PyroMark Assay Design v2.0.1.15 (Qiagen). To measure DNA methylation levels, we employed pyrosequencing, a novel widely used sequencing-by-synthesis method, in our study. The explicit operational program was employed and described in our previous research. Briefly, unmethylated cytosine residues of the target sequences of the candidate gene are first converted to thymine, using sodium bisulfite (EpiTect Bisulfite Kit, Qiagen, Hilden, Germany). The converted DNA is then amplified by polymerase chain reaction (PCR) using Mastercycler Nexus Gradient (Eppendorf, Hamburg, Germany), followed by “sequencing by synthesis” of the target (PyroMark Gold Q96, Qiagen) [21, 22]. The PCR reaction mixture consisted of 12 μL ZymoTaq™ Premix (Zymo Research Corporation, Irvine, CA, USA), 8 μL DNase/RNase-free water, 2 μL converted DNA, and 1.5 μL of each of the forward and reverse primers. The target was amplified by the forward primer 5′-GTGGTGGTGGTATATGTTT-3′ and the reverse primer 5′-ATCCCCCAAACTAAAATACA-3′, and the primer 5′-TTAGTTATTTGGGAGG-3′ was used to detect the target sequence. The reaction cycle comprised initial denaturation at 95°C for 10 min, followed by amplification at 95°C for 30 sec, 46.8°C for 40 sec, and 72°C for 50 sec over 45 cycles, followed by final extension at 72°C for 7 min.

2.5. Statistical Analyses

Data analysis was performed on PASW Statistics 18.0 (SPSS, Inc., Somers, NY, USA). Results are presented as the mean ± SD or number (percentages) of patients. Continuous variables such as DNA methylation, age, body mass index (BMI), total cholesterol (TC), triglycerides (TG), glucose, blood uric acid (BUA), high- and low-density lipoprotein, and homocysteine (Hcy) were compared using independent samples -test or nonparametric test. Pearson chi-square or Fisher’s exact test was used to evaluate the correlation between EH and categorical variables such as gender, tobacco usage, and alcohol consumption. Pearson correlation analysis was used to investigate interactions among the four CpG sites in the CYP11B2 promoter. Logistic regression and multiple linear regression were performed with the objective of detecting true association after adjustment for confounders. GMDR was used to investigate high-order interactions among diverse variables.

3. Results

3.1. Baseline Characteristics of the Study Participants

A total of 192 participants (mean age: years; 60.4% women) including 96 patients with EH and 96 gender- and age-matched (±3 years) healthy controls were enrolled, and their baseline characteristics are presented in Table 1. No significant differences in gender and age were detected between EH patients and healthy controls (), demonstrating the well-restricted nature of the study population for gender and age.

CpG island (CGI) was identified in the promoter of the CYP11B2 gene by using MethPrimer (http://www.urogene.org/cgi-bin/methprimer/methprimer.cgi) [19]. Subsequently, a target fragment containing four CpG dinucleotides in the above target island (chr8: 144000685–144001049) was selected (Figure 1). The correlation among these four CpG sites is presented in Figure 1 ().

3.2. Interactions between Promoter Methylation and Environmental Factors to EH

According to our results, EH was not significantly associated with methylation levels of all four CpG sites after adjusting for age, gender, BUA, smoking, drinking, BMI, TG, HDL, LDL, and Hcy. Due to the complex and multifactorial nature of EH, the effect of a single or several sites cannot sufficiently explain the pathogenesis of EH. Subsequently, interactions between methylation of CpG sites and environmental factors including smoking and alcohol use were studied with GMDR. The best models at various orders are summarized in Table 2. The four-factor interaction model of tobacco usage and DNA methylation (CpG1, CpG3, and CpG4) was the best model, along with the best training balanced accuracy (0.68), testing balanced accuracy (0.60), and cross-validation consistency (10/10). The consistency of the model across 10-fold cross-validation training sets is that how many times the same GMDR model is identified in all the possible training sets. Among this set of the best significant models (), we pick the model that has the maximum prediction accuracy with the least error and/or maximum cross-validation consistency. The model’s adjusted value was 0.011 after the sign test, and odds ratio (OR) was 4.62 with 95% confidence interval (1.49, 14.34).

