Open Access
01.02.2020 | Original Research Article
Effect of Spironolactone on Atrial Fibrillation in Patients with Heart Failure with Preserved Ejection Fraction: Post-Hoc Analysis of the Randomized, Placebo-Controlled TOPCAT Trial
verfasst von:
Jolien Neefs, Nicoline W. E. van den Berg, Sébastien P. J. Krul, S. Matthijs Boekholdt, Joris R. de Groot
Mineralocorticoid receptor antagonists (MRAs) reduce the risk of atrial fibrillation (AF) in patients with heart failure (HF) and a reduced ejection fraction. The efficacy of MRAs for AF prevention in patients with HF and a preserved ejection fraction (HFpEF) is unclear.
Objectives
We performed a secondary analysis of a randomized placebo-controlled trial to determine the efficacy of spironolactone in reducing new-onset AF and recurrence of AF in 2733 patients with symptomatic HFpEF.
Methods
Patients with and without prevalent AF at baseline were included, and those with permanent AF were excluded. Patients were randomized 1:1 to spironolactone or placebo. The risk of new-onset AF or the recurrence of AF was quantified using hazard ratios (HRs) with corresponding 95% confidence intervals (CIs).
Results
At baseline, 2228 (64.7%) patients had no history of AF (spironolactone, n = 1111; placebo, n = 1117), whereas 505 (18.4%) patients had prevalent AF (spironolactone, n = 260; placebo, n = 245). During a median follow-up of 3.1 years (interquartile range [IQR] 2.0–4.9), the incidence of new-onset AF was similar in both treatment arms: spironolactone 5.2% (n = 58) versus placebo 4.4% (n = 49); p = 0.41. The risk of new-onset AF was similar in both treatment arms: HR 1.19; 95% CI 0.81–1.74; p = 0.38. AF recurrence was also similar in both treatment arms during a median follow-up of 3.3 years (IQR 1.9–4.7): spironolactone 11.5% (n = 30) versus placebo 11.8% (n = 29); p = 1.00. The risk of recurrence of AF did not differ per treatment arm: HR 0.94; 95% CI 0.57–1.58; p = 0.83.
Conclusion
Spironolactone does not reduce the risk of new-onset AF or AF recurrence in patients with HFpEF. This is in contrast to results in cohorts of patients with HF and a reduced ejection fraction.
Atrial fibrillation (AF) is a common comorbidity in patients with symptomatic heart failure with a preserved ejection fraction.
Spironolactone treatment did not reduce the risk of new-onset AF or recurrence of AF in patients with heart failure and a preserved ejection fraction.
Specifically, in patients with comorbidities related to an increased risk of AF, such as hypertension and obesity, spironolactone did not reduce new-onset AF or recurrence of AF.
These findings are in contrast to previous findings in patients with symptomatic heart failure with a reduced ejection fraction.
1 Introduction
Heart failure (HF) is a recognized risk factor for new-onset atrial fibrillation (AF) and recurrence of AF [1]. Moreover, AF is the most common arrhythmia in HF independent of left ventricle ejection fraction (LVEF) [2]. The increased risk of AF in patients with HF can be partly explained by enhanced activation of the renin-angiotensin-aldosterone system (RAAS) and subsequent aldosterone production [1, 3].
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Aldosterone competitively binds to the mineralocorticoid receptor, initiating—among other effects—structural cardiac remodeling, a process driven by fibrosis formation [4, 5]. Like HF, AF is characterized by structural atrial remodeling due to atrial fibrosis [6]. Consequently, aldosterone pathway blockade by mineralocorticoid receptor antagonists (MRAs), such as spironolactone and eplerenone, may reduce HF symptoms and the risk of AF. MRAs were found to be effective in reducing new-onset AF or recurrence of pre-existent AF in patients with HF, not further specified [7]. Moreover, a secondary analysis of the EMPHASIS-HF (Eplerenone in Mild Patients Hospitalization And SurvIval Study in Heart Failure) trial, which included only patients with HF with a reduced ejection fraction (HFrEF), showed that eplerenone significantly reduced new-onset AF [8, 9].
