Abstract
Purpose of Review
Chagas’ disease has become an emerging health problem due to increased migration. In the present review, we have summarized the usefulness of non-invasive imaging tools for the diagnosis of cardiac involvement in Chagas’ disease, with emphasis on modern technologies. M-mode, bidimensional (2-D), and three-dimensional (3-D) echocardiographies may allow the evaluation of left ventricular (LV) regional and global contractile function, right ventricle (RV) impairment, evidence of aneurysms and thrombi, and assessment of diastolic function in any stage of the disease.
Recent Findings
New modalities such as strain and speckle-tracking imaging have brought non-invasive indices to the understanding of the mechanisms of cardiac dyssynchrony. The assessment of cardiac autonomic denervation using 123I-metaiodobenzylguanidine (123I-MIBG), LV, and RV systolic function and the study of LV mechanical dyssynchrony by gated cardiac blood pool are available in current nuclear imaging for patients with Chagas’ disease. The findings of myocardial fibrosis by cardiac magnetic resonance (CMR), mainly in inferolateral regions, are a marker of subclinical involvement and worse prognosis in Chagas’ disease, even in patients with preserved ventricular function.
Summary
The detection and quantification of early signs of heart involvement by new technologies should be useful for risk stratification and in the clinical decision process for new therapeutic methods and could improve the natural history of the disease.
Similar content being viewed by others
References
Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance
Andrade JP, Marin Neto JA, Paola AMV, et al. I Latin American Guidelines for the diagnosis and treatment of Chagas’ heart disease: executive summary. Arq Bras Cardiol. 2010;96(6):434–42.
Rassi Jr A, Rassi A, Marin-Neto A. Chagas disease. Lancet. 2010;375:1388–402.
Marin-Neto JA, Cunha-Neto E, Maciel BC, Simões MV. Pathogenesis of chronic Chagas heart disease. Circulation. 2007;115:1109–23.
Higuchi ML, Benvenuti LA, Reis MM, Metzger M. Pathophysiology of the heart in Chagas’ disease: current status and new developments. Cardiovasc Res. 2003;60:96–107.
Rassi Jr A, Rassi A, Little WC, et al. Development and validation of a risk score for predicting death in Chagas’ heart disease. N Engl J Med. 2006;355(8):799–808.
• do C Rassi D, Vieira ML, Arruda AL, et al. Echocardiographic parameters and survival in Chagas heart disease with severe systolic dysfunction. Arq Bras Cardiol. 2014;102(3):245–52. In this multicenter randomized trial, indexed left atrial volume was the only predictor of mortality in patients with Chagas’ disease and severe systolic dysfunction.
Viotti RJ, Vigliano C, Laucella S, et al. Value of echocardiogram for diagnosis and prognosis of chronic chagasic myocarditis without heart failure. Heart. 2004;90:655–60.
Nunes MC, Barbosa MM, Ribeiro AL, Colosimo EA, Rocha MO. Left atrial volume provides independent prognostic value in patients with Chagas cardiomyopathy. J Am Soc Echocardiogr. 2009;22(1):82–8.
Barbosa MM, Costa Rocha MO, Vidigal DF, et al. Early detection of left ventricular contractility abnormalities by two-dimensional speckle tracking strain in Chagas’ disease. Echocardiography. 2014;31(5):623–30.
Lang RM, Badano LP, Mor-Avi V, et al. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr. 2015;28(1):1–39.
Lancellotti P, Tribouilloy C, Hagendorff A, et al. Scientific document committee of the European Association of Cardiovascular Imaging. Recommendations for the echocardiographic assessment of native valvular regurgitation: an executive summary from the European Association of Cardiovascular Imaging. Eur Heart J Cardiovasc Imaging. 2013;14:611–44.
Lang RM, Badano LP, Tsang W, et al. American Society of Echocardiography; European Association of Echocardiography. EAE/ASE recommendations for image acquisition and display using three-dimensional echocardiography. J Am Soc Echocardiogr. 2012;25:3–46.
Mancuso FJ, Almeida DR, Moisés VA, et al. Left atrial dysfunction in Chagas cardiomyopathy is more severe than in idiopathic dilated cardiomyopathy: a study with real-time three-dimensional echocardiography. J Am Soc Echocardiogr. 2011;24(5):526–32.
Tsang W, Salgo IS, Medvedofsky D, et al. Transthoracic 3D echocardiographic left heart chamber quantification using an automated adaptive analytics algorithm. J Am Coll Cardiol Cardiovasc Imaging. 2016;9(7):769–82.
Vieira ML, Oliveira WA, Cordovil A, et al. 3D Echo pilot study of geometric left ventricular changes after acute myocardial infarction. Arq Bras Cardiol. 2013;101(1):43–51.
Gimenes VM, Vieira ML, Andrade MM, et al. Standard values for real-time transthoracic three-dimensional echocardiographic dyssynchrony indexes in a normal population. J Am Soc Echocardiogr. 2008;21(11):1229–35.
