Renal Denervation To Treat Heart Failure
Mar 07, 2022
Abstract
Heart failure (HF) is a global pandemic with a poor prognosis after hospitalization. Despite HF syndrome complexities, evidence of significant sympathetic overactivity in the manifestation and progression of HF is universally accepted. Confirmation of this dogma is observed in guideline-directed use of neurohormonal pharmacotherapies as a standard of care in HF. Despite reductions in morbidity and mortality, a growing patient population is resistant to these medications, while off-target side effects lead to dismal patient adherence to lifelong drug regimens. Novel therapeutic strategies, devoid of these limitations, are necessary to attenuate the progression of HF pathophysiology while continuing to reduce morbidity and mortality. Renal denervation is an endovascular procedure, whereby the ablation of renal nerves results in reduced renal afferent and efferent sympathetic nerve activity in the kidneyand globally. In this review, we discuss the current state of preclinical and clinical research related to renal sympathetic denervation to treat HF.
CISTANCHE WILL IMPROVE KIDNEY/RENAL DISEASE
INTRODUCTION
Heart failure (HF) is a global pandemic, affecting greater than 26 million people worldwide (1) and 6.2 million people in the United States (2). The prevalence of HF is projected to increase 46% by the year 2030 and cost $70 billion in the United States alone (3), while deaths attributable to HF from 2007 to 2017 increased by 42% (2). HF is a complex syndrome, resulting from a variety of pathophysiological conditions that lead to adverse cardiac remodeling and dysfunction. The manifestation of HF is observed as dyspnea upon exertion, fatigue, exercise intolerance, and congestion. It is well established that sympathetic nervous system (SNS) activation is a critical compensatory response to cardiovascular insults, such as acute myocardial infarction, resulting in reduced cardiac function and the inability to maintain cardiac output (4). Initially, activation of the SNS is a beneficial adaptation that serves to maintain blood pressure and perfusion of organs. However, chronic activation of the SNS results in profound pathological consequences that impact the heart and circulation (4). Attenuation of the downstream consequences of pathological overactivation of the SNS has been a therapeutic target for cardiovascular diseases, including hypertension and HF. A number of drugs have been developed to counteract the SNS, including beta-blockers, angiotensin-converting enzyme inhibitors (ACEi), angiotensin II receptor blockers (ARBs), and mineralocorticoid receptor antagonists. Although these agents are effective, their benefits are limited by side effects and poor patient compliance. Furthermore, these agents fail to inhibit the SNS in a significant manner and do not attenuate proximal SNS signals but rather downstream consequences.
Chronic neurohormonal activation may aid the heart in maintaining cardiac output in cardiovascular disease, but it eventually leads to deleterious remodeling and pathological consequences and cellular signaling in the heart, vasculature, and kidneys. The kidneys are a critical regulator of central SNS outflow (5) and contribute to neurohormonal mediator production via the renin-angiotensin-aldosterone system (RAAS) (6). Deranged renal function is well characterized in the progression of cardiovascular disease, including essential hypertension and HF (7, 8). Hypertension is the most common comorbidity associated with cardiovascular mortality worldwide (9). This relationship necessitates the development of novel therapeutics to provide alternative strategies to treat these patients for which pharmacological therapies fail to achieve acceptable reductions in blood pressure.
One attempt to address this treatment gap in hypertension involves the use of catheter-based approaches for renal sympathetic denervation (RDN) as a therapeutic strategy to downregulate both afferent and efferent sympathetic nerve activity (10). This technique is a one-time, minimally invasive, catheter-based procedure that ablates renal sympathetic nerves in a bilateral manner using radiofrequency energy, ultrasound energy, or chemical ablation. RDN has been shown to exert clinically relevant blood pressure–lowering effects in patients with hypertension (11–13). While initial clinical trials were positive, these trials were not blinded appropriately and lacked sham controls (14, 15). A subsequent trial (16) involving a sham treatment arm and appropriate blinding of study subjects failed to demonstrate a significant reduction in blood pressure in hypertensive patients. More recently, newer RDN catheters have been developed for clinical use, users have gained more experience with experimental RDN devices, and clinical trial designs have been modified and optimized to involve the most responsive patient populations. It has now become clear that RDN does significantly reduce blood pressure in the setting of hypertension. Despite the focus of catheter-based RDN therapy for resistant hypertension, basic research investigating this modality in the context of HF has come to the forefront (17, 18). This review summarizes the current state of preclinical and clinical research related to the use of RDN and alternative autonomic modulatory approaches to treat HF.
