Angiotensin-converting enzyme insertion/deletion polymorphism, 24-h blood pressure profile and left ventricular hypertrophy in hypertensive individuals: a cross-sectional study

Hypertension (HT) is a highly prevalent disease associated with increased risk of target organ damage (TOD), including myocardial infarction, stroke and left ventricular hypertrophy (LVH). Changes in blood pressure are influenced by daily activities and interactions with neurohumoral, behavioral and environmental factors. Under physiological conditions, there is a drop in the blood pressure (BP) between wakefulness and sleep, a phenomenon known as nocturnal blood pressure dipping (ND). The absence of ND is associated with TOD and higher mortality [1‐4].

Due to the multifactorial etiology of HT, many researchers are studying the association between genetic polymorphisms and HT and its complications. This research studied the angiotensin-converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism, which is characterized by the presence (insertion) or absence (deletion) of an Alu repetitive sequence of 287 base pairs (bp) in intron 16 of the ACE gene [5]. The variability in plasma ACE levels is directly related to the I/D polymorphism; the I allele is associated with a reduced level of this enzyme and lower concentrations of angiotensin II in tissues [5], a condition that apparently protects against TOD.

The ACE I/D polymorphism is linked to risk for myocardial infarction and cardiovascular events [6‐9], LVH [10‐12], microalbuminuria [11, 13, 14], thoracic aortic aneurysm in patients with bicuspid or tricuspid aortic valves [15], pregnancy hypertensive disorders [16, 17], and hypertensive emergency [18]. Moreover, this polymorphism is related to inter-individual differences in BP response, for example, a low dose of the hydrochlorothiazide diuretic produced greater BP reductions in men with the DD genotype and women with the II genotype [19]. Therefore, this polymorphism may also have a role in the genesis of TOD, which is commonly found in hypertensive individuals. Recently, a meta-analysis of 44 articles involving 12,616 subjects, demonstrated the contribution of the I/D polymorphism to susceptibility for LVH [20].

The findings reported in the literature in respect to the relationship of this polymorphism with BP levels and TOD are controversial [14, 21‐31]. Thus, this study aimed to characterize the anthropometric, biochemical, and echocardiographic data and blood pressure profile of non-diabetic hypertensive individuals and to investigate the influence of the ACE I/D polymorphism on 24-h BP levels and on TOD.

This project was approved by the Research Ethics Committee of the State Medical School in São José do Rio Preto (no. 169/2008). All participants were informed about the purpose of the work and gave their written informed consent before participating in the research. This was a cross-sectional study, which enrolled 155 hypertensive individuals followed-up at a university hospital outpatient clinic. The exclusion criteria were age under 40 years, history of valvular disease, systolic/diastolic dysfunction, diabetes mellitus (DM), body mass index (BMI) ≥35 kg/m², creatinine clearance <30 mL/min/m², and secondary hypertension.

An investigative protocol was used to collect information on age, gender, medicines taken, and comorbidities. Data regarding DM, strokes, MI, and dyslipidemia (DLP) were used to assess comorbidities. Patients who had presented with two or more fasting glycemia levels ≥126 mg/dL or altered oral glucose tolerance test (≥200 mg/dL) were excluded [32]. History of strokes was based on clinical history, medical records, and the presence of sequels. The diagnosis of MI was based on clinical history and confirmed by an analysis of medical records that described enzymatic alterations (troponin and CK-MB), and electrocardiographic alterations suggestive of coronary ischemia and treatment. DLP was identified by total cholesterol (TC), high-density lipoprotein cholesterol fraction (HDL-c) and triglycerides (TG) levels after 12 h of fasting [33]. The following reference values were adopted: TC <200 mg/dL, HDL-c >40 mg/dL, low-density lipoprotein cholesterol fraction (LDL-c) <130 mg/dL and TG <150 mg/dL. The LDL-c fraction was calculated using the formula: LDL-c = TC − HDL-c − TG/5 (for TG <400 mg/dL) [34]. DLP was defined for individuals with alterations in the aforementioned parameters and those who were under treatment with HMG-CoA reductase inhibitors or other hypolipemic drugs.

