Forrester T, McFarlane-Anderson N, Bennett F I, Wilks R, Cooper R, Rotimi C, Morrison L, Ward R
Tropical Metabolism Research Unit, University of the West Indies, Mona, Jamaica.
Am J Hypertens. 1997 May;10(5 Pt 1):519-24. doi: 10.1016/s0895-7061(97)00049-6.
An insertion/deletion (I/D) polymorphism of the angiotensin I converting enzyme gene influences the level of serum angiotensin converting enzyme activity and has been associated with risk of several cardiovascular conditions. The relationship to blood pressure remains uncertain, however. We conducted a population-based survey in Kingston, Jamaica, to examine the association between angiotensin converting enzyme genotype, angiotensin converting enzyme serum activity and blood pressure. Serum angiotensin converting enzyme activity was measured and genotyping performed for the I/D polymorphism in 500 community residents. The overall prevalence of the D allele was 59.3%. Angiotensin converting enzyme genotype was not significantly related to blood pressure (P = .16), although it did influence angiotensin-converting enzyme activity, leading to an increase of 35% among individuals with the DD as compared with II genotype. Angiotensin converting enzyme levels were significantly higher in hypertensives as compared with normotensives (P < .05). A modest correlation was observed between blood pressure and angiotensin converting enzyme activity among untreated individuals (r = 0.11; P = .04), although this did not persist in multivariate analysis. A relationship between body mass index and angiotensin converting enzyme activity was identified in both men and women that was independent of genotype. These data demonstrate findings among blacks which are consistent with other studies and suggest a relationship between angiotensin converting enzyme genotype, and serum activity which is influenced by both genetic and environmental factors. The potential role of ACE on blood pressure control in the population remains uncertain.
血管紧张素I转换酶基因的插入/缺失(I/D)多态性会影响血清血管紧张素转换酶活性水平,并与多种心血管疾病的风险相关。然而,其与血压的关系仍不明确。我们在牙买加金斯敦进行了一项基于人群的调查,以研究血管紧张素转换酶基因型、血管紧张素转换酶血清活性与血压之间的关联。对500名社区居民测量了血清血管紧张素转换酶活性,并对I/D多态性进行基因分型。D等位基因的总体患病率为59.3%。血管紧张素转换酶基因型与血压无显著相关性(P = 0.16),尽管它确实会影响血管紧张素转换酶活性,与II基因型个体相比,DD基因型个体的活性增加了35%。高血压患者的血管紧张素转换酶水平显著高于血压正常者(P < 0.05)。在未经治疗的个体中,观察到血压与血管紧张素转换酶活性之间存在适度的相关性(r = 0.11;P = 0.04),尽管在多变量分析中这种相关性未持续存在。在男性和女性中均发现体重指数与血管紧张素转换酶活性之间存在一种独立于基因型的关系。这些数据表明黑人中的研究结果与其他研究一致,并提示血管紧张素转换酶基因型和血清活性之间存在一种受遗传和环境因素影响的关系。血管紧张素转换酶在人群血压控制中的潜在作用仍不明确。