3.3. Analysis of Clinical Variables and EH

Methylation of CpG2 (adjusted ) and CpG3 (adjusted ) was significantly lower in healthy males than in healthy females after adjusting for confounding factors (Table 3 and Figure 2). However, there were no significant differences between EH in males and females for the four CpG sites’ methylation (Table 4). After adjusting for confounding factors, CpG2 methylation (adjusted ) still showed a significant gender-specific difference among all the participants (Table 5). As listed in Table 1, significant differences between essential hypertensive and healthy participants were also detected in ALP (), GGT (), BMI (), TG (), HDL (), and BUA (). Therefore, multiple linear regression was used for testing whether these clinical variables were associated with methylation of the CYP11B2 promoter in different dimensionalities. As a result, in healthy controls, CpG1 (, ) site was significantly positively correlated with age, and CpG3 (, ) and CpG4 (, ) were both inversely linked to smoking (Table 3). However, in EH patients, just CpG1 (, ) site was significantly positively correlated with age (Table 4). And, in the whole study population, CpG1 (, ) site was significant positively correlated with age and CpG4 (, ) site was negatively linked to smoking (Table 5).

4. Discussion

Previous studies demonstrated that the polymorphic variation of CYP11B2, the gene encoding aldosterone synthase, was associated with increased aldosterone metabolite excretion and hypertension [23–27]. In the current study, we hypothesized that aberrant methylation of the CYP11B2 promoter might also account for EH risk. Although no significant link was observed between the four analyzed CpG sites and EH, the interactions between CYP11B2 promoter methylation (CpG1, CpG3, and CpG4) and smoking were significantly correlated with the risk of EH. In addition, we found that methylation of CpG2 and CpG3 was significantly different between males and females in healthy controls. CpG2 methylation exhibited gender-specific differences among all the participants, and CpG1 methylation was significantly positively linked to age, while CpG3 and CpG4 methylation was negatively correlated with smoking. Our results broaden the picture of the pathogenesis of EH.

In general, promoter hypermethylation suppresses transcription, but hypomethylation activates transcription [28]. Therefore, if promoter methylation of the gene encoding key enzymes involved in the pathogenesis of EH was negatively correlated with the incidence of EH, its hypomethylation would increase the prevalence risk of EH. Indeed, promoter hypomethylation augments expression of AGTR1, which increases the risk of EH [11]. One study has demonstrated, based on integrated analysis of genome-wide methylation and gene expression data in the adrenal cortex tissue samples, that the CYP11B2 gene is differentially methylated and expressed through an epigenetic mechanism [29]. In the current study, we did not find any significant results between the four tested CpG methylation instances of CYP11B2 promoter and EH, even though the statistical power of our study was 0.931. Epigenetic changes, however, could interplay with or be mediated through a multitude of environmental and dietary factors. With the GMDR method, we structured gene-environment interaction models and detected a crucially significant four-order synergistic effect among CpG1, CpG3, and CpG4 methylation and smoking (), contributing strongly to the risk of EH. Previous studies consistently reported that some factors had no main effects whereas the interactions played key roles. According to the evidence presented by Taylor et al., two SNPs were detected providing support for powerful genetic interactions with cigarette smoking associated with SBP in African Americans from genome-wide studies, but no main genetic effect linked to SBP was detected with only these two SNPs in the model [30]. Smoking is a major environmental risk factor of EH, and previous studies reported that interactions between environmental factors and epigenetic phenomena may be synergistic [31]. Indeed, the present study found that individuals with hypomethylated CpG3 and CpG4 sites had 4.62-fold increased risk of EH when coupled with smoking, further documenting the interactions between DNA methylation and environmental factors, which could influence the development of EH. Nevertheless, the concrete biological mechanism of the above interactions remains unclear, and further studies are required.

In our research, we found significantly lower CpG2 and CpG3 methylation levels in males compared to females in healthy controls. After adjusting for confounding factors, CpG2 methylation still showed a significant gender-specific difference among the participants. Such sex-related differences are common and widespread in the incidence of CVD [32, 33]. Steroid sex hormones have been postulated as the primary contributor to these sex-specific differences. Estrogen is widely accepted as a positive effector, providing significant protection against the development of CVD, but these benefits fade away following menopause [34], while testosterone is thought to be harmful or detrimental to heart function. Moreover, DNA methylation profiles show that the dynamic regulatory elements are responsive to environmental stimuli, such as tobacco usage, alcohol consumption, sedentariness, high-sodium diet, age, and other silent inimical-to-health factors [35–37], altering the DNA methylation intensities of EH risk genes and causing EH over time. Indeed, our results also revealed that smoking interplayed with DNA methylation. Meanwhile, environmental factors listed above can be hazardous to people’s health leading to the development of chronic diseases. Since lifestyle or behavior factors such as tobacco usage, alcohol consumption, and lack of physical exercise are too inveterately formed to change for people, and, of difference between females and males, our results of sex-related CYP11B2 methylation discrepancy may reveal in advance that these acquired nonhereditary risk factors could influence the genetic variants via diverse enigmatic mechanisms. Earlier studies have also reported age-related changes in DNA methylation [38, 39]. We also found that CpG1 was negatively correlated with age, but the mechanism remains unclear, which requires further study.

