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Cardiology Research

Review

Volume 11, Number 4, August 2020, pages 213-218

Upstream Therapy for Atrial Fibrillation Prevention: The Role of Sacubitril/Valsartan

In recent years, considering the uninspiring results of classic antiarrhythmic drugs, other not strictly antiarrhythmic drugs have been taken into account for the treatment of AF, with the aim of correcting the substrate underlying the arrhythmia and to modify its evolution (upstream treatment), thus preventing both the first episode of AF (primary prevention) and relapses (secondary prevention). It is known that AF in itself determines electrical modifications [1, 2] and structural changes of the atria [1-4] represented essentially by a shortening and dispersion of the action potential, atrial enlargement and fibrosis (so called remodeling), which then make the restoration of the sinus rhythm and its subsequent maintenance more problematic. The upstream treatment aims to counter and/or delay this remodeling process by acting at different levels and with different mechanisms, such as the blockade of the renin-angiotensin-aldosterone system, the antifibrotic and anti-inflammatory effect, the reduction of oxidative stress, etc.

According to the most credited thesis, the drugs that can be used for upstream prevention of AF would prevent AF through an improvement of systemic and pulmonary hemodynamics, as in the case of angiotensin-converting enzyme inhibitors (ACEIs) and sartans, or through a pleiotropic effect of prevention of atrial fibrosis, such as in the case of statins, or through a reduction in oxidative stress, as postulated for omega-3 fatty acids.

Information is provided below regarding the upstream treatment of AF with each of these drug classes.

Atrial stretch and inflammation have been shown to increase the level of angiotensin II in the heart. Angiotensin II in turn causes calcium overload and atrial fibrosis, two essential conditions for electrophysiological changes (shortening of refractoriness and slowing of conduction), which favor the initiation and maintenance of AF. Some experimental studies have shown that both ACEIs [5] and ARBs [6, 7] are able to prevent the electrical and mechanical remodeling that is observed in AF.

Overall the published data, even if mainly consisting of post hoc analyses of studies with endpoints different from the occurrence of AF, seem to support the role of ACEIs and ARBs in primary AF prevention, at least in patients with heart failure [8]. Regarding secondary AF prevention (prevention of recurrence in patients with previous episodes of arrhythmia) initially some small prospective studies were published, in which the treatment with only the ACEI [9], or the association of ACEIs or ARBs with chronic antiarrhythmic treatment with amiodarone resulted in a statistically significant reduction in recurrence of AF [10, 11].

However, subsequently, three large prospective studies, randomized with ARB vs. placebo, have instead highlighted an absence of effect of these drugs in preventing AF recurrences in various clinical settings. The GISSI-AF [12], which enrolled 1,442 patients, mainly with underlying heart disease and affected by arterial hypertension, has not shown any efficacy of valsartan in reducing the number of arrhythmic recurrences in a 12-month follow-up. In the valsartan group, 51.4% of patients had at least one AF recurrence vs. 52.1% of the placebo group.

In addition, in the Active study [13] in a population of 1,730 patients with characteristics similar to those of GISSI-AF, irbesartan did not reduce the AF recurrence rate at a 4.1-year follow-up. Finally, in ANTIPAF [14] 425 patients with paroxysmal AF were studied in the absence of structural heart disease at a 12-month follow-up, and olmesartan did not determine any modification of the AF burden.

Based on the above results, it appears that ACEIs and ARBs can modify the underlying heart disease, and in this way reduce the incidence of new-onset episodes of AF (primary prevention) at least in patients with left ventricular dysfunction and/or heart failure. However today, based on a recent meta-analysis [15], the use of ACEIs and ARBs appears not justified in the secondary prevention of AF recurrences , at least outside of what are the other indications for the use of these drugs. It remains to be investigated the possible clinical efficacy in the prevention of AF with aldosterone antagonists, which have an important antifibrotic effect.

Statins, in addition to reducing cholesterolemia, have some pleiotropic effects that can act favorably on the substrate of AF and on atrial remodeling, such as an anti-inflammatory and antioxidant action [16]. In addition, increasing the synthesis of nitric oxide at the endothelial level can play a protective effect on the extracellular matrix. In fact, in some experimental studies, statins have been shown to reduce inflammatory processes and formation of fibrous tissue in the atria, to prevent shortening of refractory periods and slowing-down of conduction and to reduce the duration of AF accesses compared to controls [17, 18].