Keywords: sympathetic nerve system; heart failure; cardiorenal syndrome; renal denervation; hear failure with preserved ejection fraction; Renal, Kidney
REGULATION OF SYMPATHETIC NERVOUS SYSTEM IN HEART FAILURE
HF is characterized by the inability of the heart to maintain cardiac output and appropriate organ perfusion (19). Changes in cardiac output and blood pressure are detected by both mechano and chemoreceptors within the circulation that relay this information to cardiovascular centers in the central nervous system (20). Information provided by the chemo- and pressure receptors is integrated to regulate cardiac, renal, and vascular function maintaining blood pressure within the normal, physiological range via the level of activation of the parasympathetic and sympathetic nervous systems. In the setting of HF (Figure 1), the SNS is activated maximally and inappropriately as a result of a significant reduction in cardiac output and blood pressures resulting in under perfusion of organs throughout the body. In this case, sustained activation of cardiac sympathetic efferent nerves results in pathological cardiac hypertrophy, fibrosis, and arrhythmias. The vasculature (macro- and microcirculation) is subject to endothelial cell dysfunction, smooth muscle cell hypertrophy, and vasoconstriction following activation of the sympathetic nerves innervating the vasculature. Finally, increased renal sympathetic activity augments sodium reabsorption, renal release of renin and activation of the RAAS, and renal injury. Pathological effects in the kidneys following renal SNS activation ultimately increase circulating blood volume, tissue edema, and systemic vasoconstriction via angiotensin II to significantly exacerbate HF.
CISTANCHE WILL IMPROVE KIDNEY/RENAL FUNCTION
A HISTORICAL PERSPECTIVE ON RENAL DENERVATION
In 1924, the first surgical renal denervation procedure was performed by Papin & Ambard (21) as an intervention for nephralgia and limited hydronephrosis. In four of six cases of surgical renal denervation, pain was relieved; however, in all cases here, hydronephrosis was not controlled(21). A decade later, in 1934, prior to the era of antihypertensive drugs, the first case of surgical renal denervation was performed in a patient with uncontrolled hypertension and nephritis (22). Surgical denervation in this patient did not lead to a drop in blood pressure and had no effect on renal function (22). A subsequent follow-up study, in 1935, demonstrated a drop in blood pressure over weeks and months; however, blood-pressure-lowering effects were not permanent (23). The authors concluded in four of the five cases, renal denervation (a) attenuated proteinuria, (b) preserved renal efficiency in clearance on urea, and (c) despite initial blood pressure–lowering effects, had no major effect on blood pressure over time (23). In 1953, a clinical research study of 1,266 patients suffering from essential hypertension that underwent splanchnicectomy were assessed for blood pressure–lowering effects and subsequent mortality (24). The results demonstrated a 45% reduction in arterial blood pressure at the 5-year postoperative follow-up; however, the authors emphasized a hesitation in choosing surgical methods over drug therapy due to a lack of superiority(24). Furthermore, surgical patients suffered from complications, including orthostatic hypotension, impotence, and incontinence. Consequentially, sympatholytic surgery became obsolete with the development of more tolerable and efficacious antihypertensive pharmacotherapies (24).
CATHETER-BASED RENAL DENERVATION IN THE ERA OF INTERVENTIONAL CARDIOLOGY
The first attempts to modulate autonomic nervous system activity using a percutaneous endovascular catheter approach were performed in a preclinical model of atrial fibrillation (25). The study authors sought to control heart rate through interruption of the parasympathetic nervous system. Schauerte et al. (25) demonstrated that atrial radiofrequency ablation abolished vagal-driven atrial fibrillation. This work provided proof-of-concept results for the concept of implementing radiofrequency energy-based catheter devices through an interventional approach. The first adoption of a radiofrequency energy ablation catheter to denervate the kidneys was by Ardian, Inc., a US-based company acquired by Medtronic, Inc. Vascular safety was first demonstrated by preclinical studies in a porcine model (26). The Symplicity® catheter was utilized in a safety and proof-of-concept clinical trial published in 2009 (27). This catheter system and clinical trial were the cornerstones for the development of several other systems over the next decade, including five radiofrequency-based catheters: Symplicity Flex® and Spyral® (Ardian-Medtronic); EnligHTN® (previously St. Jude Medical, now Abbott); V2 (Vessix Vascular®; Boston Scientific); and RENLANE® (Cordis Corporation); one ultrasound-based catheter, Paradise® (ReCor Medical); and one chemical ablations catheter, Peregrine System® (Ablative Solutions). As the catheters were developed, the focus became on designing catheters with multielectrode for more complete circumferential denervation and catheter maneuverability for potential tortuous vasculature. New catheter designs and modifications resulted in more reliable and efficacious RDN in hypertensive patients. Despite initial success in treating hypertension, the development of RDN was not without its misfortunes and failures. Over the last decade, obstacles regarding the technology, clinical trial design, patient selection, and appropriate study endpoints have severely hampered the clinical translation of this promising technology.