Weight and height were measured and BMI was calculated using the formula: BMI = weight (kg)/height (m)². Besides stroke and MI, TOD was also considered as the presence of microalbuminuria and left ventricular hypertrophy (LVH). Microalbuminuria was characterized as the average of two 24-h urinary albumin excretion rates ≥20 μg/min.

The anthropometric, biochemical, and echocardiographic data and blood pressure profile of the sample are presented in Table 1. The mean time of HT (16.0 ± 10.1 years), BP levels above the recommended range, and increased values of BMI (28.8 ± 4.9 kg/m²) and microalbuminuria (58.1 %) stand out in this sample. On comparing individuals with and without ND, there were no differences between clinical, and biochemical variables or TOD except for lower BP levels during sleep (p < 0.001) in patients with ND (Table 2). There was not systolic and diastolic ventricular dysfunction and neither significant areas of infarction scars in the evaluated sample.

When grouped according to the genotype of the ACE I/D polymorphism, the groups did not significantly differ in respect to mean age, gender, BMI and duration of HT. There were no statistically significant differences between the three genotypes (II, ID, and DD) and mean 24-h BP by ABPM (Table 3). However, there was a significant difference in the prevalence of LVH between the ACE genotypes (II: 13.0 %; ID: 34.1 %; DD: 46.5 %; p value = 0.024). By logistic regression (Table 4), carriers of the DD genotype had higher risk of LVH compared to those with the II genotype (OR: 5.8; 95 % CI 1.50–22.44; p value = 0.011). There was no significant difference between genotypes in respect to the other TOD investigated in this study.

Carriers of the D allele (ID and DD genotypes) had higher awake systolic BP and mean 24-h BP compared to those with the II genotype (p value = 0.036 and p value = 0.042, respectively) (Table 3) although there were no statistically significant differences between the three genotypes. Moreover, carriers of the D allele also had higher left ventricular mass (209.3 ± 87.1 vs. 170.1 ± 48.0 g; p value = 0.003), left ventricular mass index (117.3 ± 50.0 vs. 100.3 ± 25.7 g/m²; p value = 0.017) and, consequently, higher prevalence of LVH (37.4 vs. 12.5 %; p value = 0.019) than individuals with the II genotype. By logistic regression, D allele carriers had a three times higher risk of LVH than those with the II genotype (OR = 4.14; 95 % CI 1.17–14.65; p value = 0.028) (Table 4). The allelic and genotypic distributions of the population were in balance according to the Hardy–Weinberg equilibrium (χ ² = 3.11; p > 0.05).

This study demonstrates an association between the D allele of the ACE I/D polymorphism and increased BP, and a correlation of the DD genotype with higher prevalence of LVH in non-diabetic hypertensive patients who despite antihypertensive treatment have poorly controlled BP.

Recently, there has been growing interest in association studies on the I/D polymorphism and ACE plasma levels and, consequently, on angiotensin II concentrations. However, results of studies on this relationship in hypertensive patients are controversial. Thus, while some case–control studies did not confirm any association between the I/D polymorphism and HT [21, 23, 24, 27, 41], others reported a higher frequency of the D allele [28, 31] and DD genotype in subjects with HT [22, 28‐30]. In these cases, it is possible that the profile of the sample regarding age, gender and associated diseases may have influenced the distribution of ACE genetic variants. In fact, studies performed in several countries have confirmed this association [22, 28‐30]. In a Japanese population, one study found higher systolic BP in subjects aged ≥50 years with the ID genotype compared to II carriers, and higher diastolic BP in individuals with the ID and DD genotypes compared to those with the II genotype [25]. Among the possible explanations for these differences, is that BP increases with age, which may have influenced the polymorphism studied [42].

In the current study, an association was found between the D allele and higher systolic BP during wakefulness and during 24-h ABPM in treated patients, results that are not supported by some other authors [21, 23, 41]. On the other hand, higher BP levels were demonstrated for all evaluated periods (wake, sleep and 24-h) in elderly hypertensive Japanese patients who had the D allele [43]. In addition, Julve et al. [44] reported slightly higher BP levels in patients with the DD genotype, due to higher BP during the nighttime and thus less nocturnal dipping. Although some authors demonstrated this association only in males [22, 45], the authors of a meta-analysis found 79 % greater risk of hypertension in females with the DD compared to those with the II genotype [13].