In the clinic, there are some retrospective and prospective studies on the clinical efficacy of statins in the primary and secondary prevention of AF [19-21]. The data are conflicting and obtained mainly from retrospective studies while the prospective studies are small. Given the anti-inflammatory action of statins, their effect on the prevention of AF in cardiac surgery has been studied in particular. The ARMYDA-360 study has highlighted a significant reduction in the incidence of postoperative episodes of AF in 200 patients randomized to atorvastatin vs. placebo. Although the data are not always confirmed in subsequent studies, in the meta-analysis by Chen et al [22] there is a statistically significant benefit of statins in the prevention of AF in cardiac surgery. Instead, in other clinical situations of primary and secondary prevention, including studies after atrial ablation [23], statins are not proved effective in preventing AF [24].

The data regarding atrial arrhythmias are limited. The first observational study, involving 4,815 subjects aged > 65 years with a follow-up of 12 years [25], showed a reduction of 28-31% of the incidence of AF among subjects with regular fish intake in the diet. These data, however, were not confirmed in two large subsequent studies [26, 27].

Recently three prospective randomized studies centered on the prevention of recurrence of AF have given conflicting results. In the study of Nodari et al [28] in 199 patients with persistent AF, in chronic treatment with amiodarone and ACEIs or ARBs, the addition of n-3 polyunsaturated fatty acid (PUFA) resulted in a statistically significant reduction in arrhythmia relapses after electrical cardioversion. On the contrary, the study by Kowey et al [29] in 663 patients with paroxysmal or persistent AF, showed no effect of n-3 PUFAs in reducing the risk of recurrence of AF. Negative results were also obtained in the study by Bianconi et al [30] in 200 patients after cardioversion of AF.

In a recent meta-analysis [31], relating to 1,955 patients, n-3 PUFA were ineffective in both primary prevention (including AF after cardiac surgery), and secondary AF prevention. This data were confirmed in the results of the OPERA study, which assessed the effect of the administration of n-3 PUFAs on the incidence of AF in the first 10 days after surgery in 1,516 patients for coronary or valvular cardiac surgery. In fact, the incidence of AF was substantially similar in the placebo group compared to the group pretreated with n-3 PUFA [32]. Therefore, in light of these results, there are currently insufficient data to propose n-3 PUFA therapy in the prevention of primary or secondary AF, outside of what are the conventional indications for the use of these drugs.

In the upstream therapy scenario, sacubitril/valsartan enters with a substantially new role. In fact, unlike beta blockers, ACEIs and sartans, this drug is not a neurohormonal blocker, but rather a drug that amplifies and enhances the action of cardiac hormones, namely the atrial natriuretic peptide (ANP) and the B-type natriuretic peptide (BNP), the latter being synthetized by ventricular myocytes in response to increases of wall stretch [33]. Sacubitril/valsartan does not have an intrinsic antiarrhythmic effect; however the increase in the half-life of ANP and BNP that it induces allows these cardioprotective hormones to more intensely regulate the function of the atria and ventricles. This occurs at the level of the atria through a preservation of the reservoir function, that is, the aspiration of caval and pulmonary venous blood into the right and left atrium, respectively, during the ventricular systole [34]. Moreover, at the ventricular level, the drug acts by increasing the global longitudinal strain [35]. In other words, it improves the depressed stroke volume by retrieving the contractile efficiency especially along the sagittal-longitudinal axis, rather than by strengthening the wall kinesis in the radial direction [35]. Thus, the restoration of the hemodynamic balance obtained with sacubitril/valsartan is able to regularize the heart rhythm, by inducing a “reverse remodeling” of the atria both morphologic and electroanatomic.

There is little data on the literature regarding a possible role of sacubitril/valsartan for the prevention of AF [36-38]. In fact, there are currently no randomized controlled trials (RCTs) concerning the use of sacubitril/valsartan for antiarrhythmic purposes. Instead, the case report presented below would seem to support the efficacy of sacubitril/valsartan used as upstream therapy for AF.