In summary, our study detects the interactions between the CYP11B2 promoter methylation (CpG1, CpG3, and CpG4) and smoking, which may increase the risk of EH. Further, age, gender, and smoking are likely to influence CYP11B2 methylation levels. These findings can help us further the understanding of the pathogenesis of EH.

Competing Interests

The authors declared that no competing interests exist.

Authors’ Contributions

Tianlun Gu, Shuqi Mao, and Rui Fan contributed equally to this work.

Acknowledgments

This work was supported by Zhejiang Province Social Development Research Project (2016C33178), K. C. Wong Magna Fund in Ningbo University, Ningbo Social Development Research Project (2014C50051), the Scientific Research Innovation Foundation of Ningbo University (G15070 and G16097), and Ningbo Scientific Innovation Team for Environmental Hazardous Factor Control and Prevention (2016C51001).

References

D. Peiris, S. R. Thompson, A. Beratarrechea et al., “Behaviour change strategies for reducing blood pressure-related disease burden: findings from a global implementation research programme,” Implementation Science, vol. 10, no. 1, p. 158, 2015.
View at: Publisher Site | Google Scholar
S. S. Lim, T. Vos, A. D. Flaxman et al., “A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010,” The Lancet, vol. 380, no. 9859, pp. 2224–2260, 2012.
View at: Google Scholar
M. Cwynar, J. Gąsowski, B. Gryglewska et al., “The relation between ACE D/I and CYP11B2 C-344T polymorphisms and parameters of arterial stiffness in the context of renal sodium handling,” Blood Pressure, vol. 24, no. 5, pp. 306–316, 2015.
View at: Publisher Site | Google Scholar
P. Stella, G. Bigatti, L. Tizzoni et al., “Association between aldosterone synthase (CYP11B2) polymorphism and left ventricular mass in human essential hypertension,” Journal of the American College of Cardiology, vol. 43, no. 2, pp. 265–270, 2004.
View at: Publisher Site | Google Scholar
W.-H. Lu, M. Bayike, J.-W. Liu et al., “Association between aldosterone synthase (CYP11B2) -344C/T polymorphism and atrial fibrillation among Han and Kazak residents of the Xinjiang region,” International Journal of Clinical and Experimental Medicine, vol. 8, no. 4, pp. 5513–5519, 2015.
View at: Google Scholar
Y.-Y. Li, C.-W. Zhou, J. Xu, Y. Qian, and B. Wang, “CYP11B2 T-344C gene polymorphism and atrial fibrillation: a meta-analysis of 2,758 subjects,” PLoS ONE, vol. 7, no. 11, Article ID e50910, 2012.
View at: Publisher Site | Google Scholar
Z. Hlubocká, M. Jáchymová, S. Heller et al., “Association of the -344T/C aldosterone synthase gene variant with essential hypertension,” Physiological Research, vol. 58, no. 6, pp. 785–792, 2009.
View at: Google Scholar
S. Mandai, T. Mori, E. Sohara, T. Rai, and S. Uchida, “Generation of hypertension-associated STK39 polymorphism knockin cell lines with the clustered regularly interspaced short palindromic repeats/Cas9 system,” Hypertension, vol. 66, no. 6, pp. 1199–1206, 2015.
View at: Publisher Site | Google Scholar
I. Bogdarina, A. Haase, S. Langley-Evans, and A. J. L. Clark, “Glucocorticoid effects on the programming of AT1b angiotensin receptor gene methylation and expression in the rat,” PLoS ONE, vol. 5, no. 2, Article ID e9237, 2010.
View at: Publisher Site | Google Scholar
I. G. Bogdarina, P. J. King, and A. J. L. Clark, “Characterization of the angiotensin (AT1b) receptor promoter and its regulation by glucocorticoids,” Journal of Molecular Endocrinology, vol. 43, no. 2, pp. 73–80, 2009.
View at: Publisher Site | Google Scholar
R. Fan, S. Mao, F. Zhong et al., “Association of AGTR1 promoter methylation levels with essential hypertension risk: a matched case-control study,” Cytogenetic and Genome Research, vol. 147, no. 2-3, pp. 95–102, 2015.
