Key result
Myocardial extracellular volume was independently associated with non-sustained ventricular tachycardia in early-stage Chagas disease (OR 1.80), even after adjusting for fibrosis mass and LVEF.
Why the study?
Chronic Chagas disease can lead to myocardial fibrosis and ventricular arrhythmia, prompting evaluation of CMR fibrosis parameters' associations with non-sustained ventricular tachycardia.
Does myocardial extracellular volume (ECV) assessed by CMR associate with non-sustained ventricular tachycardia in patients with early-stage Chagas disease?
Cross-Sectional (n=62)
Single-blind
No
Does myocardial extracellular volume (ECV) assessed by CMR associate with non-sustained ventricular tachycardia in patients with early-stage Chagas disease?
Myocardial extracellular volume assessed by CMR is independently associated with non-sustained ventricular tachycardia in early-stage Chagas cardiomyopathy, suggesting its potential as an early risk marker for ventricular arrhythmias.
Supports ECV as potential early NSVT risk marker in Chagas; hypothesis-generating and requires prospective validation before practice change.
Chronic Chagas disease can progress to myocardial involvement with intense fibrosis, which may predispose patients to sudden cardiac death through ventricular arrhythmia. The associations of myocardial fibrosis detected by cardiac magnetic resonance (CMR) parameters with non-sustained ventricular tachycardia (NSVT) were evaluated. This cross-sectional study included patients in early stages of Chagas disease (n = 47) and a control group (n = 15). Patients underwent cardiac evaluation, including CMR examination. Myocardial fibrosis assessment by CMR with measurement of late gadolinium enhancement (LGE), native T1, and extracellular volume (ECV) was performed. There was an increase in myocardial fibrosis CMR parameters and ventricular arrhythmias among different stages of Chagas disease, combined with a decrease in the left ventricular ejection fraction (LVEF) by CMR and also in the right ventricular systolic function by S’ wave on tissue Doppler. Fibrosis mass and ECV were associated with the Rassi score, ventricular extrasystole, and E/e’ ratio in a logistic regression model adjusted for age and gender. The ECV maintained an association with the presence of NSVT, even after adjustments for fibrosis mass and LVEF assessed by CMR. The receiver-operating characteristic area under the curve for global ECV (0.85; 95% CI: 0.71–0.99) and NSVT was greater than that for fibrosis mass (0.75; 95% CI: 0.54–0.96), although this difference was not statistically significant. Extracellular volume could be an early marker of increased risk of ventricular arrhythmia in Chagas disease, presenting an independent association with NSVT in the initial stages of chronic Chagas cardiomyopathy, even after adjustment for fibrosis mass and LVEF.
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Pinheiro et al. (2020) conducted a cross-sectional in Chagas disease (n=62). Myocardial extracellular volume (ECV) vs. Unexposed/lower ECV was evaluated on Presence of non-sustained ventricular tachycardia (NSVT) (OR 1.80, 95% CI 1.13-2.87, p=0.01). Myocardial extracellular volume was independently associated with non-sustained ventricular tachycardia in early-stage Chagas disease (OR 1.80), even after adjusting for fibrosis mass and LVEF.
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