Following the failure of the Symplicity HTN-3 study, several rigorous follow-up clinical trials demonstrated efficacy. These have sparked renewed interest in the therapeutic potential of RDN for hypertension. Some of these trials include the SPYRAL HTN-OFF (13) (NCT02439749) and ON MED (NCT02439775) trials (12), and the RADIANCE-HTN SOLO/TRIO trial (NCT02649426) (11). These trials all have similar designs, with rigorous inclusion/exclusion criteria (28) and established procedures that would permit the maximum effect of RDN to be observed on lowering blood pressure. These more recent clinical trials have demonstrated significant and clinically relevant reductions in blood pressure compared to sham controls (11–13). Careful design and well-executed trials have reestablished RDN’s ability to provide clinically meaningful blood pressure–lowering effects. This opened the door for alternative denervation systems, like the Peregrine catheter, whereby alcohol ablation of the renal interstitium is performed. Ongoing clinical trials in the United States and Europe are currently evaluating the safety and efficacy of this device (NCT02910414 and NCT03503773). Moreover, pivotal trials are now underway, such as SPYRAL PIVOTAL– SPYRAL HTN-OFF MED (NCT02439749) trial and the RADIANCE II Pivotal Study (NCT03614260), with completion dates expected in 2022 and 2024, respectively.
RENAL SYMPATHETIC DENERVATION IN HEART FAILURE WITH REDUCED EJECTION FRACTION
HF with a reduced ejection fraction (HFrEF) [left ventricular ejection fraction (LVEF) <40%] (29) is primarily characterized by a significant deficit in the systolic function of the heart, with or without congestion depending on the progression of the HF syndrome. Previous research (30) has demonstrated a substantial increase in renal norepinephrine spillover in HF patients. When compared to individuals with essential hypertension (31), the levels of norepinephrine spillover from the kidneys in HF patients are significantly higher (30), suggesting increased SNS activity. Increases in muscle sympathetic nerve activity were positively correlated to increased HF severity and demonstrated a tenfold increase in peripheral muscle sympathetic nerve activity (32). The effectiveness of neurohormonal modulators, such as beta-blockers, ACEi, ARBs, aldosterone antagonists, diuretics, and neprilysin inhibition, as standards of care to manage HFrEF, is a testament to the significant role the SNS plays in exacerbating HF severity (9, 33–35). Despite the success of these pharmacotherapies in reducing morbidity and early mortality, resistance to pharmacotherapies, off-target side effects, and the lack of patient adherence to drug regimens (36, 37) still lead to worsened HF symptoms over time. It should also be noted that the currently available drugs to treat HFrEF do delay the progression of the disease, but they do not halt or reverse this condition. Therefore, a clinically unmet need for adjunctive or alternative therapeutic strategies to combat HFrEF still exists.
Preclinical studies have investigated the potential beneficial effects of RDN in the setting of myocardial ischemia-reperfusion and asymptomatic HFrEF (17, 18, 38). In a spontaneously hypertensive rat model, Polhemus et al. (38) investigated the role of RDN on SNS modulation in ischemia-reperfusion injury to evaluate the potential acute cardioprotective effects of renal sympathetic denervation. This study elucidated the novel remote preconditioning cardioprotective mechanisms of RDN in the setting of ischemia-reperfusion in conjunction with chronic hypertension. The results demonstrate a significant reduction in myocardial infarct size and preservation of cardiac function 7 days postreperfusion following RDN pretreatment as compared to sham control (38). RDN treatment in spontaneously hypertensive rats resulted in marked attenuation of oxidative stress, reduced G protein-coupled receptor kinase 2 (GRK2) pathological signaling in the heart, and increased myocardial nitric oxide bioavailability (38).
