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血管紧张素转换酶基因插入/缺失多态性对血压的吸烟依赖性影响。

Smoking-dependent effects of the angiotensin-converting enzyme gene insertion/deletion polymorphism on blood pressure.

作者信息

Schut Anna F C, Sayed-Tabatabaei Fakhredin A, Witteman Jacqueline C M, Avella Aida M Bertoli, Vergeer Jeannette M, Pols Huibert A P, Hofman Albert, Deinum Jaap, van Duijn Cornelia M

机构信息

Departments of Epidemiology and Biostatistics, Erasmus Medical Center Rotterdam, The Netherlands.

出版信息

J Hypertens. 2004 Feb;22(2):313-9. doi: 10.1097/00004872-200402000-00015.

DOI:10.1097/00004872-200402000-00015
PMID:15076189
Abstract

BACKGROUND

Studies on the role of the angiotensin-converting enzyme (ACE) gene in the development of hypertension have yielded conflicting results. Recent studies suggested that this gene might have smoking-dependent effects on the development of cardiovascular disease.

OBJECTIVE

To study the relationship between the ACE insertion/deletion (I/D) polymorphism, blood pressure and risk of hypertension in current, former and non-smokers in a population-based cohort.

METHODS

We included 2412 non-smokers, 2794 former smokers and 1508 current smokers, all participants in the Rotterdam Study. In each group, we assessed the relationship between the ACE I/D polymorphism, systolic (SBP) and diastolic (DBP) blood pressures and risk of hypertension. Mean blood pressures and prevalence of hypertension were compared between carriers and non-carriers of the D allele. All analyses were adjusted for age, sex, body mass index, diabetes mellitus, high-density lipoprotein cholesterol, total cholesterol and use of antihypertensive medication.

RESULTS

In non-smokers and former smokers, blood pressure and the risk of hypertension did not differ significantly between genotypes. In smokers, we found a significant increase in SBP in DD carriers (139.6 +/- 22.8 mmHg) compared with II carriers (136.0 +/- 22.7 mmHg) (P = 0.04). No effect of ACE genotype was observed for DBP. The risk of hypertension was significantly increased in smokers who carried one [odds ratio (OR) 1.4, 95% confidence interval (CI) 1.0 to 1.9; P = 0.05] or two (OR 1.5, 95% CI 1.1 to 2.2; P = 0.02) copies of the D allele.

CONCLUSIONS

The D allele of the ACE polymorphism is associated with a significantly increased SBP and risk of hypertension in smokers. Our study underlines the importance of gene-environment interactions in the study of candidate genes for hypertension.

摘要

背景

关于血管紧张素转换酶(ACE)基因在高血压发生中的作用的研究结果相互矛盾。近期研究表明,该基因可能对心血管疾病的发生具有吸烟依赖性影响。

目的

在一个基于人群的队列中,研究目前吸烟者、既往吸烟者和从不吸烟者中ACE插入/缺失(I/D)多态性、血压与高血压风险之间的关系。

方法

我们纳入了鹿特丹研究的2412名从不吸烟者、2794名既往吸烟者和1508名目前吸烟者。在每组中,我们评估了ACE I/D多态性、收缩压(SBP)和舒张压(DBP)与高血压风险之间的关系。比较了D等位基因携带者和非携带者的平均血压及高血压患病率。所有分析均根据年龄、性别、体重指数、糖尿病、高密度脂蛋白胆固醇、总胆固醇和抗高血压药物的使用情况进行了校正。

结果

在从不吸烟者和既往吸烟者中,不同基因型之间的血压和高血压风险无显著差异。在吸烟者中,我们发现DD携带者的SBP(139.6±22.8 mmHg)显著高于II携带者(136.0±22.7 mmHg)(P = 0.04)。未观察到ACE基因型对DBP有影响。携带一个(比值比[OR] 1.4,95%置信区间[CI] 1.0至1.9;P = 0.05)或两个(OR 1.5,95% CI 1.1至2.2;P = 0.02)D等位基因拷贝的吸烟者患高血压的风险显著增加。

结论

ACE多态性的D等位基因与吸烟者SBP显著升高及高血压风险增加相关。我们的研究强调了基因-环境相互作用在高血压候选基因研究中的重要性。

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