Suppr超能文献

波兰人群原发性高血压中血管紧张素转换酶和血管紧张素II 1型受体基因的多态性

Polymorphisms of angiotensin-converting enzyme and angiotensin II receptor type 1 genes in essential hypertension in a Polish population.

作者信息

Dzida G, Sobstyl J, Puzniak A, Golon P, Mosiewicz J, Hanzlik J

机构信息

1st Department of Internal Medicine, Medical University, Lublin, Poland.

出版信息

Med Sci Monit. 2001 Nov-Dec;7(6):1236-41.

Abstract

BACKGROUND

The angiotensin-converting enzyme gene and the angiotensin II type 1 receptor gene meet the criteria for candidate genes in the pathogenesis of essential hypertension. The aim of this study was to assess the possible association between polymorphisms of these genes and essential hypertension in a Polish population, to evaluate them as possible genetic markers of susceptibility to hypertension, and to search for interaction between the two polymorphisms.

MATERIAL AND METHODS

The insertion/deletion polymorphism at the angiotensin-converting enzyme gene locus and the A1166C polymorphism at the angiotensin II type 1 receptor gene locus were detected using the polymerase chain reaction and restriction fragment length methods. 250 patients with stable essential hypertension lasting at least 1 year were compared to 150 individuals without signs and symptoms of cardiovascular disease or family history of hypertension.

RESULTS

No association was found between the insertion/deletion polymorphism at the angiotensin-converting enzyme locus and essential hypertension in the study population, although the DD genotype occurred more often (p<0.01) among patients with hypertension and a negative family history of hypertension than among hypertensives with a positive family history. There was an association in our study population between hypertension and the A1166C polymorphism at the angiotensinogen II type 1 receptor gene locus. The frequency of occurrence of the C1166 variant was higher among patients with hypertension (0.29) than in control subjects (0.20). The CC genotype occurred more frequently among hypertensives (0.10) than in the control group (0.04). Both these differences were statistically significant. This association was stronger in males, patients with a negative family history of hypertension, and non-obese patients with a body mass index less than 26 kg/m2. To test the interaction between the polymorphisms in question, the distribution of the A1166 and C1166 variants among ACE genotypes was assessed. The A1166 variant occurs more often among DD genotype normotensives.

CONCLUSIONS

There was no association in our study population between essential hypertension and the I/D polymorphism at the angiotensin-converting enzyme gene locus. The C1166 variant of the angiotensin II type 1 receptor gene was associated with hypertension in our study population, while the A1166 variant seems to be protective as regards susceptibility to hypertension.

摘要

背景

血管紧张素转换酶基因和血管紧张素II 1型受体基因符合原发性高血压发病机制中候选基因的标准。本研究的目的是评估这些基因的多态性与波兰人群原发性高血压之间的可能关联,将它们作为高血压易感性的可能遗传标记进行评估,并寻找两种多态性之间的相互作用。

材料与方法

采用聚合酶链反应和限制性片段长度方法检测血管紧张素转换酶基因位点的插入/缺失多态性和血管紧张素II 1型受体基因位点的A1166C多态性。将250例持续至少1年的稳定原发性高血压患者与150例无心血管疾病体征和症状或无高血压家族史的个体进行比较。

结果

在研究人群中,血管紧张素转换酶位点的插入/缺失多态性与原发性高血压之间未发现关联,尽管在高血压且家族高血压史阴性的患者中,DD基因型出现的频率更高(p<0.01),高于家族高血压史阳性的高血压患者。在我们的研究人群中,高血压与血管紧张素原II 1型受体基因位点的A1166C多态性之间存在关联。高血压患者中C1166变体的出现频率(0.29)高于对照组(0.20)。CC基因型在高血压患者中出现的频率(0.10)高于对照组(0.04)。这两个差异均具有统计学意义。这种关联在男性、家族高血压史阴性的患者以及体重指数小于26 kg/m2的非肥胖患者中更强。为了测试所讨论的多态性之间的相互作用,评估了A1166和C1166变体在ACE基因型中的分布。A1166变体在DD基因型正常血压者中出现的频率更高。

结论

在我们的研究人群中,原发性高血压与血管紧张素转换酶基因位点的I/D多态性之间无关联。血管紧张素II 1型受体基因的C1166变体与我们研究人群中的高血压相关,而A1166变体似乎对高血压易感性具有保护作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验