Key result
Ventricular arrhythmias in early Chagas cardiomyopathy link to ~4-fold greater sympathetic denervation alongside increased fibrosis.
Why the study?
Sudden cardiac death can be the initial event in chronic Chagas cardiomyopathy, but guidelines lack recommendations for early implantable cardioverter-defibrillator placement, prompting evaluation of autonomic denervation, hypoperfusion, and fibrosis in early stages.
Does the extent of sympathetic denervation, myocardial hypoperfusion, and myocardial fibrosis correlate with the presence of ventricular arrhythmias in patients with early-stage chronic Chagas cardiomyopathy and preserved left ventricular function?
Cross-Sectional (n=29)
Blinded image analysis by two experienced observers
No
Does the extent of sympathetic denervation, myocardial hypoperfusion, and myocardial fibrosis correlate with the presence of ventricular arrhythmias in patients with early-stage chronic Chagas cardiomyopathy and preserved left ventricular function?
In patients with early-stage chronic Chagas cardiomyopathy and preserved left ventricular function, sympathetic denervation, myocardial hypoperfusion, and myocardial fibrosis are significantly associated with ventricular arrhythmias, offering potential parameters to improve sudden cardiac death risk stratification.
May support imaging for arrhythmia risk stratification in early Chagas cardiomyopathy; leaves open prospective validation.
Background: Chronic Chagas cardiomyopathy (CCC) manifests as heart failure, thromboembolic events, and sudden cardiac death (SCD).Although SCD may be the presenting event, there is still no recommendation for early cardioverter/ defibrillator implantation in current guidelines.Objective: To evaluate the correlation between autonomic denervation, myocardial hypoperfusion, fibrosis, and ventricular arrhythmias in patients in the early stages of CCC.Methods: Cross-sectional study of 29 patients with CCC and preserved left ventricular function who underwent SPECT with iodine-123-meta-iodobenzylguanidine ( 123 I-mIBG), myocardial perfusion SPECT with technetium-99m sestamibi ( 99m Tc-MIBI), and cardiac magnetic resonance (CMR) with gadolinium, divided into two groups according to on 24h Holter findings: arrhythmia (> 6 ventricular premature complexes/hour and/or nonsustained ventricular tachycardia; n = 15) or no-arrhythmia (< 6 ventricular premature complexes/hour and no ventricular tachycardia; n = 14).Results: Significant correlations were observed between parameters of the three cardiovascular imaging modalities and the presence of ventricular arrhythmia.Denervation on mIBG correlated moderately with diffuse fibrosis, represented by ECV on CMR (r = 0.55, P = 0.002).Hypoperfusion by MIBI-SPECT correlated with fibrosis by both LGE (r = 0.66, P = 0.005) and extracelluar volume (ECV) (r = 0.56, P = 0.002).We also observed a moderate correlation between the extent of myocardial areas with denervation and hypoperfusion (r = 0.48, P = 0.007).Conclusion: The presence of autonomic denervation, myocardial hypoperfusion, and fibrosis was associated with ventricular arrhythmia in the early stages of CCC.A combination of these parameters can improve stratification of SCD risk in these patients.
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Brito et al. (2024) conducted a cross-sectional in Early-stage chronic Chagas cardiomyopathy with preserved left ventricular function (n=29). Ventricular arrhythmia (> 6 ventricular premature complexes/hour and/or nonsustained ventricular tachycardia on 24h Holter) vs. No ventricular arrhythmia (< 6 ventricular premature complexes/hour and no ventricular tachycardia on 24h Holter) was evaluated on Sympathetic denervation (123I-mIBG summed score), myocardial hypoperfusion (99mTc-MIBI TPD %), and myocardial fibrosis (CMR LGE %) (p=<0.01). Ventricular arrhythmias in early-stage chronic Chagas cardiomyopathy associated with greater sympathetic denervation (score 23.2 vs 5.6, p<0.01), hypoperfusion (p=0.01), and fibrosis (14.3% vs 4.0%, p=0.04).
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