Vieira ML, Cury AF, Gustavo N, et al. Ventricular dyssynchrony index: comparison with two-dimensional and three-dimensional ejection fraction. Arq Bras Cardiol. 2008;91(3):142–7. 156–62.
Hotta VT, Martinelli Filho M, Mady C, Mathias Jr W, Vieira ML. Comparison between 2D and 3D echocardiography in the evaluation of reverse remodeling after CRT. Arq Bras Cardiol. 2011;97(2):111–21.
Hotta VT, Martinelli Filho M, Mathias Jr W, Vieira ML. New equation for prediction of reverse remodeling after cardiac resynchronization therapy. Echocardiography. 2012;29(6):678–87.
• Stockburger M, Moss AJ, Klein HU, et al. Sustained clinical benefit of cardiac resynchronization therapy in non-LBBB patients with prolonged PR-interval: MADIT-CRT long-term follow-up. Clin Res Cardiol. 2016;105:944–52. In non-LBBB patients with prolonged PR-interval, CRT/ICD reduced the risk of heart failure or death (67%), compared to an ICD-only. These data could provide a guide to the treatment in patients with Chagas’ disease.
Hahn RT, Abraham T, Adams MS, et al. Guidelines for performing a comprehensive transesophageal echocardiographic examination: recommendations from the American Society of Echocardiography and the Society of Cardiovascular Anesthesiologists. J Am Soc Echocardiogr. 2013;26(9):921–64.
Morris SA, Tanowitz HB, Wittner M, Bilezikian JP. Pathophysiological insights into the cardiomyopathy of Chagas’ disease. Circulation. 1990;82(6):1900–9.
Nunes MC, Dones W, Morillo CA, Encina JJ, Ribeiro AL. Chagas disease: an overview of clinical and epidemiological aspects. J Am Coll Cardiol. 2013;62:767–76.
Hagar JM, Rahimtoola SH. Chagas’ heart disease in the United States. N Engl J Med. 1991;325(11):763–8.
Tsan MF. Mechanism of gallium-67 accumulation in inflammatory lesions. J Nucl Med. 1985;26(1):88–92.
Fiorelli AI, Stolf NA, Honorato R, et al. Later evolution after cardiac transplantation in Chagas’ disease. Transplant Proc. 2005;37(6):2793–8.
Bocchi EA, Kalil R, Bacal F, et al. Magnetic resonance imaging in chronic Chagas’ disease: correlation with endomyocardial biopsy findings and gallium-67 cardiac uptake. Echocardiography. 1998;15(3):279–88.
Botvinick E, O’Connell J, Badhwar N. Imaging synchrony. J Nucl Cardiol. 2009;16:846–8.
Mady C, Ianni BM, Arteaga E, et al. Relation between interstitial myocardial collagen and the degree of clinical impairment in Chagas’ disease. Am J Cardiol. 1999;84(3):354–6. A9.
Freitas HF, Chizzola PR, Paes AT, et al. Risk stratification in a Brazilian hospital-based cohort of 1220 outpatients with heart failure: role of Chagas’ heart disease. Int J Cardiol. 2005;102(2):239–47.
Marin-Neto JA, Marzullo P, Marcassa C, et al. Myocardial perfusion abnormalities in chronic Chagas’ disease as detected by thallium-201 scintigraphy. Am J Cardiol. 1992;69(8):780–4.
Peix A, García R, Sánchez J, et al. Myocardial perfusion imaging and cardiac involvement in the indeterminate phase of Chagas disease. Arq Bras Cardiol. 2013;100(2):114–7.
Rochitte CE, Oliveira PF, Andrade JM, et al. Myocardial delayed enhancement by magnetic resonance imaging in patients with Chagas’ disease: a marker of disease severity. J Am Coll Cardiol. 2005;46(8):1553–8.
Torres FW, Acquatella H, Condado JA, et al. Coronary vascular reactivity is abnormal in patients with Chagas’ heart disease. Am Heart J. 1995;129(5):995–1001.
Di Carli MF, Tobes MC, Mangner T, et al. Effects of cardiac sympathetic innervation on coronary blood flow. N Engl J Med. 1997;336:1208–15.
Sarabanda AV, Sosa E, Simões MV, et al. Ventricular tachycardia in Chagas’ disease: a comparison of clinical, angiographic, electrophysiologic and myocardial perfusion disturbances between patients presenting with either sustained or nonsustained forms. Int J Cardiol. 2005;102(1):9–19.
Simões MV, Pintya AO, Bromberg-Marin G, et al. Relation of regional sympathetic denervation and myocardial perfusion disturbance to wall motion impairment in Chagas’ cardiomyopathy. Am J Cardiol. 2000;86(9):975–81.
Duarte JO, Magalhaes LP, Santana OO, et al. Prevalence and prognostic value of ventricular dyssynchrony in Chagas cardiomyopathy. Arq Bras Cardiol. 2011;96(4):300–6.
