Prevention of atrial fibrillation with renin-angiotensin system inhibitors on essential hypertensive patients: a meta-analysis of randomized controlled trials.

We aimed to investigate the effectiveness and safety of angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin II receptor blockers (ARBs) on preventing atrial fibrillation in essential hypertensive patients. Systematic literature retrieval was carried out to obtain randomized controlled trials on the effects of ACEI/ARBs on essential hypertensive patients before December, 2013. Data extraction and quality evaluation were performed. Meta-analysis was performed by Review Manager 5.2.3. Ten high quality studies (11 articles) with a total of 42,892 patients (20,491 patients in the ACEI/ARBs group and 22,401 patients in the β-blocker or the calcium antagonist group) met the inclusion criteria and were included in the meta-analysis. The results showed that ACEI/ARBs reduced the incidence of atrial fibrillation (AF) recurrence compared to calcium antagonists (RR = 0.48; 95%CI, 0.40-0.58; P<0.00001) or β-blockers (RR = 0.39; 95%CI, 0.20-0.74; P = 0.005) in long-term follow-up, respectively. Furthermore, ACEI/ARBs reduced the incidence of congestive heart failure (RR = 0.86; 95%CI, 0.77-0.96; P = 0.007). However, no significant effects were observed on the incidence of new AF, cardiac death, myocardial infarction, and stroke. Our results suggest that ACEI/ARBs may reduce the incidence of AF recurrence and congestive heart failure, with fewer serious adverse effects.

Introduction

Hypertension is one of the most prevalent and powerful contributors to cardiovascular diseases, especially stroke, the leading cause of death all over the world[. Atrial fibrillation (AF), a common complication of hypertension, is associated with an increased risk of morbidity and mortality[. Although medication for hypertention has been well developed, a large number of well-controlled hypertensive patients still suffer from AF. Therefore, finding a more effective way of preventing AF is important for improving the prognosis of patients with essential hypertension.

Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin II receptor blockers (ARBs) are two commonly used antihypertensives, which prevent cardiac structural remodeling and electrical remodeling. AF activates the renin-angiotensin system (RAS), which in turn promotes atrial fibrosis, atrial electrophysiological and structural remodeling, and subsequently facilitates the recurrence of AF[. Thus, ACEI/ARBs may theoretically attenuate deleterious cardiac remodeling and reduce the recurrence of AF[. However, the results of different studies are controversial. Jibrini et al.[ found that patients with hypertension benefited from treatment of ACEI/ARBs on reducing the relative risk of AF by 23%, while the other two groups found no benefits[.

To further investigate the efficacy and safety of RAS inhibitors in preventing AF, we performed a meta-analysis of randomized controlled trials. Our results may provide more powerful evidence for clinicians.

Methods

Literature search

Following the methodological guidelines in Cochrane Reviewer's Handbook (Version 5.1.0), 3 databases including PubMed (1966-2013.12), Embase (1974-2013.12) and the Cochrane Library (Issue 12, 2013) were searched with the following words: "Angiotensin-Converting Enzyme Inhibitors" [Mesh/Emtree], Angiotensin Converting Enzyme Inhibitor*, "Angiotensin II Type 1 Receptor Blockers" [Mesh/Emtree], "angiotensin receptor", ACE, ACEI, ACE-I, ACEs, captopril, enalapril, fosinopril, lisinopril, perindopril, ramipril, quinapril, benazepril, cilazapril, trandolapril, spirapril, delapril, moexipril, zofenopril, imidapril, AT 2 receptor block*, AT 2 receptor antagon*, ARB, ARBs, candesartan, eprosartan, irbesartan, losartan, olmesartan, telmisartan, valsartan, Hypertension, "Hypertension"[Mesh/Emtree], "Atrial Fibrillation" [Mesh/Emtree], and "Atrial Flutter" [Mesh/Emtree]. The process did not set limit. In addition, the references of the retrieved literature were also manually checked to filter potentially eligible studies. Last search reached December, 2013.

