A randomized controlled trial of eplerenone in asymptomatic phospholamban p.Arg14del carriers

Abstract

Phospholamban (PLN; p.Arg14del) cardiomyopathy is an inherited disease caused by the pathogenic p.Arg14del variant in the PLN gene. Clinically, it is characterized by malignant ventricular arrhythmias and progressive heart failure.1,2 Cardiac fibrotic tissue remodelling occurs early on in PLN p.Arg14del carriers.3,4 Eplerenone was deemed a treatment candidate because of its beneficial effects on ventricular remodelling and antifibrotic properties.5,6 We conducted the multicentre randomized trial ‘intervention in PHOspholamban RElated CArdiomyopathy STudy’ (i-PHORECAST) to assess whether treatment with eplerenone of asymptomatic PLN p.Arg14del carriers attenuates disease onset and progression. The i-PHORECAST was a clinical trial following the prospective, randomized, open, blinded endpoint design7 and registered in the clinicaltrials.gov-register (registration number: NCT01857856). The i-PHORECAST design manuscript has been published previously.8 Carriers without symptoms were selected from the national PHOspholamban RElated CArdiomyopathy STudy (PHORECAST) registry (https://www.phorecast.nl/), which collected all PLN p.Arg14del carriers known at the time of study inception (n = 436). At an initial screening visit, asymptomatic status was verified. Study participants were 18 to 65 years of age, genotype-confirmed PLN p.Arg14del carriers, and asymptomatic: no cardiac symptoms, New York Heart Association class I, a left ventricular ejection fraction (EF) measured with cardiac magnetic resonance imaging (CMR) of ≥ 45%, no diagnosis of dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy, no treatment with cardioactive medication at inclusion, no history of (non-)sustained ventricular tachycardia or fibrillation, ≤2500 premature ventricular contractions (PVCs) during 24-h Holter monitoring, no evidence of ischaemic heart disease, and no history of hyperkalaemia, severe renal dysfunction, or hepatic impairment. Additionally, pregnant women, women pregnant during the 60 days before potential inclusion, and women planning on becoming pregnant were excluded from the trial. Study participants were randomized 1:1 to receive either 50 mg of eplerenone once daily or no treatment. The follow-up duration was 3 years. Twelve-lead electrocardiogram (ECG), 24-h three-channel Holter registration, exercise testing, physical examination, medical history and event review, and venous blood analysis were performed yearly and assessed by experienced cardiologists. Cardiac magnetic resonance imaging was performed at baseline and at the end of follow-up (3 years). The composite primary endpoint consisted of: a ≥10% increase in left and/or right ventricular end-diastolic volume (L/RVEDV), a ≥5% decrease in left and/or right ventricular EF (L/RVEF), new development of late gadolinium enhancement (LGE) as a measure of cardiac fibrosis, a ≥100% increase and absolute increase of ≥1000 PVCs on Holter registration, development of non-sustained ventricular tachycardia, a decrease in QRS voltage on ECG of ≥25%, development of cardiac symptoms necessitating treatment, and cardiovascular death. New development of LGE was defined as LGE observed in participants whose initial CMR did not contain LGE. A blinded committee adjudicated the endpoints. Continuous data are given as medians (interquartile range; IQR). Categorical values are given as absolute values (%). All percentages provided are calculated using a cohort size of n = 84 and a group size of n = 42 unless stated otherwise. Dichotomous variables were compared using the χ2 test. Continuous variables were compared using the Kruskal–Wallis test. Sample size estimation was based on the prediction that 50% of asymptomatic PLN p.Arg14del carriers would reach the primary endpoint within 3 years and a predicted treatment effect of eplerenone of 50%. To ensure 80% power at a 0.05 significance level with an assumed 15% loss to follow-up during the study, a required cohort size of 150 study participants (75 in each group) was estimated. From May 2014 until January 2018, 84 carriers from the initial selection of 436 p.Arg14del PLN carriers were enrolled, which was markedly lower than the target number of participants (150), resulting in an underpowered sample size. In total, paired CMR data of sufficient quality was available of 74 out of 84 carriers, 37 in both the eplerenone group and the control group. Characteristics of the total cohort at baseline and at end of study