Subsequent studies involved investigations into the effects of RDN in HFrEF following acute myocardial infarction. Polhemus et al. (17) report on the beneficial effects of delayed radiofrequency RDN to improve outcomes in the setting of HFrEF in rats subjected to myocardial ischemia and reperfusion. This study was performed in both spontaneously hypertensive and normotensive Wistar Kyoto rats who underwent 45 min of myocardial ischemia followed by 12 weeks of reperfusion. At 4 weeks, following myocardial infarction, the rats were randomized to sham RDN or radiofrequency RDN. The radiofrequency RDNtreated animals displayed significant improvement in left ventricular function, vascular reactivity, and reduced cardiac fibrosis. Furthermore, these investigators observed greater than twofold increases in plasma levels of natriuretic peptides [NPs; B-type (BNP), atrial (ANP), and C-type (CNP)] that were mediated via inhibition of renal neprilysin activity (17).
CISTANCHE WILL IMPROVE KIDNEY/RENAL INFECTION
To evaluate the clinical potential of radiofrequency RDN in the setting of chronic HFrEF, we recently embarked on experiments utilizing a swine model of HF secondary to acute myocardial infarction (18). These studies utilized the St. Jude EnligHTN radiofrequency RDN system to perform circumferential RDN in both the proximal and distal regions of the renal arteries following the onset of HFrEF at a time when LVEF was significantly reduced. Normotensive Yucatan mini-swine underwent 75 min of myocardial ischemia and subsequent reperfusion for 18 weeks. After the manifestation of reduced LVEF (<40%), animals were randomized in a blinded manner to receive sham RDN or radiofrequency RDN treatment and 12 weeks of follow-up. There was a significant reduction in renal norepinephrine, a biomarker of renal sympathetic nerve activity, and highly significant reductions in both circulating angiotensins I and II following radiofrequency RDN treatment (18). These data confirm robust inhibition of renal sympathetic nerve activity coupled with attenuation of renal renin-angiotensin system activation as a key beneficial effect of RDN in HF. This swine study confirmed earlier results obtained in the rat study (17) as evidenced by increased NP levels and improved left ventricular structure and function after radiofrequency RDN when compared to sham RDN. We also observed improved coronary artery vasorelaxation to endothelial-dependent and -independent vasodilators. Similar findings have been reported by others in both small (39–41) and large (42, 43) animal HFrEF models. Figure 2 summarizes our findings on the protective actions of radiofrequency RDN in rodent and swine studies of HFrEF secondary to acute myocardial infarction.
One of the unexpected findings from studies of RDN in HFrEF is the effect of RDN to inhibit neprilysin in the kidney during HF to augment the bioavailability of NPs and improve myocardial and vascular function. NPs are a well-established biomarker of HF severity (44–46). It was discovered four decades ago that the heart was an endocrine organ (47), producing and secreting a family of hormones known as NPs (48–50). NPs' primary mechanism of action is the reduction of cardiac preload and afterload to ultimately reduce myocardial wall stress that occurs as HF progresses in severity (51). Dilatation of the left ventricular chamber and wall thinning promote increased stretch that is sensed by ventricular myocytes, stimulating NP secretion. NPs signal to the vasculature, which induces smooth muscle relaxation-mediated vasodilation to reduce peripheral vasculature resistance. In the kidney, it promotes natriuresis and diuresis to reduce blood volume, subsequently reducing arterial pressure in an attempt to correct pathological myocardial wall tension (52). In addition, the autocrine effects of NPs elicit cardioprotective signaling within the heart. NPs signal through NP receptors A, B, and C (53, 54). Two of the receptors (A and B) are G protein-coupled, activating guanylyl cyclase generation of cyclic guanosine monophosphate (53, 55). This signaling cascade leads to activation of protein kinase G (56), which has been shown to inhibit hypertrophic remodeling and improve cardiac contractility (57, 58). NPs can also attenuate transforming growth factor-beta activation of fibroblasts within the myocardium, leading to attenuation of fibrosis (59). Figure 3 summarizes the powerful cardioprotective effects that can occur with increased circulating NPs (52).