Criteria for considering trials for this review

Inclusion criteria

Randomized control trials (RCTs) only, detailed information about random sequence generation, allocation concealment and blinding were not considered. All patients entering the studies needed to meet the following criteria with no restriction of age suffering from essential hypertension, which was defined as systolic blood pressure (SBP) ≥140 mmHg and/or diastolic blood pressure (DBP) ≥90 mmHg. The patients should remain in sinus rhythm but with at least one electrocardiogram (ECG)-documented episode of symptomatic or paroxysmal AF during 6 months before randomization. Particularly, we also included trials in which patients suffered essential hypertension without AF. These patients were thus at risk of developing AF. The ACEI/ARB group received ACEIs or ARBs, and the control group received placebo or positive drugs, such as β-blockers and calcium antagonists. Primary endpoints: incidence of new AF or AF recurrence during follow-up. Secondary endpoints: cardiovascular events, including cardiac death, myocardial infarction, cerebral infarction, congestive heart failure, and adverse effects (bradycardia, atrial flutter, intolerable and unproductive cough, peripheral edema and dizziness) during follow-up.

Exclusion criteria

Trials in the following categories were excluded, including non-randomized controlled trials, subjects who were not treated with ACEI or ARB, and trials with no mentioning of AF prevention.

Data extraction

According to previously defined data-extraction form, 2 investigators (D-Z and Z-MW) independently read the titles, abstracts and full texts, using the following steps: (1) examining titles and abstracts to remove obviously irrelevant studies, (2) retrieving the full texts of potentially relevant trials, (3) examining full texts for compliance of studies with eligibility criteria, and (4) making final decisions on study inclusion and proceeding to data collection. Baseline information of patients and detailed methods of study designs were extracted from included studies. Disagreement was solved by discussion with others (D-Z and Z-MW).

Quality evaluation

Evaluation of methodological quality was based on criteria described in Cochrane Reviewer's Handbook 5.1.0. It contains random sequence generation, allocation concealment, blinding, and incomplete outcome data. Each study was subjected to quality assessment by 2 investigators (D-Z and Z-MW). For unclear information for study design or data, investigator contacted the author by E-mail.

Statistical analysis

Differences were expressed as risk ratios (RRs) and odd ratio (ORs) with 95% confidence intervals (95%CIs) for dichotomous outcomes and standardized mean differences (SMDs) with 95%CIs for continuous outcomes. Heterogeneity across studies was tested by using the I2 statistic, which is a quantitative measure of inconsistency across studies. Studies with an I2 statistic of 25%-50% were considered as low heterogeneity, those with an I2 statistic of 50%-75% had moderate heterogeneity, and those with an I2 statistic of >75% had a high degree of heterogeneity[. An I2 value >50% indicated significant heterogeneity. A fixed-effects model was used, and a random-effects model was used in the case of significant heterogeneity (I2>50%)[. We further conducted sensitivity analyses to explore possible explanations for heterogeneity on the overall pooled estimate and to examine influence of various exclusion criteria on the overall pooled estimate. Differences were considered statistically significant at P<0.05. All statistical analyses were performed by Review Manager Software (Version 5.2.3, Cochrane Collaboration).

Results

Process for included trials

As shown in , a total of 863 potentially relevant studies were identified and screened for retrieval. After reading titles and abstracts, 433 studies were excluded due to duplications, reviews, case reports and animal experiments. Then, 380 studies were excluded after reading the abstracts in more detail. Among the remaining 50 studies, 39 studies were excluded because they included non-hypertensive patients or did not report interesting outcomes. Finally, 11 studies[ were included in our review. As the studies of Julius et al.[ and Schmieder et al.[ are the same trial in different time, we included them as one study.

Fig. 1

Flowchart of studies included in the meta-analysis.

Characteristics of included trials and quality evaluation

Main characteristics of the trials included in our meta-analysis are shown in . There were 20,491 hypertensive patients in the ACEI/ARBs group, and 22,401 patients in the β-blocker or calcium antagonist group. Six studies[ included outpatients with mild essential hypertension and at least one ECG-documented episode of symptomatic or paroxysmal AF in the previous 6 months before randomization. Four studies[ included hypertensive patients without a history of AF. Seven studies[ compared the efficiency between ACEI/ARBs and calcium antagonists, and 4 studies[ compared the efficiency between ACEI/ARBs and β-blockers. Duration of follow-up varied from 3 months to 73.2 months.