In the present study, the ACE I/D polymorphism had no influence on ND, which corroborates the results of other authors [21, 23] although one study demonstrated a smaller drop between awake and sleep BP in hypertensive patients with the DD genotype in comparison to carriers of the I allele [44]. In addition, there was no effect of ACE I/D polymorphism or serum ACE levels on circadian variability of blood pressures among pediatric renal transplant patients [46] and in patients with type 1 diabetes [47].

In relation to the association between the ACE I/D polymorphism and TOD in hypertensive individuals, the current research shows that individuals with the DD genotype had an almost fivefold higher risk for LVH compared to those with the II genotype, a condition reported by previous studies [10, 11]. Recently, two meta-analyses demonstrated an association between the ACE I/D polymorphism and LVH [20, 48]. However, other authors did not confirm this association [49, 50]. These conflicting results may reflect the influence of ethnicity, comorbidities, and even of antihypertensive treatment on the ACE I/D polymorphism and TOD associated with HT.

There is evidence that hypertensive patients with the DD genotype present the best antihypertensive response to medications, especially in respect to renin–angiotensin system (RAS) blockers [51, 52]. These studies demonstrated a genetic influence on response to BP treatment, and the effect of RAS blockers on the regression of LVH. Recently, another investigation demonstrated individuals presented with emergency hypertensive (HE) characterized by TOD had a lower frequency of the II genotype and less use of RAS blockers when compared with the hypertensive urgency group, characterized as no TOD. Thus, the risk of an individual having HE was increased in the presence of these two conditions (low frequency of the II genotype and less use of RAS blockers) [18]. On the other hand, one study demonstrated the effect of ramipril in inflammatory response in patients undergoing coronary artery bypass grafts without the ACE I/D gene polymorphism influence [53].

It is known that TOD is more related to the mean 24-h BP levels than office BP levels [1, 2], which highlights the need for ABPM to evaluate hypertensive patients. The absence of ND seems to correlate with TOD in hypertensive individuals [54], although this result was not found in the current study.

In the present study, the DD genotype was associated to higher risk of LVH compared to the II genotype, which suggests that the ACE I/D polymorphism may be more important than ND in the genesis of LVH. In favor of this hypothesis, the results of a meta-analysis found a greater risk for LVH associated with the D allele or DD genotype in untreated hypertensive patients [20]. In addition, DD genotype was also independently associated with worse echocardiographic outcome in patients with non-ischemic heart failure [55]. This is related to an increased neurohormonal response, mainly of the renin–angiotensin aldosterone system [56]. So, it is important to point that LVH is an early TOD associated to cardiac insufficiency. These facts suggest that independent of the treatment, LVH occurs more frequently in individuals with the D allele or DD genotype. Thus, it is important to highlight that it is possible to detect the impact of genetic load on the cardiac phenotype, even with pharmacological treatment.

Some limitations of this study should be mentioned. First, the size of the sample was small, in part, because of the difficulty to select patients due to the exclusion criteria. Second, it was not possible to exclude patients with obstructive sleep apnea, a fact that may influence the frequency of LVH. However, we have excluded patients with BMI ≥35 kg/m², which reduces greatly the possibility of sleep apnea. Finally, the lack of a control group of normotensive individuals, in our viewpoint, was the main limitation of this study. Besides, we can cite two strong points. The study population was separated in two groups, according to nocturnal dipping and the investigation of influence of the ACE I/D polymorphism on 24-h BP levels and on target organ damage.

To our knowledge, this is the first study that evaluates the ACE I/D polymorphism in respect to ABPM and TOD in Brazilian hypertensive patients. The present study reports two findings: the presence of the D allele of the ACE I/D polymorphism is correlated with higher mean 24-h systolic BP and wake systolic BP, and the DD genotype is associated with higher prevalence of LVH in non-diabetic hypertensive patients on antihypertensive treatment.