Following RDN in the setting of HFrEF we found that the primary enzyme responsible for NP degradation, neprilysin, was significantly inhibited (17, 18). Neprilysin is a membrane metalloendopeptidase found primarily in the kidney and lungs that cleaves hormone peptides (60). In Figure 4, our hypothesis suggests that the SNS plays a critical role in renal neprilysin activity, which subsequently affects NPs as described. Under conditions of chronic SNS overactivation, it is our belief that renal β1-adrenergic signaling increases neprilysin activity, through posttranslational modifications that have yet to be defined. This leads to increased degradation of NPs and a loss of cardioprotective effects permitting further adverse cardiovascular remodeling and worsening HF. Neprilysin inhibition is at the forefront of current HF treatment strategies(61). Sacubitril, a neprilysin inhibitor combined with the ARB valsartan, has been shown to be highly effective in HFrEF to reduce cardiovascular mortality. In the PARADIGM-HF study (62), sacubitril/valsartan reduced combined primary endpoints of cardiovascular death and hospital admission by 20% when compared to enalapril in 8,442 patients with HFrEF. Interestingly, radiofrequency RDN not only inhibits neprilysin activity but very significantly halts activation of the renin-angiotensin system, resulting in low circulating levels of angiotensin I and II (17, 18). These data suggest that RDN acts in a very similar manner to the combination therapy of neprilysin inhibition and angiotensin receptor blockade (i.e., LCZ696, sacubitril/valsartan). One potential advantage of RDN over LCZ696 is that RDN would only need to be performed once as opposed to daily drug dosing over many years.
Cardiac arrhythmias are a result of complex autonomic dysregulation of the electrophysiological circuitry within the heart under pathophysiological conditions. Many cardiac arrhythmias are associated with an imbalanced increase in SNS activity and withdrawal of parasympathetic regulation (63). The desynchrony within the heart can lead to adverse cardiac remodeling, perpetuating a sustained and chronic arrhythmogenic state, such as recurrent ventricular tachycardia or atrial fibrillation. The incidence of ventricular tachycardia is associated with ischemic and nonischemic insults, whereby disruption in the cardiac conduction pathways occurs due to myocardial tissue loss and increased fibrosis seen with ischemia or hypertrophic remodeling as occurs in heart failure (64–66). Since RDN can potentially modulate global sympathetic tone without side effects of hemodynamic disarrangement, this procedure may be beneficial in this context. In a proof-of-principle murine model of myocardial ischemia-induced HF, chemical RDN with phenol resulted in reduced susceptibility of ventricular arrhythmias (39). The translational application of this work to a porcine model of myocardial ischemia validated the use of RDN to significantly suppress ventricular tachycardia when compared to sham-operated animals (67). In cases where cardiac sympathetic denervation failed and persistent refractory ventricular tachycardia is present, interventionists are performing adjunctive RDN to cardiac sympathetic denervation procedures. In 10 patients with cardiomyopathies (20% ischemic) and HFrEF, Bradfield et al. (68) demonstrated the potential benefit of cardiac sympathetic denervation with adjunctive RDN when compared to cardiac denervation alone, whereby a significant reduction in cardioverter-defibrillator shocks was seen in patients 6 months postRDN. The authors also concluded that RDN following cardiac denervation is indicative of poor prognosis (68). Additional case reports and clinical studies have been performed aiming to understand the efficacy of RDN as primary or adjunctive therapy in patients suffering from dilated and hypertrophic cardiomyopathy as well as refractory ventricular tachycardia after myocardial ischemia (69, 70). Large-scale prospective studies are necessary to validate RDN in this context.
A unique and potentially important aspect of RDN compared to current pharmacological therapies is that RDN’s site of action to inhibit renal norepinephrine is upstream of pharmacotherapy used today in HF (e.g., ACEi, ARBs, beta-blockers). Current drug therapies work to disrupt intermediate-level signaling and end-organ receptors, and this approach fails to address critical and proximal pathological signals that drive the pathology of HF and disease progression. In contrast, RDN modulates renal afferent signaling to the central nervous system and inhibition of efferent signaling to the kidney and potentially other organs. Reduction of norepinephrine levels in target tissues and spillover into the circulation inhibit maladaptive sympathetic signaling and its downstream signaling pathways (β1-adrenergic signaling, RAAS activation, increased neprilysin activity, reduced circulating NPs), providing beneficial effects on HF progression.
Despite the overwhelming positive preclinical data in HFrEF and clinical data in hypertension, little has been done clinically to evaluate the safety and efficacy of RDN in HFrEF patients. Davies et al. (71) published the first-in-man clinical trial evaluating RDN in chronic systolic HF (REACH Pilot study; NCT01584700). In 7 patients, there was improved HF symptoms and exercise capacity, as measured by a 6-min walk test at 6 months postRDN with no adverse events (71). This trial preceded the results of the Symplicity HTN-3 study. In 2013, the PRESERVE clinical trial (NCT01954160) was initiated to study the safety, efficacy, and effect of RDN on renal sodium excretion in HFrEF patients but was abruptly terminated by the Data and Safety Monitoring Board when the Symplicity HTN-3 results were published. Since then, there has been a paucity of data in alternative indications like HFrEF.