Table 1

Characteristics of included trials.

Study	Drugs and Dose	No. of patients	Female	Mean Age (years)	Definition of Hypertension	Study Population	How AF was Diagnosed	Follow-Up (Months)
Hansson 1999 (STOP-2)
ACEI/ARB	Enalapril 10 mg/day, Lisinopril 10 mg/day	2205	1462	76.1				60
Conventional drugs	Atenolol 50 mg/day, Metoprolol 100 mg/day, Pindolol 5 mg/day	2213	1505	76.0	SBP≥180 mmHg, DBP≥105 mmHg, or both	Patients who had treated or untreated primary hypertension	Yearly ECG and if symptoms
Calcium antagonists	Felodipine 2.5 mg/day, Isradipine 2.5 mg/day	2196	1449	75.9
Yamashita 2011
ACEI/ARB	Candesartan 8.0±2.7 mg/day	158	49	66.0	SBP≥140 mmHg and/or DBP≥90 mmHg, or requiring any treatment at enrolment	Patients with a history of paroxysmal AF within 6 months and hypertension or requiring any hypertension treatment at enrolment	A transtelephonic monitoring device which was requested to transmit ECG records and any arrhythmia-related symptoms every day to a central service	12
Calcium antagonists	Amlodipine 4.3±1.7 mg/day	160	50	65.1
Hansson 1999 (CAPPP)
ACEI/ARB	Captopril 50 mg/day	5492	2476	52.4				73.2
Conventional drugs	Atenolol and Metoprolol 50-100 mg/day	5493	2635	52.7	DBP≥100 mmHg	Patients who had treated or untreated primary hypertension	ECG during follow-up visits
Fogari 2006
ACEI/ARB	Losartan 50 mg/day	111	48	63.5	SBP>140 mmHg and/or 90 mmHg<DBP<100 mmHg	Outpatients with mild essential hypertension and at least 2 ECG-documented episodes of symptomatic AF in the previous 6 months and in treatment with a maintenance dose of amiodarone for at least 8 weeks	To identify a symptomatic AF episodes, 24-hour ambulatory ECG monitoring was performed every 4 weeks by using a Syneflash Holter recorder by ElaMedical Inc.	3
Calcium antagonists	Amlodipine 5 mg/day	111	50	63.2
Wachtell 2005
ACEI/ARB	Losartan 50 mg/day	4298	2125	57.6	160 mmHg<SBP< 200 mmHg and/or 95 mmHg<DBP<115 mmHg	Patients with previously treated or untreated hypertension and ECG signs of left ventricular hypertrophy, without a history of AF	New-onset AF was identified from annual in-study ECGs that underwent Minnesota coding for AF at a single ECG core center	57.6
Conventional drugs	Atenolol 50 mg/day	4182	2084	57.6
Fogari 2012
ACEI/ARB	Telmisartan 80-160 mg/day	188	101	68.5	140 mmHg<SBP< 160 mmHg and/or 90 mmHg<DBP<100 mmHg	Outpatients with stage I hypertension, in sinus rhythm, but with ≥2 ECG-documented episodes of symptomatic AF in the previous 6 months, each lasting >60 minutes but <7days and terminating spontaneously	24-hour ambulatory ECG monitoring was performed using a Syneflash Holter recorder (ELA Medical, Paris, France) to detect asymptomatic AF episodes	3
Calcium antagonists	Amlodipine 5-10 mg/day	190	103	67.9
Galzerano 2012
ACEI/ARB	Telmisartan 80 mg/day	70	21	56.2	140 mmHg<SBP< 160 mmHg and/or 90 mmHg<DBP<100 mmHg	Mild hypertensive outpatients in sinus rhythm with 1 or more ECG-documented episodes of AF in the previous 6 months	When to palpitations and new symptoms, patients were asked to report any episodes of symptomatic AF and to have ECG evaluations performed as soon as possible	12
Conventional drugs	Carvedilol 25 mg/day	62	19	55.4
Du 2013
ACEI/ARB	Telmisartan 80 mg/day	74	31	61.5	140 mmHg<SBP< 180 mmHg and/or 90 mmHg<DBP<110 mmHg	All hypertensive patients with paroxysmal AF	The development of persistent AF implied AF had continued for>7 days but was terminated after pharmacological and electric conversion	24
Calcium antagonists	Nifedipine 30 mg/day	75	26	62.0
Julius 2004Schmieder 2008
ACEI/ARB	Valsartan 80-160 mg/day	7649	3240	67.2	160 mmHg<SBP< 210 mmHg and/or DBP<115 mmHg	Patients with treated or untreated hypertension	ECG during follow-up visits	50.4
Calcium antagonists	Amlodipine 5-10mg/day	7596	3228	67.3
Fogari 2008
ARB	Valsartan 160 mg/day	122	65	66.0	140 mmHg<SBP< 160 mmHg and/or 90 mmHg<DBP<100 mmHg	Outpatients with mild essential hypertension, in sinus rhythm but with at least 2 ECG documented episodes of symptomatic AF in the previous 6 months, and without any treatment	24-h ambulatory ECG monitoring was performed every 4 weeks using a Syneflash Holter recorder (ElaMedical, Paris, France) to identify asymptomatic AF episodes	3
ACEI	Ramipril 5 mg/day	124	67	64.0
Calcium antagonists	Amlodipine 5 mg/day	123	68	65.0