A post-hoc analysis of the TOPCAT (Treatment of Cardiac Function with an Aldosterone Antagonist; NCT00094302) trial assessed the influence of AF at baseline on HF outcomes. Patients with AF had a higher cardiovascular risk than patients without AF, independent of spironolactone use [10]. However, whether spironolactone has a beneficial effect on the prevention of new-onset AF or recurrence of AF in patients with HF and a preserved ejection fraction (HFpEF) is currently unknown. The primary objective of this analysis was to determine the efficacy of spironolactone in patients with HFpEF included in the TOPCAT study in reducing new-onset AF (i.e., AF in patients without a previous history of AF) and recurrence of AF (i.e., AF in patients with AF at baseline or patients in sinus rhythm, but with a medical history of AF), separately. Second, the efficacy of spironolactone was determined in subgroups defined by previously recognized AF risk factors.
2 Methods
TOPCAT was a phase III, multicenter, international, randomized, double-blind, placebo-controlled trial. A detailed description of the study design and data collection has been previously published [11, 12]. The trial was approved by each study site ethics committee, and all patients provided written consent before inclusion. In brief, the trial was designed to determine whether spironolactone treatment in patients with HFpEF improved the composite endpoint of death from cardiovascular causes, aborted cardiac arrest or hospitalization for the management of HF. We included all patients in the TOPCAT study in the current analysis and performed subanalysis on the region of inclusion, as this has been suggested to have affected the results of the main study [13].
2.1 Study Design
Patients were eligible when diagnosed with symptomatic HF and LVEF ≥ 45% combined with either a hospitalization for HF within 12 months prior to inclusion or an elevated natriuretic peptide level (brain natriuretic peptide [BNP] ≥ 100 pg/mL or N-terminal pro-BNP [NT-proBNP] ≥ 360 pg/mL) within 60 days prior to inclusion. Patients had to be aged ≥ 50 years, have controlled systolic blood pressure < 140 mmHg (or ≤ 160 mmHg if the patient was taking three or more medications to control blood pressure), and a serum potassium level < 5.0 mmol/L. The main exclusion criteria were life expectancy < 3 years, estimated glomerular filtration rate (eGFR) < 30 ml/min/1.73 m2 body surface area or serum creatinine ≥ 2.5 mg/dL. Inclusion and exclusion criteria were described in detail in the main study publication [11, 12].
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Initially, the TOPCAT investigators determined a positive history of AF from patients’ medical charts and baseline electrocardiogram (ECG). This was reported in study case report forms (CRFs). The presence of AF for the current analysis was obtained from the CRFs, which were made available to the investigators by the National Heart, Lung and Blood Institute’s Biologic Specimen and Data Repository Information Coordinating Center. For the current analysis, patients with permanent AF were excluded.
Patients were randomized 1:1 to receive spironolactone or placebo. Initial dosage of study drugs was 15 mg once daily, increased to a maximum of 45 mg daily during the first 4 months after randomization, if tolerated and adjusted, if required.
2.2 Atrial Fibrillation (AF) Ascertainment
AF was a predetermined secondary outcome of the TOPCAT trial. Patients were followed for a minimum of 15 months to assess primary and secondary outcomes of the TOPCAT trial. During scheduled outpatient clinic visits, AF occurrence was evaluated or obtained from patient medical charts and reported in the CRFs. New-onset AF or recurrence of AF during follow-up was obtained from the CRF specifically designed for registration of AF occurrence [12]. All ECGs or rhythm strips of cases of new-onset or recurrent AF were adjudicated by a critical event committee.
2.3 Statistical Analysis
Baseline characteristics of patients with and without AF at baseline were compared using unpaired sample t tests for continuous variables and using Pearson’s χ2 for categorical variables. The primary outcome of the current analysis was the onset of AF or recurrence of prevalent AF. Kaplan–Meier estimates were used to compute the cumulative incidence of AF, and log-rank was used for between-group comparisons. Cox proportional hazards models were used to quantify the risk of new-onset or recurrent AF, and expressed as hazard ratios (HRs) with corresponding 95% confidence intervals (CIs). Patients who did not have an episode of AF were censored at the date of last available follow-up information. Incidence rates per 1000 person-years were calculated.
Furthermore, the influence of AF at baseline on HF symptoms was determined by assessing the risk of the primary outcome of the TOPCAT trial (composite of death from cardiovascular causes, aborted cardiac arrest or hospitalization for the management of HF) stratified for a history of AF at baseline using Cox proportional hazards models.