RENAL SYMPATHETIC DENERVATION IN HEART FAILURE WITH PRESERVED EJECTION FRACTION
A recent reevaluation of the dichotomy within the HF population has shed light on the ever-growing number of patients that present with classical HF symptoms (dyspnea, fatigue, lack of functional reserve) yet maintain a preserved ejection fraction (HFpEF) (LVEF >50%) (29). HFpEF is a systemic syndrome consisting of multiorgan pathophysiological abnormalities and driving end-organ damage, including cardiovascular remodeling and exertional intolerance (72). Of importance, exclusion of other causes of HFpEF or dyspnea must be ruled out, including but not limited to valvular disease, pericardial disease, and infiltrative myocarditis (73). HFpEF accounts for more than half of all HF diagnoses, and treatments for this rapidly developing disease are extremely limited, as no US Food and Drug Administration (FDA)-the approved drug has been shown to be effective in the setting of HFpEF (74). Neurohormonal therapies such as ACEi (75), ARBs (76, 77), and aldosterone antagonist (78), as well as combination therapy, are efficacious in HFrEF (79) but have uniformly failed to provide meaningful benefit in HFpEF patients (80). Furthermore, nitric oxide donors (81) and soluble guanylate cyclase activators (82) have been tested in clinical trials and were found to be neutral compared to optimal medical therapy. It is becoming increasingly clear that HFpEF is driven, to some degree, by a distinct subset of pathophysiology mechanisms (74). SNS activity has been shown to be elevated in HFpEF patients(83), but what cannot be discerned is which process is the cause and/or result of the other.
CISTANCHE WILL IMPROVE KIDNEY/RENAL DIALYSIS
HFpEF is recognized as a systemic syndrome that involves an inflammatory response propagated by comorbidities, including hypertension, diabetes mellitus, obesity, and kidney disease, which ultimately lead to HF characterized by diastolic dysfunction. Dependent upon the predominating organ system affected, the clinical presentation of HFpEF can vary widely. Phenomapping, through computer-based algorithms (84), has revealed the dominant phenotypes that are presented clinically; however, no two patients are the same, and with a lack of therapeutic interventions comes a need to develop new strategies and preclinical models for testing safety and efficacy. Herein, we discuss the potential mechanisms by which RDN might be able to impact the most predominant etiologies of HFpEF pathobiology.
With the ever-evolving clinical knowledge base about HFpEF, it has been a struggle for basic researchers to come to a consensus on proper models to elucidate the pathology of this complex disease and for the testing of novel therapeutic strategies. Small (85) and large (86) animal models have been proposed to date, yet each has noteworthy limitations, with little agreement on the interpretation of results (87, 88). An understanding of the target phenotype within HFpEF should be taken into consideration in model development; for instance, a model of cardiometabolic HFpEF. Furthermore, clinical translation must be at the forefront of model development and study design. Although proof-of-concept work in rodent models may elucidate mechanisms, it rarely translates to humans with respect to pathophysiological and therapeutic responses (89). We believe that furthering our understanding of the underlying causes, along with developing and refining rigorous animal models, will begin to allow for some agreement among basic and clinical researchers alike. Figure 5 illustrates the potential beneficial effects that RDN might exert in HFpEF, leading to improved HF symptoms. The sympathetic tone is strongly associated with HFpEF along with all the chronic comorbidities, including metabolic syndrome, hypertension, chronic kidney disease, pulmonary hypertension, and atrial fibrillation (90–94). End-organ dysfunction at the level of the heart, lungs, vasculature, kidneys, and skeletal muscle could be attenuated with RDN modulation of SNS activity. Future preclinical and potentially clinical studies are required to test the efficacy of RDN in the setting of HFpEF, and given the diverse and highly complex nature of the HFpEF patient population, it is critical to determine which HFpEF patients suffer from SNS overactivation and might be responsive to RDN therapy.
