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首页> 外文期刊>Journal of hypertension >Influence of cardiovascular risk factors on relation between angiotensin converting enzyme-gene polymorphism and blood pressure in arterial hypertension.
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Influence of cardiovascular risk factors on relation between angiotensin converting enzyme-gene polymorphism and blood pressure in arterial hypertension.

机译:心血管危险因素对动脉高血压中血管紧张素转化酶基因多态性与血压之间关系的影响。

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摘要

BACKGROUND: The angiotensin-converting enzyme gene insertion (I)/deletion (D) polymorphism might be involved in the development of several cardiovascular diseases, but its role in humans remains controversial. OBJECTIVE: To investigate the relation between the angiotensin converting enzyme gene polymorphism and extent of blood pressure elevation in arterial hypertension, taking into account the influence of cardiovascular risk factors. METHODS: We studied 171 patients (aged 49 +/- 9 years, 61 women) with abnormal clinic and 24 h ambulatory blood pressures, after a 3-week wash-out. RESULTS: We found no significant difference in clinic and ambulatory blood pressures among homozygotic D (DD), heterozygotic D (ID) and homozygotic I (II) angiotensin converting enzyme genotypes and between homozygotic D (DD) and pooled heterozygotic D (ID) plus homozygotic I (II) (non-DD) angiotensin converting enzyme genotypes. At least one additional cardiovascular risk factor (smoking, hypercholesterolaemia or diabetes) was present for 103 patients (33 DD and 70 non-DD). Non-DD subjects (n = 43) without additional cardiovascular risk factors exhibited lower values of 24 h, daytime systolic and pulse blood pressures than did members of all other groups (all P < 0.04). In the presence of risk factors, DD and non-DD subjects exhibited similar systolic and pulse ambulatory blood pressures, in that we found higher values in non-DD genotype subjects with risk factors than we did for non-DD subjects without additional risk factors. In multivariate analysis, the combination of non-DD genotype and absence of cardiovascular risk factors was associated with the lowest values of systolic and pulse blood pressures. CONCLUSIONS: Angiotensin converting enzyme insertion allele appears clustered with lower ambulatory systolic and pulse blood pressures in hypertensive patients when the potential interference of additional cardiovascular risk factors is eliminated. A high prevalence of cardiovascular risk factors in population studies might blunt a possible biological association of blood pressure with DD genotype by contributing to raising of blood pressures also in subjects with non-DD genotypes.
机译:背景:血管紧张素转换酶基因插入(I)/缺失(D)多态性可能与几种心血管疾病的发展有关,但其在人类中的作用仍存在争议。目的:考虑心血管危险因素的影响,探讨血管紧张素转换酶基因多态性与高血压患者血压升高程度的关系。方法:我们对171名患者(49 +/- 9岁,61名女性)进行了3周的冲洗后,发现他们的诊所异常,24 h动态血压。结果:我们发现纯合D(DD),杂合D(ID)和纯合I(II)血管紧张素转化酶基因型以及纯合D(DD)和合并杂合D(ID)加之间的临床和门诊血压无显着差异纯合I(II)(非DD)血管紧张素转化酶基因型。 103例患者(33 DD和70例非DD)至少存在一种另外的心血管危险因素(吸烟,高胆固醇血症或糖尿病)。没有其他心血管危险因素的非DD受试者(n = 43)的24 h,白天的收缩压和脉搏血压值均低于所有其他组的受试者(所有P <0.04)。在存在危险因素的情况下,DD和非DD受试者表现出相似的收缩压和脉动动态血压,因为我们发现具有危险因素的非DD基因型受试者的价值高于没有其他危险因素的非DD受试者。在多变量分析中,非DD基因型和无心血管危险因素的组合与最低的收缩压和脉搏血压有关。结论:在消除了其他心血管危险因素的潜在干扰后,高血压患者的血管紧张素转化酶插入等位基因似乎聚集在较低的动态收缩压和脉搏血压中。在人群研究中,心血管危险因素的高患病率可能会通过导致非DD基因型受试者的血压升高而抑制血压与DD基因型的生物学联系。

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