To assess the homogeneity of the drug effect, prespecified subgroups from the initial TOPCAT trial were used in Cox proportional hazards models [11].
To assess potential regional differences, sensitivity analyses were conducted using Cox proportional hazards models [13, 14]. Further sensitivity analyses were conducted to assess the influence of concomitant angiotensin-converting-enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs).
Data were analyzed using SPSS version 24 (IBM, Armonk, NY, USA) and R 3.3.2. A two-sided p value of < 0.05 was considered to be significant.
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3 Results
3.1 Study Population
A total of 3445 patients were included in the TOPCAT trial. At baseline, 2228 patients (64.7%) had no history of AF (spironolactone, n = 1111; placebo, n = 1117), and prevalent AF was present in 505 (14.7%) patients (spironolactone, n = 260; placebo, n = 245) (Table 1). In total, 672 (19.5%) patients had permanent AF so were excluded from the current analysis. Baseline characteristics of patients without a history of AF at baseline were equally distributed between both treatment arms. This also applied to patients with prevalent AF. Beta-blockers, ACE inhibitors and ARBs were extensively prescribed in the TOPCAT trial but similarly in both treatment arms for patients with and without AF at baseline. There were significant, but clinically moderately relevant, differences in baseline characteristics between patients with prevalent AF and those without AF. Patients with prevalent AF were older but had lower rates of diabetes mellitus and coronary artery disease. Patients with prevalent AF at baseline were more frequently eligible for inclusion in the TOPCAT trial because of elevated natriuretic peptides than because of hospitalization for HF. Patients with prevalent AF at baseline had a significant larger left atrial volume index than patients without a history of AF at baseline (albeit, on average, lower than the upper boundary of normal). Most patients with prevalent AF showed sinus rhythm on their baseline ECG (spironolactone 84.6% vs. placebo 81.2 %; p = 0.06). At baseline, AF was significantly more reported in patients from Russia and Georgia than in patients from the Americas (18.9 vs. 15.5%, respectively; p = 0.047).
Table 1
Baseline characteristics of 2733 patients with and without prevalent atrial fibrillation
Characteristics
Prevalent AF at baseline
No AF at baseline
p Valuea
Spironolactone (n = 260)
Placebo (n = 245)
Total (n = 505)
Spironolactone (n = 1111)
Placebo (n = 1117)
Total (n = 2228)
Age, years
71 (63–79)
71 (64–79)
71 (64–79)
67 (60–74)
67 (59–74)
67 (60–74)
< 0.001
Females
131 (50.4)
130 (53.1)
261 (51.7)
613 (55.2)
601 (53.8)
1214 (54.5)
0.28
White race
242 (93.1)
227 (92.7)
469 (92.9)
964 (86.8)
981 (87.8)
1945 (87.3)
< 0.001
LVEF, %
61 (56–64)
59 (52–65)
60 (54–64)
60 (56–64)
61 (56–65)
61 (56–65)
< 0.001
LAVI, mL/m2
29 (22–39)
30 (22–35)
29 (22–37)
24 (19–31)
25 (20–31)
25 (19–31)
< 0.001
NYHA class
0.09
I–II
172 (66.2)
163 (66.5)
335 (66.3)
777 (69.9)
791 (70.8)
1568 (70.4)
III–IV
88 (33.8)
81 (33.1)
169 (33.5)
333 (30.0)
324 (29.0)
657 (29.5)
Heart rate, beats/min
66 (60–73)
66 (60–74)
66 (60–73)
68 (61–75)
68 (61–75)
68 (61–75)
< 0.001
Blood pressure, mmHg
Systolic
129 (120–135)
130 (120–137)
130 (120–136)
130 (120–140)
130 (120–140)
130 (120–140)
< 0.001
Diastolic