In the setting of HFpEF, increasing NPs through RDN-induced neprilysin inhibition may be an effective way to increase protein kinase G signaling and improve outcomes via the impact on a number of organs, including the heart. Clinical trials have targeted neprilysin inhibition using a combination of sacubitril/valsartan (LCZ696) as compared to valsartan in HFpEF patients. The PARAGON-HF trial (NCT01920711) (79) enrolled 4,822 patients randomized to a combination of valsartan-only therapy. The study demonstrated no significant difference in the rate of hospitalization or cardiovascular-related mortality between treatment groups (79). Despite neutral results, this mechanism of action may still be a viable target if RDN is applied. We stress the concept that RDN works more proximally on the underlying issue of SNS overactivation by inhibiting renal afferent and efferent signaling, which can provide remote cardioprotective effects in conjunction with neprilysin inhibition.
Small retrospective analyses and observational clinical research have been performed to examine RDN in patients with HFpEF. In a randomized clinical trial of resistant hypertension, a quarter of the patients were clinically diagnosed with HFpEF and received RDN (95). Brandt et al. (95) reported that at 6 months after RDN, the RDN-treated patients had a reduced left ventricular mass, improved systolic function, and indexes of diastolic function (mitral E deceleration time, E/e′ ratio) as compared to optimal medical therapy. In a recent multicenter cardiac magnetic resonance (CMR) imaging study (96), 16 patients with resistant hypertension and diagnosed HFpEF underwent RDN. There was a significant improvement in global longitudinal strain, suggesting an improved diastolic function in these patients. While CMR imaging is a more reliable imaging modality, with less interobserver error, large clinical trials with long-term follow-up are truly necessary for more concrete conclusions to be made. The RDT-PEF randomized clinical trial (NCT01840059) (97) was going to take on this task; however, due to difficulties in recruitment the study was unpowered to demonstrate improvement in quality of life, exercise, and biomarker and cardiac remodeling. However, in those patients enrolled, the procedure was safe (97). As the field of catheter-based denervation garners regulatory approval for its primary indications, the flood gates might soon open on alternative indications, such as HFpEF. Only then will we begin to get answers on clinical efficacy in an ever-growing HF population.
ALTERNATIVE STRATEGIES FOR AUTONOMIC MODULATION IN HEART FAILURE
Renal integration into the SNS has a major impact on the autonomic nervous system in health and disease, and RDN is poised to become an effective procedure to combat sympathetic overactivity observed in a myriad of disease conditions. Notwithstanding, RDN is not the only technology under development to attenuate sympathetic overactivity to treat hypertension or cardiovascular diseases. Other technologies are being developed to target more centrally located autonomic integration centers, including the baroreceptor reflex (98– 100), as well as vagal parasympathetic innervation (101, 102). The MobiusHD®, by Vascular Dynamics, Inc. is a proprietary-designed device that is placed through an endovascular procedure in the internal carotid artery to create a geometric alteration on the carotid bulb, leading to changes in the carotid sinus nerve input to the central nervous system. The device is termed an endovascular baroreflex amplification technology. The baroreceptor reflex, over time, is lost or “reset” in patients with essential hypertension (103). This device, when implanted, changes the pulsatile strain of the carotid bulb, thereby inducing a reduction in blood pressure. The first patient procedure was performed in 2015 and reported a blood pressure-lowering effect in a single patient with resistant hypertension (100). A first-in-man, multicenter, prospective, open-labeled trial (CALM-FIM_EUR; NCT01900897) reported a significant blood pressure-lowering effect in 30 patients with resistant hypertension (104). The study demonstrated that the MobiusHD device also had an acceptable safety profile; however, it did have adverse events in four patients (104) (i.e., hypotension, worsening hypertension, intermediate claudication, and one wound infection). There are four active/nonrecruiting studies, one of which is the CALM-2 pivotal study (NCT03179800), which is estimated to enroll 300 patients and measure changes in 24-h systolic arterial blood pressure from baseline to 180 days. The MobiusHD is not the only device that targets the baroreflex.
CVRx, Inc. developed a technology that activates the baroreflex through an implantable pulse generator and a lead system called Rheos® (98). The technology was initially conceived as an alternative therapeutic intervention for resistant hypertension (105). The device is implanted subcutaneously and sends pulse waves to the lead implanted near the carotid bodies to rectify the autonomic imbalance in patients. To understand the implications of baroreflex activation in the pathogenesis of HF, the device is being tested in current clinical trials (NCT00957073, NCT01471860, and NCT01720160). Initial reports (99, 106) demonstrate improved quality of life, 6-min walk test, and LVEF, and a reduction in HF hospitalization in NYHA Class III HF patients. Others have taken a different approach to understanding the autonomic imbalance by directing effort to stimulate the vagal nerve and induce parasympathetic activation. While several clinical trials have been performed (101, 102), data would suggest that safe, favorable, or neutral outcomes were observed in patients over long-term follow-up. Results demonstrate an improvement in HF symptoms but no difference in mortality (101, 102).