View at: Publisher Site | Google Scholar
M. Rangel, J. C. dos Santos, P. H. L. Ortiz et al., “Modification of epigenetic patterns in low birth weight children: importance of hypomethylation of the ACE gene promoter,” PLoS ONE, vol. 9, no. 8, Article ID e106138, 2014.
View at: Publisher Site | Google Scholar
X.-Y. Lou, G.-B. Chen, L. Yan et al., “A generalized combinatorial approach for detecting gene-by-gene and gene-by-environment interactions with application to nicotine dependence,” The American Journal of Human Genetics, vol. 80, no. 6, pp. 1125–1137, 2007.
View at: Publisher Site | Google Scholar
D. Liao, X. Yi, B. Zhang, Z. Qiang, and L. Jing, “Interaction between CYP4F2 rs2108622 and CPY4A11 rs9333025 variants is significantly correlated with susceptibility to ischemic stroke and 20-hydroxyeicosatetraenoic acid level,” Genetic Testing and Molecular Biomarkers, vol. 20, no. 5, pp. 223–228, 2016.
View at: Publisher Site | Google Scholar
L. Han, P. Liu, C. Wang et al., “The interactions between alcohol consumption and DNA methylation of the ADD1 gene promoter modulate essential hypertension susceptibility in a population-based, case-control study,” Hypertension Research, vol. 38, no. 4, pp. 284–290, 2015.
View at: Publisher Site | Google Scholar
S. E. Kjeldsen, T. A. Aksnes, and L. M. Ruilope, “Clinical implications of the 2013 ESH/ESC hypertension guidelines: targets, choice of therapy, and blood pressure monitoring,” Drugs in R&D, vol. 14, no. 2, pp. 31–43, 2014.
View at: Publisher Site | Google Scholar
D. Perloff, C. Grim, J. Flack et al., “Human blood pressure determination by sphygmomanometry,” Circulation, vol. 88, no. 5, part 1, pp. 2460–2470, 1993.
View at: Publisher Site | Google Scholar
G. Parati, G. Stergiou, E. O'Brien et al., “European society of hypertension practice guidelines for ambulatory blood pressure monitoring,” Journal of Hypertension, vol. 32, no. 7, pp. 1359–1366, 2014.
View at: Publisher Site | Google Scholar
L.-C. Li and R. Dahiya, “MethPrimer: designing primers for methylation PCRs,” Bioinformatics, vol. 18, no. 11, pp. 1427–1431, 2002.
View at: Publisher Site | Google Scholar
T. Mikeska, J. Felsberg, C. A. Hewitt, and A. Dobrovic, “Analysing DNA methylation using bisulphite pyrosequencing,” Methods in Molecular Biology, vol. 791, pp. 33–53, 2011.
View at: Publisher Site | Google Scholar
R. Fan, W. J. Wang, Q. L. Zhong et al., “Aberrant methylation of the GCK gene body is associated with the risk of essential hypertension,” Molecular Medicine Reports, vol. 12, no. 2, pp. 2390–2394, 2015.
View at: Google Scholar
L.-N. Zhang, P.-P. Liu, L. Wang et al., “Lower ADD1 gene promoter DNA methylation increases the risk of essential hypertension,” PLoS ONE, vol. 8, no. 5, Article ID e63455, 2013.
View at: Publisher Site | Google Scholar
J. M. C. Connell, R. Fraser, S. M. MacKenzie et al., “The impact of polymorphisms in the gene encoding aldosterone synthase (CYP11B2) on steroid synthesis and blood pressure regulation,” Molecular and Cellular Endocrinology, vol. 217, no. 1-2, pp. 243–247, 2004.
View at: Publisher Site | Google Scholar
B. Chen, S. Nie, S. Luo, W. Zhang, and C. Xiao, “Association of the human CYP11B2 gene and essential hypertension in southwest Han Chinese population: a haplotype-based case-control study,” Clinical and Experimental Hypertension, vol. 33, no. 2, pp. 106–112, 2011.
View at: Publisher Site | Google Scholar
E. Brand, N. Chatelain, P. Mulatero et al., “Structural analysis and evaluation of the aldosterone synthase gene in hypertension,” Hypertension, vol. 32, no. 2, pp. 198–204, 1998.
View at: Publisher Site | Google Scholar