76 (66–80)
76 (70–80)
76 (68–80)
80 (70–83)
80 (70–84)
80 (70–84)
< 0.001
BMI, kg/m2
31 (27–36)
30 (27–35)
31 (27–36)
31 (27–35)
31 (27–36)
31 (27–36)
<0.001
CADb
139 (53.5)
154 (62.9)
293 (58.0)
685 (61.7)
713 (63.8)
1398 (62.7)
0.05
Hypertension
240 (92.3)
222 (90.6)
462 (91.5)
1010 (90.9)
1038 (92.9)
2048 (91.9)
0.82
Diabetes mellitus
73 (28.1)
57 (23.3)
130 (25.7)
375 (33.8)
384 (34.4)
759 (34.1)
< 0.001
Eligibility stratum
< 0.001
Hospitalization in previous year; HF management a major component
172 (66.2)
170 (69.4)
342 (67.7)
846 (76.1)
831 (74.4)
1677 (75.3)
Elevated NPs in previous 60 days
88 (33.8)
75 (30.6)
163 (32.3)
265 (23.9)
286 (25.6)
551 (24.7)
Region of enrollment
< 0.001
Americasc
152 (58.5)
128 (52.2)
280 (55.4)
511 (46.0)
511 (45.7)
1022 (45.9)
Russia and Georgia
108 (41.5)
117 (47.8)
225 (44.5)
600 (54.0)
606 (54.3)
1206 (54.1)
Serum BNP, pg/mL
276 (157–542)
267 (148–563)
272 (149–546)
206 (135–487)
224 (128–398)
220 (131–426)
< 0.001
Serum NT-proBNP, pg/mL
784 (503–1634)
710 (441–2034)
784 (480–1877)
604 (382–1165)
698 (408–1625)
647 (387–1362)
< 0.001
Serum potassium, mmol/L
4.3 (4.0–4.6)
4.3 (4.0–4.6)
4.3 (4.0–4.6)
4.3 (4.0–4.6)
4.3 (4.0–4.6)
4.3 (4.0–4.6)
< 0.001
Serum creatinine, mg/dL
1.1 (0.9–1.3)
1.1 (0.9–1.2)
1.1 (0.9–1.3)
1.0 (0.9–1.2)
1.0 (0.9–1.2)
1.0 (0.9–1.2)
< 0.001
eGFR, mL/min/1.73 m2
61.9 (50.9–76.3)
64.0 (53.0–77.9)
63.1 (52.0–76.9)
67.4 (56.1–81.1)
66.2 (54.6–80.3)
66.9 (55.3–80.6)
< 0.001
Serum hemoglobin, g/dl
13.2 (11.9–14.2)
13.2 (12.4–14.5)
13.2 (12.0–14.3)
13.1 (12.1–14.2)
13.2 (12.1–14.3)
13.1 (12.1–14.3)
< 0.001
Medications
ACE inhibitor
152 (58.5)
149 (60.8)
301 (59.6)
755 (68.0)
760 (68.0)
1515 (68.0)
< 0.001
ARB
60 (23.1)
49 (20.0)
109 (21.6)
212 (19.1)
207 (18.5)
419 (18.8)
0.17
Aspirin
155 (59.6)
146 (59.6)
301 (59.6)
805 (72.5)
829 (74.2)
1634 (73.4)
< 0.001
β-blocker
183 (70.4)
169 (69.0)
352 (69.7)
881 (79.3)
868 (77.7)
1749 (78.5)
< 0.001
CCB
94 (36.2)
86 (35.1)
180 (35.6)
418 (37.6)
465 (41.6)
883 (39.6)
0.11
Diuretic
218 (83.8)
205 (83.7)
423 (83.8)
866 (77.9)
885 (79.2)
1751 (78.6)
0.01
Long-acting nitrate
37 (14.2)
36 (14.7)
73 (14.5)
180 (16.2)
175 (15.7)
355 (15.0)
0.45
Statin
146 (56.2)
140 (57.1)
286 (56.6)
584 (52.6)
572 (51.2)
1156 (51.9)
0.06
Warfarin
119 (45.8)
108 (44.1)
227 (45.0)
59 (5.3)
40 (3.6)
99 (4.4)
< 0.001
Data are presented as n (%) or (IQR) unless otherwise indicated. Ultrasound data were available in 935 patients
ACE angiotensin-converting-enzyme, AF atrial fibrillation, ARB angiotensin II receptor blocker, BMI body mass index, BNP brain natriuretic peptide, CAD coronary artery disease, CCB calcium channel blocker, eGFR estimated glomerular filtration rate, HF heart failure, LAVI left atrial volume index, LVEF left ventricular ejection fraction, NT-proBNP N-terminal pro-BNP, NYHA New York Heart Association
aNo AF versus prevalent AF
bCAD includes myocardial infarction, coronary artery bypass graft, percutaneous intervention or angina pectoris
cThe Americas included the USA, Canada, Argentina and Brazil
After stratification based on history of AF at baseline, spironolactone did not reduce the risk of the primary composite outcome of death from cardiovascular causes, aborted cardiac arrest or hospitalization for the management of HF in patients either with or without a history of AF at baseline (Figs. 1 and 2 in the Electronic Supplementary Material [ESM]).