are listed in Table 1. There were no statistically significant differences between the groups. Baseline and end of study characteristics, endpoint distribution All percentages are calculated using a total cohort size of 84 and a group size of 42. PVCs, premature ventricular contractions. Baseline and end of study characteristics, endpoint distribution All percentages are calculated using a total cohort size of 84 and a group size of 42. PVCs, premature ventricular contractions. Median age at inclusion was 39 years (Q1–Q3: 27–50 years), 37 (44%) people were male. After 3 years follow-up, 56/84 (67%) people showed evidence of disease progression by reaching the composite endpoint, 29/42 (69%) in the control group and 27/42 (64%) in the eplerenone group (P = 0.817). The two components of the primary endpoint that were most often reached were a decrease in left ventricular EF (29/84, 35%) and/or right ventricular EF by ≥5% (24/84, 29%), followed by the combination of non-sustained ventricular tachycardia and increase in PVC count on Holter monitoring (14/84, 17%). In total, 14/84 (17%) people already showed some LGE at baseline despite their asymptomatic status, 9/42 (21%) in the eplerenone group and 5/42 (12%) in the control group (P = 0.520). Out of 10 carriers with newly observed LGE at the end of the study, a decrease in ventricular function or an increase in ventricular volume was observed in five. No sustained ventricular tachycardia was observed during the trial. Sporadic QRS amplitude decrease was observed, but no newly developed low voltage ECGs were observed. Eplerenone was well-tolerated with no significant difference in the occurrence of adverse events between the groups. Within the 3-year duration of i-PHORECAST trial, disease progression, i.e. reaching the composite endpoint, was observed in two-thirds of participants, both in members of the eplerenone and control groups. Moreover, signs of PLN p.Arg14del cardiomyopathy were already present at baseline, in particular LGE, despite the asymptomatic status of participants. These findings provide a novel perspective regarding PLN p.Arg14del cardiomyopathy. Given the fact that the sample size was smaller than expected, conclusions from this study must be drawn with caution, particularly regarding the effect of eplerenone. Although no signal for such an effect was observed, we cannot exclude that with the intended sample size this might have been observed. There was no evidence of an effect of treatment with eplerenone based on this analysis. Eplerenone itself was safe and well-tolerated. Future research into PLN p.Arg14del cardiomyopathy disease progression or modification—and more broadly, research into asymptomatic carriers of pathogenic variations associated with genetic cardiomyopathies—may be better designed using the knowledge obtained in this study. The authors would like to thank cardiologists A.J. Perez-Matos and P.L. van Haelst from the St. Antonius medical centre in Sneek, the Netherlands for their assistance in acquiring necessary study data. The data underlying this article cannot be shared publicly due to concerns regarding the privacy of individuals who participated in the study. The data, or a subset thereof, will be shared on reasonable request to the corresponding author. This work was financially supported by the Netherlands Cardiovascular Research Initiative, an initiative supported by the Dutch Heart Foundation (The Hague, Netherlands): PREDICT 1 (CVON2012-10) and 2 (CVON 2018-30), DOSIS (CVON 2014-40) and eDETECT (CVON 2015-30). Furthermore, this study was supported by a grant (836011002) from ZonMW and the Leducq Foundation (CURE-PLaN). Eplerenone was provided by Pfizer. W.P.t.R. is supported by the Dutch Heart Foundation (Young Talent Program CVON PREDICT) and the Leducq Foundation (Postdoctoral Fellowship CURE-PLaN; Netherlands Heart Institute). B.D.W is supported by the Netherlands Organisation for Scientific Research (NWO VENI grant 016.176.147) and the Netherlands Heart Foundation Senior Clinical Scientist Grant (2019T064). P.vd.M. is supported by a grant from the European research Council (ERC CoG 101045236, DISSECT-HF) H.L.T. has received funding from the European Union's Horizon 2020 research and innovation programme under acronym ESCAPE-NET, registered under grant agreement No 733381. F.W.A. is supported by UCL Hospitals NIHR Biomedical Research Centre. R.A.d.B. is supported by a grant from the European Research Council (ERC CoG 818715, SECRETE-HF).

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