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血管紧张素II 1型受体(AGTR1)基因的低甲基化与环境因素共同增加原发性高血压风险。

Hypomethylation of the Angiotensin II Type I Receptor (AGTR1) Gene Along with Environmental Factors Increases the Risk for Essential Hypertension.

作者信息

Lin Jiabing, Lin Shaowei, Wu Yihai, Wang Xiaoxia, Wu Siying, Li Huangyuan

机构信息

Department of Epidemiology and Health Statistics, Fujian Provincial Key Laboratory of Environment Factors and Cancer, School of Public Health, Fujian Medical University, Fuzhou, China.

出版信息

Cardiology. 2017;137(2):126-135. doi: 10.1159/000458520. Epub 2017 Apr 4.

Abstract

OBJECTIVES

The present study aimed to evaluate the hypertension status of community residents, analyze environmental and epigenetic factors, and propose prevention measures for hypertension.

METHODS

In our study, different methylation levels were distinguished utilizing melting temperature (Tm) values in both the case and the control group. Multiple logistic regression analysis was used to estimate the risk of having essential hypertension (EH) between hypertensive and nonhypertensive participants. A receiver-operating characteristic curve was used to analyze Tm cutoff levels of methylation.

RESULTS

The average DNA Tm was 71.784 with a standard deviation of 0.210. The Tm value of community residents (Fujian, China) was inversely correlated with systolic and diastolic blood pressure. Student t test analysis showed a clear separation in Tm expression levels between the hypertensive and the control group (p < 0.05). The Tm value was lower in the hypertension group than in the normotensive group. Multivariate regression analysis showed that high levels of DNA methylation were a protective factor in hypertension with adjustment of demographic and environmental factors, whereas when the Tm value increased by 0.1 units, the risk of hypertension was reduced by 0.652 times. Patients that smoked and consumed an irregular diet demonstrated a lower degree of methylation in the presence of hypertension.

CONCLUSIONS

DNA methylation affects the risk for the development of hypertension; therefore, epigenetic markers could be used to measure hypertension levels to help elucidate the pathogenesis of EH.

摘要

目的

本研究旨在评估社区居民的高血压状况,分析环境和表观遗传因素,并提出高血压的预防措施。

方法

在我们的研究中,利用病例组和对照组的解链温度(Tm)值区分不同的甲基化水平。采用多元逻辑回归分析来估计高血压参与者和非高血压参与者患原发性高血压(EH)的风险。使用受试者工作特征曲线分析甲基化的Tm临界水平。

结果

平均DNA Tm为71.784,标准差为0.210。社区居民(中国福建)的Tm值与收缩压和舒张压呈负相关。学生t检验分析显示高血压组和对照组之间的Tm表达水平有明显差异(p<0.05)。高血压组的Tm值低于正常血压组。多变量回归分析表明,在调整人口统计学和环境因素后,高水平的DNA甲基化是高血压中的一个保护因素,而当Tm值增加0.1个单位时,高血压风险降低0.652倍。吸烟和饮食不规律的患者在患高血压时甲基化程度较低。

结论

DNA甲基化影响高血压发生的风险;因此,表观遗传标记可用于测量高血压水平,以帮助阐明EH的发病机制。

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