shows that the quality of studies in this meta-analysis was good. Five studies[ reported random sequence generation, which was from computerized randomization, and the rest were randomized controlled trials. Allocation concealment in detail was only reported in one study[. Six studies[ had open-label design. Six studies[ used the double-blind method, 1 study the single-blind method, and 2 studies[ applied masked-endpoint for evaluation. A total of 428 patients were lost to follow-up in 9 studies[.

Table 2

Quality evaluation of the studies in this meta-analysis.

Study	Random sequence generation	Allocation concealment	Blinding	Completeness of data	Intention to treat analysis
Hansson 1999(STOP-2)	Computerized randomization	Open-label	Masked-endpoint	No patient was lost	Yes
Yamashita 2011	Computerized randomization	Open-label	Double-blind	8 patients withdrew	Yes
Hansson 1999(CAPPP)	Computerized randomization	Open-label	Masked-endpoint	27 patients were lost	Yes
Fogari 2006	Unclear	Unclear	Double-blind	8 patients withdrew	Yes
Wachtell 2005	Unclear	Open-label	Double-blind	Unclear	Yes
Fogari 2012	Unclear	Unclear	Double-blind	27 patients were lost	Yes
Galzerano 2012	Unclear	Open-label	Single-blind	27 patients were lost	No
Du 2013	Computerized randomization	Open-label	Unclear	No patient was lost	No
Julius 2004Schmieder 2008	Computerized randomization	List was prepared centrally by the sponsor with appropriate blocks	Double-blind	251 patients were lost	Yes
Fogari 2008	Unclear	Unclear	Double-blind	80 patients were lost	Yes

Meta-analysis results

Primary endpoints

As shown in , ACEI/ARBs decreased the incidence of AF recurrence at 3 months (RR = 0.49; 95%CI, 0.34–0.72; P = 0.0003) and long-term follow-up (RR = 0.47; 95%CI, 0.39–0.47; P<0.00001), and the tests for heterogeneity in those subgroups were I2 = 0%, P = 0.89 and I2 = 0%, P = 0.65, respectively. However, ACEI/ARBs did not change the incidence of new AF in long-term follow-up (RR = 0.86; 95%CI, 0.69-1.07; P = 0.19), with a high heterogeneity (I2 = 81%, P = 0.001).

Fig. 2

Forest plot of ACEI/ARBs versus control on preventing AF recurrence and new AF in long-term follow-up.

