Postgraduate Program in Nursing & Health, State University of Southwest Bahia (UESB), Jequie, BA, Brazil.
Department of Biological Sciences, Integrative Physiology Research Center, State University of Southwest Bahia (UESB), Jequie, BA, Brazil.
J Clin Hypertens (Greenwich). 2018 Mar;20(3):541-550. doi: 10.1111/jch.13224. Epub 2018 Mar 9.
The angiotensin-converting enzyme insertion/deletion (I/D) gene polymorphism has been widely reported as being associated with hypertension; however, most studies do not consider environmental/behavioral factors. This study aimed to investigate the relationship among angiotensin-converting enzyme insertion/deletion gene polymorphism, environmental/behavioral factors, and hypertension in community-dwelling elderly individuals. All community-dwelling older adults from Aiquara, Bahia, Brazil, were invited to take part in this study. After exclusions, 234 elderly participants were submitted to a data collection, which included sociodemographics, lifestyle and health status questionnaires, clinical assessment, and blood withdrawal. From the blood samples, the gene polymorphism was identified through polymerase chain reaction and patients grouped as II or D allele carriers (ID and DD genotypes). Hypertension was defined by self-report of the condition and confirmed by antihypertensive drug treatment. Chi-square test was used to identify differences in the proportions distributed between groups of each dependent variable (ie, genotype, diagnosis of hypertension, and blood pressure state from medicated patients with hypertension). The prevalence of hypertension was 59.3% and was associated with diabetes mellitus and obesity, but not with angiotensin-converting enzyme insertion/deletion gene polymorphism. However, carriers of the II genotype, a salt-sensitivity genotype, exhibited a significantly greater estimated sodium intake. In addition, among medicated elderly patients with hypertension, II genotype carriers exhibited poor blood pressure control, despite similar antihypertensive drug treatment in D allele carriers, while exhibiting a greater estimated sodium intake. Our results provide new evidence regarding the interaction of genetic and environmental/behavioral factors in the genesis of hypertension among elderly patients, as well as in blood pressure control in medicated elderly patients with hypertension.
血管紧张素转换酶插入/缺失(I/D)基因多态性与高血压广泛相关;然而,大多数研究都不考虑环境/行为因素。本研究旨在探讨血管紧张素转换酶插入/缺失基因多态性、环境/行为因素与社区老年人高血压之间的关系。巴西巴伊亚州 Aiquara 的所有社区老年人都被邀请参加这项研究。排除后,234 名老年人接受了一项数据收集,其中包括社会人口统计学、生活方式和健康状况问卷、临床评估和血液采集。从血液样本中,通过聚合酶链反应确定基因多态性,将患者分为 II 或 D 等位基因携带者(ID 和 DD 基因型)。高血压通过自我报告该疾病并通过抗高血压药物治疗来确认。卡方检验用于识别每个因变量(即基因型、高血压诊断和高血压药物治疗患者的血压状态)组之间分布比例的差异。高血压的患病率为 59.3%,与糖尿病和肥胖有关,但与血管紧张素转换酶插入/缺失基因多态性无关。然而,II 基因型携带者是一种盐敏感性基因型,其估计的钠摄入量明显更高。此外,在接受药物治疗的高血压老年患者中,II 基因型携带者尽管在 D 等位基因携带者中接受了类似的抗高血压药物治疗,但血压控制较差,同时表现出更高的估计钠摄入量。我们的结果提供了新的证据,表明遗传和环境/行为因素在老年患者高血压的发生以及高血压药物治疗的老年患者血压控制中的相互作用。