3.2 New-Onset AF During Follow-Up
During a median follow-up of 3.1 years (interquartile range [IQR] 2.0–4.9), new-onset AF occurred in 5.2% (n = 58) of those treated with spironolactone compared with 4.4% (n = 49) of those treated with placebo (p = 0.41) (Fig. 1). This yielded an event rate of 15.8 per 1000 person-years for spironolactone and 13.3 for placebo. The event rate, but not the differential efficacy of spironolactone versus placebo, significantly differed by region of inclusion (Americas 7.4% vs. Russia and Georgia 3.1%; p < 0.001). The risk of new-onset AF was not significantly different between spironolactone and placebo (HR 1.19; 95% CI 0.81–1.74; p = 0.38 with log-rank test) (Fig. 2).
Fig. 1
Cumulative hazard ratio (%) of a new-onset atrial fibrillation (AF) and b recurrence of AF for spironolactone versus placebo
Fig. 2
Number of patients with new-onset AF or recurrence of AF during follow-up for spironolactone versus placebo. AF atrial fibrillation, CI confidence interval, HR hazard ratio
×
×
Furthermore, subgroup analyses according to subgroups prespecified in the main TOPCAT publication did not reveal any significant study drug effect on new-onset AF (Fig. 3 in the ESM). Importantly, sensitivity analysis based on region of inclusion demonstrated no differences between the regions (Americas, HR 1.02; 95% CI 0.64–1.64, p = 0.92; Russia and Georgia, HR 1.53; 95% CI 0.78–3.01, p = 0.22) (Fig. 3). Concomitant use of ACE inhibitors, ARBs did not alter the results, nor did concomitant use of any β-blocker (data not shown).
Fig. 3
Forest plot of the hazard ratios of new-onset AF or recurrence of AF stratified for region of inclusion. The Americas included the USA, Canada, Argentina and Brazil. AF atrial fibrillation, CI confidence interval, HR hazard ratio, p p value
×
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3.3 Recurrence of AF During Follow-Up
During a median follow-up of 3.3 years (IQR 1.9–4.7), AF recurred in 11.5% (n = 30) of patients with a history of prevalent AF treated with spironolactone compared with 11.8% (n = 29) of those treated with placebo (p = 1.00) (Fig. 1). This yielded an event rate of 35.4 per 1000 person-years for spironolactone and 37.1 for placebo. The rate of AF recurrence was similar per region of inclusion: Americas, 11.6%; Russia and Georgia, 15.4%; p = 0.37. The risk of AF recurrence did not differ between spironolactone- and placebo-treated patients: HR 0.94; 95% CI 0.57–1.58; p = 0.83 with log-rank test (Fig. 2).
Furthermore, subgroup analyses according to subgroups prespecified in the main TOPCAT publication did not reveal any significant study drug effect on recurrence of AF (Fig. 4 in the ESM). Importantly, sensitivity analysis based on region of inclusion demonstrated no differences between the regions: Americas, HR 0.89; 95% CI 0.43–1.85; p = 0.76; Russia and Georgia, HR 0.97; 95% CI 0.47–2.01; p = 0.93 (Fig. 3). Concomitant use of ACE inhibitors or ARBs did not alter the results, nor did concomitant use of any β-blocker (data not shown).