Y. Song, K. Miyaki, J. Araki et al., “Influence of CYP11B2 gene polymorphism on the prevalence of hypertension and the blood pressure in Japanese men: interaction with dietary salt intake,” Journal of Nutrigenetics and Nutrigenomics, vol. 1, no. 5, pp. 252–258, 2008.
View at: Publisher Site | Google Scholar
N. Iwai, K. Kajimoto, H. Tomoike, and N. Takashima, “Polymorphism of CYP11B2 determines salt sensitivity in Japanese,” Hypertension, vol. 49, no. 4, pp. 825–831, 2007.
View at: Publisher Site | Google Scholar
A. M. Deaton and A. Bird, “CpG islands and the regulation of transcription,” Genes and Development, vol. 25, no. 10, pp. 1010–1022, 2011.
View at: Publisher Site | Google Scholar
B. Howard, Y. Wang, P. Xekouki et al., “Integrated analysis of genome-wide methylation and gene expression shows epigenetic regulation of CYP11B2 in aldosteronomas,” Journal of Clinical Endocrinology and Metabolism, vol. 99, no. 3, pp. E536–E543, 2014.
View at: Publisher Site | Google Scholar
J. Y. Taylor, K. Schwander, S. L. R. Kardia et al., “A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction,” Scientific Reports, vol. 6, Article ID 18812, 10 pages, 2016.
View at: Publisher Site | Google Scholar
J. Simino, D. C. Rao, and B. I. Freedman, “Novel findings and future directions on the genetics of hypertension,” Current Opinion in Nephrology and Hypertension, vol. 21, no. 5, pp. 500–507, 2012.
View at: Publisher Site | Google Scholar
L. Pilote, K. Dasgupta, V. Guru et al., “A comprehensive view of sex-specific issues related to cardiovascular disease,” Canadian Medical Association Journal, vol. 176, no. 6, pp. S1–S44, 2007.
View at: Google Scholar
S. Intapad, N. B. Ojeda, J. H. Dasinger, and B. T. Alexander, “Sex differences in the developmental origins of cardiovascular disease,” Physiology, vol. 29, no. 2, pp. 122–132, 2014.
View at: Publisher Site | Google Scholar
L. Pedersen, D. Frestad, M. M. Michelsen et al., “Risk factors for myocardial infarction in women and men: a review of the current literature,” Current Pharmaceutical Design, vol. 22, no. 25, pp. 3835–3852, 2016.
View at: Publisher Site | Google Scholar
J. Odeberg, M. Freitag, H. Forssell et al., “The influence of smoking and impaired glucose homoeostasis on the outcome in patients presenting with an acute coronary syndrome: a cross-sectional study,” BMJ Open, vol. 4, no. 7, Article ID e005077, 2014.
View at: Publisher Site | Google Scholar
A. M. Kanaya, D. Grady, and E. Barrett-Connor, “Explaining the sex difference in coronary heart disease mortality among patients with type 2 diabetes mellitus: a meta-analysis,” Archives of Internal Medicine, vol. 162, no. 15, pp. 1737–1745, 2002.
View at: Publisher Site | Google Scholar
D. Aronson, E. J. Rayfield, and J. H. Chesebro, “Mechanisms determining course and outcome of diabetic patients who have had acute myocardial infarction,” Annals of Internal Medicine, vol. 126, no. 4, pp. 296–306, 1997.
View at: Publisher Site | Google Scholar
M. R. Penner, R. R. Parrish, L. T. Hoang, T. L. Roth, F. D. Lubin, and C. A. Barnes, “Age-related changes in Egr1 transcription and DNA methylation within the hippocampus,” Hippocampus, vol. 26, no. 8, pp. 1008–1020, 2016.
View at: Google Scholar
D. Punzo, F. Errico, L. Cristino et al., “Age-related changes in d-aspartate oxidase promoter methylation control extracellular d-aspartate levels and prevent precocious cell death during brain aging,” The Journal of Neuroscience, vol. 36, no. 10, pp. 3064–3078, 2016.
View at: Publisher Site | Google Scholar

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Copyright © 2016 Tianlun Gu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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