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血管紧张素原基因M235T变异与原发性高血压的关联

[Association of angiotensinogen gene M235T variant with essential hypertension].

作者信息

Cai Si-yu, Yu Feng, Shi Yu-ping

机构信息

The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310009, China.

出版信息

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2004 Mar;33(2):151-4. doi: 10.3785/j.issn.1008-9292.2004.02.014.

DOI:10.3785/j.issn.1008-9292.2004.02.014
PMID:15067738
Abstract

OBJECTIVE

To investigate the association of the AGT gene M235T variant with essential hypertension in Han population of Zhejiang Province.

METHODS

The study included 230 subjects: 116 hypertensive patients and 114 normotensive controls. Polymerase chain reaction (PCR) combined with restrictive fragment length polymorphism (RFLP) was used to detect the M235T variant of angiotensinogen (AGT) gene. Blood pressure, body height and weight, fasting blood glucose and serum lipid were measured in all subjects.

RESULTS

(1)The systolic blood pressure and diastolic blood pressure of hypertensive group were significantly higher than those of control group, while no significant difference was observed with regard to age, gender, body mass index, blood glucose, or lipid profile. (2)The genotype distribution of AGT gene in both groups was in agreement with Hardy-Weinberg equilibrium. (3)The genotype distribution of the M235T variant differed significantly in hypertensives and controls (chi(2)=6.966,P<0.05). The frequencies of genotype TT and T235 allele in hypertensives were higher than those in controls (TT genotype: 0.47 compared with 0.33, chi(2)=5.36,P<0.05; T235 allele: 0.71 compared with 0.60, chi(2)=6.179, P<0.05).

CONCLUSION

The molecular variant M235T of the AGT gene is significantly associated with essential hypertension in this population. The genotype TT or allele T235 might be a genetic risk factor for hypertension.

摘要

目的

研究血管紧张素原(AGT)基因M235T变异与浙江省汉族人群原发性高血压的相关性。

方法

本研究纳入230名受试者,其中116例高血压患者和114例血压正常对照者。采用聚合酶链反应(PCR)结合限制性片段长度多态性(RFLP)方法检测血管紧张素原(AGT)基因的M235T变异。测量所有受试者的血压、身高、体重、空腹血糖和血脂。

结果

(1)高血压组的收缩压和舒张压显著高于对照组,而在年龄、性别、体重指数、血糖或血脂方面未观察到显著差异。(2)两组AGT基因的基因型分布均符合Hardy-Weinberg平衡。(3)高血压患者和对照组中M235T变异的基因型分布有显著差异(χ2=6.966,P<0.05)。高血压患者中TT基因型和T235等位基因的频率高于对照组(TT基因型:0.47比0.33,χ2=5.36,P<0.05;T235等位基因:0.71比0.60,χ2=6.179,P<0.05)。

结论

AGT基因的M235T分子变异与该人群的原发性高血压显著相关。TT基因型或T235等位基因可能是高血压的遗传危险因素。

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[Association of angiotensinogen gene M235T variant with essential hypertension].血管紧张素原基因M235T变异与原发性高血压的关联
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