4 Discussion
The current secondary analysis of the TOPCAT trial assessed the efficacy of MRAs on the risk of new-onset AF or recurrence of AF separately in patients with HFpEF in a large, randomized, double-blind, placebo-controlled trial. Spironolactone did not reduce new-onset AF or recurrence of AF compared with placebo in patients with symptomatic HFpEF. Moreover, subgroup analyses did not reveal any significant differences. Specifically, in patients with comorbidities related to an increased risk of AF, such as an enlarged left atrium, hypertension and obesity, spironolactone did not reduce new-onset AF or recurrence of AF. These findings are in contrast to prior findings in patients with HRrEF. In a secondary analysis of the EMPHASIS-HF trial, eplerenone reduced new-onset AF by 42% compared with placebo [9]. However, we show that spironolactone does not prevent new-onset or recurrent AF in patients with HFpEF, irrespective of region of inclusion or sex. These contradicting results may be explained by either patient- or substrate-related differences.
First, patients with HFrEF tend to have prevalent coronary artery disease, whereas patients with HFpEF have an underlying risk profile comprising a combination of known cardiac risk factors [2]. Patients from the TOPCAT trial reflect the characteristics of patients with HFpEF as described in the literature, with a very high prevalence of hypertension [15]. Moreover, the incidence of AF differs between HFrEF and HFpEF, in that AF is more common in patients with HFpEF than in those with HFrEF [16]. The current analysis found a relatively low incidence of new-onset AF. However, after comparison of the region of inclusion, event rates in the Americas conformed to those described in the literature, which we discuss later in this article.
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Second, the absence of reduction of AF incidence by MRAs in HFpEF may be explained by the distinctive underlying process of cardiovascular remodeling. For example, HFrEF has been associated with degradation and focal fibrosis formation, whereas fibrosis formation in HFpEF is less obvious [17]. Therefore, other processes may prevail in the AF substrate in patients with HFpEF. Importantly, HFpEF is characterized by increased left atrial stiffness and pressure overload, which is thought to contribute to the high burden of AF in patients with HFpEF [18], which MRAs may not particularly affect. Furthermore, it has been suggested that cardiac remodeling in HFpEF can be attributed to systemic inflammation. This, in turn, may lead to both cardiac and noncardiac comorbidities, involving myocardial microvascular dysfunction, leading to myocardial remodeling and dysfunction [17, 19]. Although not tested in the current analysis, these processes may have contributed to the arrhythmogenic substrate in subjects participating in the TOPCAT trial.
Third, it can be rationalized that a decrease of AF onset or recurrence in patients with HFrEF may be the result of a decrease in HF outcomes. The lack of an effect of spironolactone on the prevention of new-onset AF or AF recurrence in this study may be due to the neutral primary results concerning HF outcomes in the TOPCAT trial. Indeed, TOPCAT investigators stratified patients to AF or no AF at baseline and found no differential effect of spironolactone or placebo on the main study outcomes [10]. This may imply that the effect of MRAs on AF occurrence is dependent on HF symptoms. However, Dabrowski et al. [20] randomized patients with paroxysmal AF without HF and with a mean ejection fraction of 69% to spironolactone or no spironolactone. Recurrence of AF was significantly less frequent in patients treated with spironolactone. Importantly, systolic and diastolic blood pressure did not differ between treatment arms [20]. Thus, although an indirect effect of spironolactone on AF via the treatment of HF may well be possible, an additional effect on the AF substrate (i.e., fibrosis formation) seems likely. Interestingly, the RAAS activity has been suggested to play a larger role in HFrEF than in HFpEF [21, 22]. Combining these factors, it is likely that MRAs alter the risk of AF by reducing profibrotic pathways in the atrial wall, which are triggered by RAAS activation and aldosterone production in the setting of HFrEF. Indeed, the concentration of plasma markers of cardiac fibrosis (carboxy- and amino-terminal propeptide of procollagen type-I [PICP and PINP] and type-III [PIIINP]) decreased after administration of MRA in patients with HFrEF [23]. However, a meta-analysis also found a reduction of cardiac fibrosis markers in patients with HFpEF who were administered MRAs [24].