•• Narula J, Gerson M, Thomas GS, Cerqueira MD, Jacobson AF. 123I-MIBG imaging for prediction of mortality and potentially fatal events in heart failure: the ADMIRE-HFX study. J Nucl Med. 2015;56:1011–8. Large trial demonstrating that 123 I-MIBG imaging added excellent prognostic utility to the baseline risk models in patients with heart failure.
Pereira FT, Rocha EA, Monteiro MP, et al. Clinical course after cardioverter-defibrillator implantation: chagasic versus ischemic patients. Arq Bras Cardiol. 2016;11. doi: 10.5935/abc.20160101.
Brandão SC, Giorgi MC, Vieira ML, et al. Cardiac sympathetic activity pre and post resynchronization therapy evaluated by 123I-MIBG myocardial scintigraphy. J Nucl Cardiol. 2007;14(6):852–9.
Brandão SC, Nishioka SA, Giorgi MC, et al. Cardiac resynchronization therapy evaluated by myocardial scintigraphy with 99mTc-MIBI: changes in left ventricular uptake, dyssynchrony, and function. Eur J Nucl Med Mol Imaging. 2009;36(6):986–96. doi:10.1007/s00259-008-1029-1.
Chen J, Garcia EV, Folks RD, et al. Onset of left ventricular mechanical contraction as determined by phase analysis of ECG-gated myocardial perfusion SPECT imaging: development of a diagnostic tool for assessment of cardiac mechanical dyssynchrony. J Nucl Cardiol. 2005;12:687–95.
Hundley WG, Bluemke DA, Finn JP, et al. ACCF/ACR/AHA/NASCI/SCMR 2010 expert consensus document on cardiovascular magnetic resonance. A report of the American College of Cardiology Foundation task force on expert consensus documents. Circulation. 2010;121:2462–508.
Rochitte CA, Nacif MS, Oliveira Jr AC, et al. Cardiac magnetic resonance in Chagas’ disease. Artif Organs. 2007;31:259–67.
• Falchetto EB, Costa SCS, Rochitte CE. Diagnostic challenges of Chagas cardiomyopathy and CMR imaging. Global Heart. 2015;10:181–7. The diagnostic role of CMR in Chagas’ disease and its implications are reviewed.
Tassi EM, Continentino MA, Nascimento EM, Pereira BB, Pedrosa RC. Relationship between fibrosis and ventricular arrhythmias in Chagas heart disease without ventricular dysfunction. Arq Bras Cardiol. 2014;102:456–64.
Wu KC, Weiss RG, Thiemann DR, et al. Late gadolinium enhancement by cardiovascular magnetic resonance heralds an adverse prognosis in nonischemic cardiomyopathy. J Am Coll Cardiol. 2008;51:2414–21.
Rodríguez-Zanella H, Meléndez-Ramirez G, Velázquez L, Meave A, Alexanderson E. ECG scores correlates with myocardial fibrosis assessed by magnetic resonance: a study in Chagas heart disease. Int J Cardiol. 2015;187:78–9.
Lee-Felker SA, Thomas M, Felker ER, et al. Value of cardiac MRI for evaluation of chronic Chagas disease cardiomyopathy. Clin Radiol. 2016;71:618.e1–7.
Regueiro A, Garcia-Alvarez A, Sitges M, et al. Myocardial involvement in Chagas disease: insights from cardiac magnetic resonance. Int J Cardiol. 2013;165:107–12.
Rassi Jr A, Rassi JG, Rassi A. Sudden death in Chagas’ disease. Arq Bras Cardiol. 2001;76:75–96.
Rassi Jr A, Rassi A, Rassi S. Predictors of mortality in chronic Chagas disease. A systematic review of observational studies. Circulation. 2007;115:1101–8.
Mello RP, Szarf G, Schvartzman PR, et al. Delayed enhancement cardiac magnetic resonance imaging can identify the risk of ventricular tachycardia in Chagas’ disease. Arq Bras Cardiol. 2012;98:421–30.
Hotez PJ, Dumonteil E, Woc-Colburn L, et al. Chagas disease: “The new HIV/AIDS of the Americas”. Plos Negl Trop Dis. 2012;6(5):e1498.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of Interest
Andréa M. Falcão, Maria Clementina Giorgi, Marcelo L. Campos Vieira, William A. Chalela, and Salvador Borges-Neto declare that they have no conflict of interest.
Human and Animal Rights and Informed Consent
All reported studies/experiments with human or animal subjects performed by the authors have been previously published and were in compliance with all applicable ethical standards (including the Helsinki Declaration and its amendments, institutional/national research committee standards, and international/national/institutional guidelines).
Additional information
This article is part of the Topical Collection on Metabolic Syndrome and Diabetes
Rights and permissions
About this article
Cite this article
Falcão, A.M., Giorgi, M.C., Vieira, M.L.C. et al. Chagas’ Disease: Update on Current Diagnosis. Curr Cardiovasc Imaging Rep 9, 33 (2016). https://doi.org/10.1007/s12410-016-9394-9
Published:
DOI: https://doi.org/10.1007/s12410-016-9394-9