Other devices are taking an indirect approach at providing autonomic modulation. A hallmark of HF, observed clinically, is congestion, both pulmonary and/or peripheral (19, 29). Cardiac shunt devices are being implemented in hope of providing congestion relief in HF patients. Although they do not directly affect the SNS, strategically placed shunts may elicit changes in arteriovenous hemodynamics and shift blood volume. By centrally unloading the left atria, it may permit the left ventricle to work more efficiently. These alterations are sensed by the autonomic sensory afferent nerve, which becomes integrated in the central nervous system, thereby affecting SNS efferent signaling to the cardiopulmonary and cardiovascular systems.
Regardless of whether a patient suffers from HFrEF or HFpEF, increased left atrial pressure and pulmonary congestion are precipitating symptoms of symptomatic and acute decompensated HF; therefore, these shunting devices should be beneficial for both forms of HF. Several studies (107–109) have demonstrated the utility of performing a permanent interatrial shunt. Providing left atrial decompression relieves the pulmonary vasculature from edema and results in better gas exchange and, ultimately, a relief of dyspnea at rest and upon exertion. While most reports have focused on the implementation of this device in HFpEF (107, 108), owing to the lack of efficacious therapeutics, there is a limited data set in the HFrEF population (109). The V-wave clinical study followed HF patients (n = 38) with interatrial shunts for 1 year (109). This first-in-man clinical study deployed a proprietary designed interatrial V-shaped shunt in HF patients with an NYHA class of III or IV; 30 of the patients were diagnosed with HFrEF, while 8 suffered from HFpEF (109). The results demonstrated an improvement in NYHA class, quality of life, and 6-min walk test with no changes in left- or right-sided cardiac function (109). The improvement in the 6-min walk test, which is a metric of the cardiovascular reserve, provides evidence that the shunt not only results in cardiac unloading but also reduces dyspnea. This sustained unloading over time elicits changes systemically (potentially to sympathetic tone), which provides a remote mechanism(s) of cardiovascular protection. In this study (109), the major limitation was shunt closure over time; at 3 months, all devices were patent; however, at 12-months, ~50% were occluded or became stenotic. Patients with patent shunts exhibited sustained cardiovascular benefits through the 12-month study duration (109). Second-generation shunts are currently under development, which will hopefully help to overcome this obstacle; furthermore, large-scale, randomized clinical trials with long-term follow-up are necessary. It is important to investigate all viable options with respect to adjunctive therapeutic strategies to optimal medical therapy to combat the development, manifestation, and severity of HF.
CONCLUSION
HF, a clinical syndrome with several manifestations, has a complex and incompletely understood pathophysiology at play that results in significant morbidity and mortality. The prevalence of HF and the resultant economic burden this disease imposes will continue to rise worldwide, and no guideline-based optimal medical therapy has proven to halt or reverse disease progression for those who suffer from HFrEF. Approved HFrEF therapies only treat HF symptoms but fail to reverse this devastating disease. The current state of affairs is even bleaker for HFpEF, with a complete lack of effective agents to treat this form of HF. There is an abundance of basic and clinical research demonstrating the powerful compensatory and subsequent maladaptive response of the autonomic nervous system to cardiovascular injury and HF. To that end, currently, drug-based neurohormonal modulation is our best therapeutic intervention. Still, there are several limitations to these agents, including the lack of effect in some patients, pharmacotherapy resistance, untoward side effects, and a lack of patient adherence to the drug regimen. With this landscape, it is imperative to develop and test novel therapeutic strategies in the setting of HF.
The kidneys play a critical role in SNS activity and modulation. Therapeutically targeting renal afferent and efferent sympathetic nerves, through RDN, has provided an alternative strategy that is performed remotely but delivers central modulation of the autonomic nervous system and cardioprotective and vasculoprotective effects in HF. Through simultaneous inhibition of the renal afferent and efferent activity, RDN may reset central nervous system integration and therefore global efferent output. Furthermore, by dampening sympathetic efferent signaling to remote targets and the kidney, RDN modulates global catecholamine signaling pathways improves global physiology and halts the maladaptive activation of the renal neurohormonal axes at its origin. Therapeutic mechanisms by which RDN improves outcomes in preclinical models of HFrEF have yet to be fully elucidated and are the subject of ongoing research efforts.