We further performed sensitivity analyses to explore the stability of our results. After removal of 2 studies[ with modest sample sizes (n≤150), we still found that ACEI/ARBs decreased the incidence of AF recurrence in long-term follow-up (RR = 0.49; 95%CI, 0.40-0.59; P<0.00001) with low heterogeneity (I2 = 0%, P = 0.48). Changing effect size did not influence the pooled results substantially: AF recurrence at 3 months (OR = 0.45; 95%CI, 0.29-0.69; P = 0.0003), AF recurrence in long-term follow-up (OR = 0.34; 95%CI, 0.27-0.44; P<0.00001) and new AF in long-term follow-up (OR = 0.86; 95%CI, 0.68-1.08; P = 0.19), and the heterogeneity was (I2 = 0%, P = 0.93), (I2 = 0%, P = 0.80), and (I2 = 81%, P = 0.001), respectively.

When compared to the different control groups, the incidence of AF recurrence was lower in patients receiving ACEI/ARBs than in those receiving calcium antagonists in long-term follow-up (RR = 0.48; 95%CI, 0.40-0.58; P<0.00001; ) with low heterogeneity (I2 = 0%, P = 0.57). However, ACEI/ARBs did not reduce new AF in long-term follow-up (RR = 0.96; 95%CI, 0.74-1.24; P = 0.75; ) with high heterogeneity (I2 = 76%, P = 0.04). Similarly, ACEI/ARBs reduced the incidence of AF recurrence (RR = 0.39; 95%CI, 0.20-0.74; P = 0.005; ), but not new AF (RR = 0.87; 95%CI, 0.62-1.21; P = 0.40; ) with high heterogeneity (I2 = 86%, P = 0.0007), when compared to β-blockers.

Fig. 3

Forest plot of ACEI/ARBs versus β-blockers and calcium antagonists on preventing AF recurrence and new AF in long-term follow-up.

Median time of AF recurrence was reported only in 4 studies[. Du et al.[ reported that median time of AF recurrence had no significant differences between the nifedipine group and the telmisartan group. However, the other 3 studies reported that ARBs postponed AF recurrence. Therefore, preliminary comparison of these data without statistics did not reveal tendency that ACEI/ARBs could postpone AF recurrence.

Secondary endpoints

We also compared the cardiovascular events in the follow-up, which included cardiac death, myocardial infarction, stroke, and congestive heart failure. Cardiovascular events were reported in three large-scale studies[. When compared to β-blockers and calcium antagonists, ACEI/ARBs did not reduce cardiac death (RR = 1.00; 95%CI, 0.90-1.12; P = 0.94), myocardial infarction (RR = 1.00; 95%CI, 0.81-1.23; P = 0.98), and stroke (RR = 1.01; 95%CI, 0.70-1.47; P = 0.94; ). Heterogeneities were (I2 = 0%, P = 0.47), (I2 = 78%, P = 0.001), and (I2 = 94%, P<0.00001), respectively. ACEI/ARBs reduced the incidence of congestive heart failure (RR = 0.86; 95%CI, 0.77-0.96; P = 0.007; ), with low heterogeneity (I2 = 0%, P = 0.56).

Fig. 4

Forest plot of ACEI/ARBs versus control on cardiovascular events in long-term follow-up.

Data of adverse effects (bradycardia, atrial flutter, intolerable and unproductive cough, peripheral edema and dizziness) during follow-up were reported in 6 studies[. Four studies[ reported adverse effects requiring discontinuation due to bradycardia, atrial flutter, intolerable and unproductive cough, and the aggregated results of these studies suggested that ACEI/ARBs could decrease these adverse effects (RR = 0.44; 95%CI, 0.21-0.89; P = 0.02; ) with low heterogeneity (I2 = 0%, P = 0.63). In the studies of Hansson et al. (STOP-2)[ and Julius et al.[, they compared the incidence of peripheral edema and dizziness, the pooled outcomes showed that ACEI/ARBs reduced peripheral edema (RR = 0.47; 95%CI, 0.42-0.53; P<0.00001) with high heterogeneity (I2 = 57%, P = 0.13), but increased the risk of dizziness (RR = 1.11; 95%CI, 1.02-1.20; P = 0.01; ) with high heterogeneity (I2 = 51%, P = 0.15).

Fig. 5

Forest plot of ACEI/ARBs versus control on adverse effects requiring discontinuation.

Fig. 6

Forest plot of ACEI/ARBs versus control on peripheral oedema and dizziness.

