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首页> 外文期刊>Journal of hypertension >Gene polymorphisms of the renin-angiotensin system in relation to hypertension and parental history of myocardial infarction and stroke: the PEGASE study. Projet d'Etude des Genes de l'Hypertension Arterielle Severe a moderee Essentielle.
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Gene polymorphisms of the renin-angiotensin system in relation to hypertension and parental history of myocardial infarction and stroke: the PEGASE study. Projet d'Etude des Genes de l'Hypertension Arterielle Severe a moderee Essentielle.

机译:肾素-血管紧张素系统的基因多态性与高血压和父母的心肌梗塞和中风史有关:PEGASE研究。高血压小动脉练习曲轻度的Essentielle。

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OBJECTIVE: To investigate a possible involvement of polymorphisms of the renin-angiotensin system in predisposition to moderate and severe hypertension and their relationship to parental histories of myocardial infarction and stroke. METHODS: Hypertensive cases (453 men, 326 women) were patients followed up by general practitioners for established hypertension. Inclusion criteria were an age of onset of hypertension < or = 60 years and a diastolic blood pressure > or = 105 mmHg without antihypertensive medication or > or = 100 mmHg under treatment. Normotensive controls were selected from population-based samples (362 men) and during a preventative medicine visit (170 women). Polymorphisms of the angiotensinogen gene (AGT M235T and T174M), the angiotensin I converting enzyme gene (ACE I/D), and the angiotensin II type 1 receptor gene (AGT1R A1166C) were investigated. RESULTS: The AGTT235 allele prevalence was higher among male hypertensive cases than it was among controls (0.46 versus 0.40, P = 0.01) and a similar trend was observed with female cases whose hypertension had been diagnosed before they were aged 45 years (0.44 versus 0.38, P = 0.20). The AGT1R C1166 allele prevalence was higher among female hypertensives than it was among controls (0.30 versus 0.23, P = 0.03) but no such difference was observed for men. The AGT T174M and ACE I/D polymorphisms were not associated with hypertension. Hypertensive patients reporting a parental history of myocardial infarction before age 60 years had a higher prevalence of the ACE D allele than did those without such a parental history (0.68 versus 0.56, P = 0.01). The ACE D allele prevalence was also greater among patients reporting a parental history of stroke incidence before age 65 years (0.66 versus 0.57, P = 0.05). CONCLUSIONS: These results support the hypothesis that the AGT gene plays a role in predisposition to hypertension and that the ACE gene plays a role in predisposition to acute ischemic events.
机译:目的:探讨肾素-血管紧张素系统多态性与中,重度高血压易感性及其与父母心肌梗塞和中风病史的关系。方法:高血压病例(男453例,女326例)是由全科医生对确诊的高血压进行随访的患者。入选标准为高血压发作年龄<或= 60岁,舒张压> 105毫米汞柱,而未接受降压药物治疗或≥100毫米汞柱。从基于人群的样本(362名男性)和预防医学访问期间(170名女性)中选择血压正常对照。研究了血管紧张素原基因(AGT M235T和T174M),血管紧张素I转化酶基因(ACE I / D)和血管紧张素II 1型受体基因(AGT1R A1166C)的多态性。结果:男性高血压病例的AGTT235等位基因患病率高于对照组(0.46比0.40,P = 0.01),女性在45岁之前被确诊为高血压的病例也观察到类似趋势(0.44比0.38) ,P = 0.20)。女性高血压患者的AGT1R C1166等位基因患病率高于对照组(0.30对0.23,P = 0.03),但男性没有这种差异。 AGT T174M和ACE I / D多态性与高血压无关。报告了60岁之前有父母心肌梗死病史的高血压患者比无父母史的高血压患者ACE D等位基因患病率更高(0.68对0.56,P = 0.01)。报告父母年龄在65岁之前的卒中发生史的患者中ACE D等位基因患病率也更高(0.66对0.57,P = 0.05)。结论:这些结果支持以下假设:AGT基因在高血压的易感性中起作用,而ACE基因在急性缺血性事件的易感性中起作用。

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