The patient described in this report was a woman, aged 35 years, married with two children, and had a history of relapsing episodes of paroxysmal AF, for which flecainide controlled-release was prescribed (January 2017) at the dose of 100 mg once daily. Subsequently, due to the reappearance of AF runs during the 24-h Holter recording, associated with annoying palpitations, the patient was offered the radiofrequency ablation, which she refused. The controlled-release flecainide was therefore cancelled and replaced by the addition of bisoprolol 2.5 mg once daily plus amiodarone 200 mg daily. The echocardiogram (Fig. 1) was characterized by a severely depressed (23%) left ventricular ejection fraction (LVEF) due to uniform dilatation of the left ventricle and moderate secondary mitral insufficiency. Thus, considering the echocardiographic picture compatible with the diagnosis of idiopathic dilated cardiomyopathy, the therapy was supplemented by ramipril at the dose of 5 mg once a day, plus a mineralocorticoid receptor antagonist, i.e., canrenone 25 mg daily, plus furosemide 25 mg daily. In addition, due to the incumbent risk of cardioembolic events related to recurrent paroxysmal AF episodes, the patient was given rivaroxaban at the dose of 15 mg once daily. In January 2018, despite the patient’s close adherence to therapy, she started complaining about dyspnea related to minimal physical activity (New York Heart Association (NYHA) class III). The deterioration of the hemodynamic and clinical picture was related to the worsening of the functional mitral insufficiency and the occurrence of intermittent left bundle branch block. For the worsening mitral regurgitation the patient was offered a MitraClip procedure that she refused (February 2018). The echocardiogram revealed a severe dilation of the left ventricle with end-diastolic volume of 107 mL and end-systolic volume of 82 mL, and severely reduced LVEF (32%) with left atrial volume index (LAVI) of 38 mL/m². During the follow-up, in July 2018, her ventricular function was still severely reduced (LVEF 32%) and LAVI was about 38 mL/m², despite the cardioprotective therapy. Therefore, ramipril was suspended, and after 48 h sacubitril/valsartan therapy was initiated, at the dosage of 24/26 mg twice daily in add-on to therapy with furosemide 25 mg quaque altera die (qod), carvedilol 12.5 mg twice daily, canrenoate 25 mg once daily, and rivaroxaban 20 mg once daily. In February 2019, sacubitril/valsartan was up titrated to 49/51 mg/bis in die (bid). In May 2019, sacubitril/valsartan was up titrated to 97/103 mg/bid, but patient had symptomatic hypotension, so the dosing was reduced to 49/51 mg/bid. At the subsequent follow-up visit, sinus rhythm was restored and LVEF progressively recovered, with a marked reduction of chamber dimensions and cardiac volumes. In May 2019, LVEF was 35%, and LAVI was reduced to 30 mL/m². At present, the patient is in good conditions and furosemide dosing has been curtailed to the 25 mg qod (Fig. 2).

Click for large image

Figure 1. Transthoracic echocardiography (TTE) at the patient’s first visit.

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Figure 2. Echocardiography after 10 months of therapy with sacubitril/valsartan.

The patient whose clinical description constitutes the subject of the present article, gave informed consent to participate in the study, and provided informed consent for publication.

The case illustrated is an example of the efficacious action of sacubitril/valsartan which in a 20-month follow-up has shown to favorably modify the pump efficiency, reduce congestion, antagonize atrial electroanatomical remodeling, thereby favoring the retrieval of the sinus rhythm. In reality, the judgment cannot be generalized to all the decompensated patients since the present study is a case report and not a RCT study. However, our experience, albeit limited, with sacubitril/valsartan used as an upstream therapy for AF leads us to assert that the drug could play a role in preventing AF recurrences through its multiple pharmacodynamic actions, including the antagonism against the renin-angiotensin-aldosterone system (RAAS), the reduction of the ventricles’ hemodynamic overload, the improvement of aspiration of venous caval and pulmonary venous blood respectively by the right atrium and the left atrium thanks to the favorable modulation of atrial compliance by the ANP, whose half-life is increased by sacubitril/valsartan.

Upstream therapy of AF, despite the mixed results reported so far, could have sacubitril/valsartan as its ideal drug, because this molecule acts in a balanced way on the electroanatomic remodeling of the atria thanks to the amplification of the beneficial role of the ANF obtained by the inhibition of the neprilysin which is responsible for its degradation.

The drug, favoring the improvement of the atrial reservoir phase, is able to harmoniously regulate the atrial filling during the systole. The improvement of the mechanical properties of the atrium is then mirrored by an improvement of its electrophysiological properties. Therefore, there is either a greater regularity of the ventricular response or even a restoration of the sinus rhythm, as in the present case of AF converted after the introduction in the therapy of sacubitril valsartan.

Acknowledgments

None to declare.

Financial Disclosure

The authors certify that no funding has been received for the conduct of this study. Novartis Farma SpA, Italy, provided unconditional support for the publication of the manuscript.

Conflict of Interest

The authors Renato De Vecchis, Andrea Paccone and Marco Di Maio have no conflicts of interest that are directly relevant to the content of this study.

Author Contributions

RDV and AP contributed to conceptualization; RDV contributed to data curation; RDV, AP and MDM contributed to writing and original draft preparation; RDV, AP and MDM contributed to writing, review and editing.

Data Availability

The data supporting the findings of this study are available from the corresponding author upon reasonable request.

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