4.1 Limitations
Some aspects of our study should be considered when interpreting the results of this secondary analysis. The presence of AF was derived from the specified case study forms, which may have led to incorrect categorization of AF type. It is therefore also possible that the true incidence of AF was underestimated. In particular, events tended to be underreported in patients from Russia and Georgia, as also described for the primary outcome of the TOPCAT trial [11]. However, we cannot exclude the possibility that the AF cases identified and reported in the CRFs were those demanding physician contact. Therefore, it can be argued that the clinically most relevant AF episodes are those that are symptomatic and demand physician contact; this limitation pertains to both randomized treatment arms. Further, the TOPCAT investigators reported a significantly lower systolic blood pressure in the spironolactone group during follow-up (mean decrease of 2.2 vs. 0.2 mmHg for spironolactone and placebo, respectively; p < 0.001) [11]. AF episodes may have been more symptomatic in patients with low blood pressure, but the mean decrease in systolic blood pressure was relatively mild.
Lastly, the trial included patients drawn from two different regions, the Americas and Russia plus Georgia. These regions included patients with different baseline characteristics. In a secondary analysis, the TOPCAT investigators showed a disparate effect of spironolactone. In patients from the Americas, spironolactone significantly reduced the risk of the primary outcome, but this effect was not significant in patients from Russia and Georgia [13]. In patients randomized to spironolactone, the serum level of canrenone (the active metabolite of spironolactone) was significantly more frequently undetectable in patients from Russia and Georgia than in those from the Americas. The investigators concluded that the study results from Russia and Georgia did not reflect the true therapeutic effect of spironolactone [14]. The current analyses were all based on an intent-to-treat population. However, our sensitivity analysis focusing on region of inclusion did not demonstrate different results with respect to new-onset AF or AF recurrence between both regions. This argues for the inclusion of the patients from Russia and Georgia in the current analysis.
5 Conclusion
Spironolactone does not decrease the risk of new-onset AF or recurrence of AF in patients in the TOPCAT study diagnosed with symptomatic HFpEF. Our findings contrast with previous findings in patients with HFrEF. Further effort is needed to find an effective treatment to reduce the risk of AF, since AF episodes are related to increased hospitalization, stroke and mortality rates.
Acknowledgements
The authors thank the TOPCAT investigators. This manuscript was prepared using TOPCAT Research Materials obtained from the National Heart, Lung, and Blood Institute (NHLBI) Biologic Specimen and Data Repository Information Coordinating Center and does not necessarily reflect the opinions or views of the TOPCAT study organization or the NHLBI.
Compliance with Ethical Standards
Funding
No sources of funding were used to conduct this study or prepare this manuscript.
Conflicts of Interest
Dr. de Groot is a consultant for AtriCure and Daichii Sankyo; has received research grants from AtriCure, Medtronic, Boston Scientific and Abbott and a grant from ZonMW/now (106.146.310) outside the submitted work. Jolien Neefs, Nicoline van den Berg, Sébastien Krul and S. Matthijs Boekholdt have no potential conflicts of interest that might be relevant to this work.
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Effect of Spironolactone on Atrial Fibrillation in Patients with Heart Failure with Preserved Ejection Fraction: Post-Hoc Analysis of the Randomized, Placebo-Controlled TOPCAT Trial
verfasst von
Jolien Neefs Nicoline W. E. van den Berg Sébastien P. J. Krul S. Matthijs Boekholdt Joris R. de Groot
Routinemäßige Mammografien helfen, Brustkrebs frühzeitig zu erkennen. Anhand der Röntgenuntersuchung lassen sich aber auch kardiovaskuläre Risikopatientinnen identifizieren. Als zuverlässiger Anhaltspunkt gilt die Verkalkung der Brustarterien.
Wenn unter einer medikamentösen Hochdrucktherapie der diastolische Blutdruck in den Keller geht, steigt das Risiko für schwere kardiovaskuläre Ereignisse: Darauf deutet eine Sekundäranalyse der SPRINT-Studie hin.
Beginnen ältere Männer im Pflegeheim eine Antihypertensiva-Therapie, dann ist die Frakturrate in den folgenden 30 Tagen mehr als verdoppelt. Besonders häufig stürzen Demenzkranke und Männer, die erstmals Blutdrucksenker nehmen. Dafür spricht eine Analyse unter US-Veteranen.
Der als Antidiabetikum sowie zum Gewichtsmanagement zugelassene Wirkstoff Tirzepatid hat in Studien bei adipösen Patienten auch schlafbezogene Atmungsstörungen deutlich reduziert, informiert der Hersteller in einer Vorab-Meldung zum Studienausgang.
Update Kardiologie
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