Renal denervation in patients with heart failure secondary to Chagas' disease: A pilot randomized controlled trial.


Journal

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions
ISSN: 1522-726X
Titre abrégé: Catheter Cardiovasc Interv
Pays: United States
ID NLM: 100884139

Informations de publication

Date de publication:
01 Oct 2019
Historique:
received: 27 04 2019
accepted: 27 06 2019
pubmed: 25 7 2019
medline: 19 8 2020
entrez: 24 7 2019
Statut: ppublish

Résumé

Chagas disease is one of the most relevant endemic parasitic diseases in Latin America, affecting approximately 6 million people. Overt Chagas heart disease is an ominous condition, occurring in 20-30% of infected individuals, which has besides the persistent myocarditis a peculiar intracardiac ganglionic neuronal depletion and dysautonomy. This study aims to evaluate the safety and feasibility of renal denervation for patients with advanced symptomatic Chagas cardiomyopathy. Open-label prospective pilot study that randomized patients with Chagas heart disease to either renal denervation or conservative treatment (2:1 ratio). The primary endpoint was the incidence of major adverse events at 9 months, defined as a composite of all-cause death, myocardial infarction, stroke, need for renal artery invasive treatment, or worsening renal function. A total of 17 patients were allocated for renal denervation (n = 11) or conservative treatment (n = 6). Included patients had severe symptomatic heart disease, with markedly depressed left ventricular function (average ejection fraction 26.7 ± 4.9%). For patients randomized to renal denervation, the procedure was performed successfully and uneventfully. After 9 months, the primary endpoint occurred in 36.4% of patients in the renal denervation group and 50.0% in the control arm (p = .6). After 9 months, clinical, laboratory, functional, echocardiographic, and quality of life parameters were similar between groups. This pilot study suggests that renal denervation is safe and feasible in patients with Chagas cardiomyopathy, warranting future studies to better evaluate the clinical efficacy of the interventional strategy in improving the prognosis of this high-risk population.

Identifiants

pubmed: 31334914
doi: 10.1002/ccd.28393
doi:

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

644-650

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Références

Bocchi EA, Bestetti RB, Scanavacca MI, Cunha Neto E, Issa VS. Chronic Chagas heart disease management: from etiology to cardiomyopathy treatment. J Am Coll Cardiol. 2017;70:1510-1524.
Bern C. Chagas' disease. N Engl J Med. 2015;373:456-466.
Bern C, Montgomery SP. An estimate of the burden of Chagas disease in the United States. Clin Infect Dis. 2009;49:e52.#x2010;e54.
Rassi A Jr, Rassi A, Marcondes de Rezende J. American trypanosomiasis (Chagas disease). Infect Dis Clin North Am. 2012;26:275-291.
Bocchi EA, Arias A, Verdejo H, et al. The reality of heart failure in Latin America. J Am Coll Cardiol. 2013;62:949-958.
Bestetti RB, Muccillo G. Clinical course of Chagas' heart disease: a comparison with dilated cardiomyopathy. Int J Cardiol. 1997;60:187-193.
Espinosa R, Carrasco HA, Belandria F, et al. Life expectancy analysis in patients with Chagas' disease: prognosis after one decade (1973-1983). Int J Cardiol. 1985;8:45-56.
Mady C, Cardoso RH, Barretto AC, da Luz PL, Bellotti G, Pileggi F. Survival and predictors of survival in patients with congestive heart failure due to Chagas' cardiomyopathy. Circulation. 1994;90:3098-3102.
Freitas HF, Chizzola PR, Paes AT, Lima AC, Mansur AJ. Risk stratification in a Brazilian hospital-based cohort of 1220 outpatients with heart failure: role of Chagas' heart disease. Int J Cardiol. 2005;102:239-247.
Davila DF, Rossell O, de Bellabarba GA. Pathogenesis of chronic Chagas heart disease: parasite persistence and autoimmune responses versus cardiac remodelling and neurohormonal activation. Int J Parasitol. 2002;32:107-109.
Khoury AM, Davila DF, Bellabarba G, et al. Acute effects of digitalis and enalapril on the neurohormonal profile of chagasic patients with severe congestive heart failure. Int J Cardiol. 1996;57:21-29.
Mocelin AO, Issa VS, Bacal F, Guimaraes GV, Cunha E, Bocchi EA. The influence of aetiology on inflammatory and neurohumoral activation in patients with severe heart failure: a prospective study comparing Chagas' heart disease and idiopathic dilated cardiomyopathy. Eur J Heart Fail. 2005;7:869-873.
Iosa D, DeQuattro V, Lee DD, Elkayam U, Palmero H. Plasma norepinephrine in Chagas' cardioneuromyopathy: a marker of progressive dysautonomia. Am Heart J. 1989;117:882-887.
Davila DF, Bellabarba G, Hernandez L, et al. Plasma norepinephrine, myocardial damage and left ventricular systolic function in Chagas' heart disease. Int J Cardiol. 1995;52:145-151.
Vogiatzakis N, Tsioufis C, Georgiopoulos G, et al. Effect of renal sympathetic denervation on short-term blood pressure variability in resistant hypertension: a meta-analysis. J Hypertens. 2017;35:1750-1757.
Townsend RR, Mahfoud F, Kandzari DE, et al. Catheter-based renal denervation in patients with uncontrolled hypertension in the absence of antihypertensive medications (SPYRAL HTN-OFF MED): a randomised, sham-controlled, proof-of-concept trial. Lancet. 2017;390:2160-2170.
Kandzari DE, Bohm M, Mahfoud F, et al. Effect of renal denervation on blood pressure in the presence of antihypertensive drugs: 6-month efficacy and safety results from the SPYRAL HTN-ON MED proof-of-concept randomised trial. Lancet. 2018;391:2346-2355.
Fukuta H, Goto T, Wakami K, Ohte N. Effects of catheter-based renal denervation on heart failure with reduced ejection fraction: a systematic review and meta-analysis. Heart Fail Rev. 2017;22:657-664.
Sharp TE 3rd, Polhemus DJ, Li Z, et al. Renal denervation prevents heart failure progression via inhibition of the renin-angiotensin system. J Am Coll Cardiol. 2018;72:2609-2621.
Polhemus DJ, Trivedi RK, Gao J, et al. Renal sympathetic denervation protects the failing heart via inhibition of neprilysin activity in the kidney. J Am Coll Cardiol. 2017;70:2139-2153.
Linz D, Hohl M, Elliott AD, et al. Modulation of renal sympathetic innervation: recent insights beyond blood pressure control. Clin Auton Res. 2018;28:375-384.
Davis MI, Filion KB, Zhang D, et al. Effectiveness of renal denervation therapy for resistant hypertension: a systematic review and meta-analysis. J Am Coll Cardiol. 2013;62:231-241.
Bocchi EA, Marcondes-Braga FG, Bacal F, et al. Updating of the Brazilian guideline for chronic heart failure - 2012. Arq Bras Cardiol. 2012;98:1-33.
Geng J, Chen C, Zhou X, Qian W, Shan Q. Influence of renal sympathetic denervation in patients with early-stage heart failure versus late-stage heart failure. Int Heart J. 2018;59:99-104.
Hasking GJ, Esler MD, Jennings GL, Burton D, Johns JA, Korner PI. Norepinephrine spillover to plasma in patients with congestive heart failure: evidence of increased overall and cardiorenal sympathetic nervous activity. Circulation. 1986;73:615-621.
Hasking GJ, Esler MD, Jennings GL, Dewar E, Lambert G. Norepinephrine spillover to plasma during steady-state supine bicycle exercise. Comparison of patients with congestive heart failure and normal subjects. Circulation. 1988;78:516-521.
Dzau VJ, Colucci WS, Hollenberg NK, Williams GH. Relation of the renin-angiotensin-aldosterone system to clinical state in congestive heart failure. Circulation. 1981;63:645-651.
Writing Committee M, Yancy CW, Jessup M, et al. 2016 ACC/AHA/HFSA focused update on new pharmacological therapy for heart failure: an update of the 2013 ACCF/AHA Guideline for the Management of Heart Failure: a report of the American College of Cardiology/American Heart Association task force on clinical practice guidelines and the Heart Failure Society of America. Circulation. 2016;134:e282.#x2010;e293.
Chuenkova MV, Pereiraperrin M. Enhancement of tyrosine hydroxylase expression and activity by Trypanosoma cruzi parasite-derived neurotrophic factor. Brain Res. 2006;1099:167-175.
Akpan N, Caradonna K, Chuenkova MV, PereiraPerrin M. Chagas' disease parasite-derived neurotrophic factor activates cholinergic gene expression in neuronal PC12 cells. Brain Res. 2008;1217:195-202.
Merejo Pena CM, Reis MS, Pereira BB, Nascimento EMD, Pedrosa RC. Dysautonomy in different death risk groups (Rassi score) in patients with Chagas heart disease. Pacing Clin Electrophysiol. 2018;41:238-245.
Bonfante-Cabarcas R, Lopez Hincapie E, Jimenez Hernandez E, et al. Electrophysiological and pharmacological evaluation of the nicotinic cholinergic system in chagasic rats. BMC Pharmacol Toxicol. 2013;14(2):1-9.
Beltrame SP, Auger SR, Bilder CR, Waldner CI, Goin JC. Modulation of M(2) muscarinic receptor-receptor interaction by immunoglobulin G antibodies from Chagas' disease patients. Clin Exp Immunol. 2011;164:170-179.
Marin-Neto JA, Simoes MV, Rassi Junior A. Pathogenesis of chronic Chagas cardiomyopathy: the role of coronary microvascular derangements. Rev Soc Bras Med Trop. 2013;46:536-541.

Auteurs

André G Spadaro (AG)

Heart Institute (InCor), University of São Paulo Medical School, São Paulo, São Paulo, Brazil.

Edimar A Bocchi (EA)

Heart Institute (InCor), University of São Paulo Medical School, São Paulo, São Paulo, Brazil.

Germano E Souza (GE)

Heart Institute (InCor), University of São Paulo Medical School, São Paulo, São Paulo, Brazil.

Antonio E Filho (AE)

Heart Institute (InCor), University of São Paulo Medical School, São Paulo, São Paulo, Brazil.

José Mariani (J)

Heart Institute (InCor), University of São Paulo Medical School, São Paulo, São Paulo, Brazil.
Hospital Israelita Albert Einstein, São Paulo, São Paulo, Brazil.

Carlos M Campos (CM)

Heart Institute (InCor), University of São Paulo Medical School, São Paulo, São Paulo, Brazil.
Hospital Israelita Albert Einstein, São Paulo, São Paulo, Brazil.

Pedro A Lemos (PA)

Heart Institute (InCor), University of São Paulo Medical School, São Paulo, São Paulo, Brazil.
Hospital Israelita Albert Einstein, São Paulo, São Paulo, Brazil.

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