Publication bias

Publication bias was assessed, even though only 10 studies were included in this analysis. The results illustrated that the probability of publication bias was possible due to asymmetry ().

Fig. 7

Funnel plot of ACEI/ARBs versus β-blockers and calcium antagonists on preventing AF recurrence and new AF in long-term follow-up.

Discussion

Regarding the effects of ACEI/ARBs on hypertensive patients and AF, the results of individual trials are conflicting. Here, we performed a meta-analysis of available data to define the conditions and circumstances in which ACEI/ARBs may be a promising preventive therapy. The pooled results from 10 RCTs using a random effects model suggested that ACEI/ARBs decreased AF recurrence rate by 7% in 3 months, and 17% in long-term follow-up. In subgroups, ACEI/ARBs reduced more AF recurrence rate by 17% than calcium antagonists and 23% than β-blockers. However, ACEI/ARBs did not decrease the rate of new AF. Compared to the control group, ACEI/ARBs did not reduce cardiac death, myocardial infarction or stroke, excepting congestive heart failure. ACEI/ARBs cut down adverse effects, but may increase dizziness.

Our meta-analysis indicated that ACEI/ARBs could decrease the incidence of AF recurrence at 3 months and in long-term follow-up. However, ACEI/ARBs could not reduce the incidence of new AF in long-term follow-up. The heterogeneities were great in subgroups analyses. We found that heterogeneities come from Hansson et al. (STOP-2)[. The blood pressures of patients in this study were higher than those in other studies, with SBP≥180 mmHg and/or DBP≥105 mmHg. Diuretics, amiloride and fixed-ratio hydrochlorothiazide were used in the β-blocker group, which may also contribute to heterogeneity. When compared to the different control groups, the incidence of AF recurrence was lower in patients receiving ACEI/ARBs than in those receiving calcium antagonists or β-blockers in long-term follow-up; however, ACEI/ARBs did not reduce new AF in long-term follow-up when compared to calcium antagonists and β-blockers. Median time to AF recurrence was described without pooled data, which did not reveal tendency that ACEI/ARBs could postpone AF recurrence.

Cardiovascular events were assessed, and the results showed that ACEI/ARBs could reduce the incidence of congestive heart failure, but not cardiac death, myocardial infarction, or stroke, comparing to β-blockers and calcium antagonists. Although ACEI/ARBs are generally regarded as safe and well tolerated drugs in most populations, it should be careful that ACEIs may induce non-productive cough and peripheral edema.

Our results are partly similar to the last 2 meta-analyses[. Huang et al.[ reported that ACEIs/ARBs were effective for new AF and AF recurrence. Han et al.[ also demonstrated that ACEI/ARBs prevented AF recurrence. In our present analysis, considering the close relation between hypertension and AF, we specifically included hypertensive patients for review. We found that ACEI/ARBs did not prevent new AF in hypertensive patients. The results are different from Huang et al.[, which may result from different included patients. In their study, patients were included as follows: myocardial infarction, coronary heart disease, hypertension and chronic heart failure, without any subgroup analysis. Furthermore, our study also investigated the role of ACEI/ARBs in cardiovascular events and adverse effects, which may provide more powerful evidence for clinicians.

Our meta-analysis has several potential limitations that should be taken into account. First, even though we analyzed calcium antagonists and β-blockers in subgroups, their characteristics are different, and the effect may be unequal. In the randomized controlled trials, the characteristics of hypertensive patients were not based on a unified level, which varies in the range of SBP≥140 mmHg and DBP≥90 mmHg. These factors may have potential impact on our results. Second, follow-up varies from 3 months to 73.2 months. Finally, as many ACEI/ARBs drugs, involving enalapril, lisinopril, ramipril, captopril, candesartan, losartan, valsartan and telmisartan, were used in our included studies, and we are not sure to assess the impact of ACEI/ARBs basing on meaningful endpoints.

In conclusion, our results suggest that ACEI/ARBs may reduce the incidence of AF recurrence, heart failure, with less serious adverse effects. Further unified protocol and well-designed randomized controlled trials on this topic are still needed.