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Published on: December 19, 2013
Relationship between microvascular changes, autonomic denervation, and myocardial fibrosis in Chagas cardiomyopathy:
Gustavo Canavaci Barizon1, Marcus Vinicius Simões2, André Schmidt2
1Department of Computing and Mathematics, University of São Paulo, Av. Bandeirantes, 3900, Ribeirão Preto, SP, 14040-901, Brazil. gustavo.canavaci@usp.br.
Insights
Autonomic denervation, hypoperfusion, and fibrosis in Chagas cardiomyopathy are strongly correlated. Myocardial autonomic denervation may be a sensitive marker for cardiac involvement in Chagas disease.
Area of Science:
- Cardiology
- Medical Imaging
- Pathophysiology
Background:
- The interplay between microvasculopathy, autonomic denervation, and myocardial fibrosis in Chagas cardiomyopathy remains unclear.
- Understanding these relationships is crucial for diagnosing and managing the disease.
Purpose of the Study:
- To investigate the extent and distribution of myocardial hypoperfusion, autonomic denervation, and scarring in Chagas cardiomyopathy.
- To explore the correlation between these pathological features using advanced imaging techniques.
Main Methods:
- Utilized Iodine-123-metaiodobenzylguanidine (MIBG) SPECT, 99mTc-Sestamibi (MIBI) rest-stress SPECT, and gadolinium late enhancement MRI in 13 Chagas disease patients.
- Co-registered and quantified areas of denervation, hypoperfusion, and fibrosis using SPECT and MRI.
Main Results:
- Demonstrated a strong anatomic concordance between hypoperfusion, denervation, and fibrosis.
- Found a close association between myocardial denervation and stress-induced hypoperfusion.
Conclusions:
- Combined analysis of autonomic denervation, hypoperfusion, and scarring aids understanding of Chagas cardiomyopathy pathophysiology.
- Autonomic myocardial denervation may serve as a sensitive indicator of cardiac involvement in Chagas disease.
Background:
The relationship between microvasculopathy, autonomic denervation, and myocardial fibrosis, in Chagas cardiomyopathy is incompletely understood. The aim of this study was to explore the relative extent and anatomic distribution of myocardial hypoperfusion, autonomic denervation, and myocardial scarring using Single-Photon Emission Computerized Tomography (SPECT) imaging and Magnetic Resonance Imaging (MRI).
Methods:
Thirteen patients with Chagas disease all had Iodine-123-metaiodobenzylguanidine (MIBG) SPECT, 99mTc-Sestamibi (MIBI) rest-stress SPECT, and gadolinium late enhancement MRI imaging within a 2-month interval. The anatomic location and extent of denervation, of stress-induced hypoperfusion and fibrosis, were assessed through image co-registration and quantification of abnormal tissue areas as a percent of total myocardium.
Results:
The results showed a strong general anatomic concordance between areas of hypoperfusion, denervation, and fibrosis, suggesting that the three abnormal features may be correlated. Myocardial denervation was anatomically and quantitatively closely associated areas of stress hypoperfusion.
Conclusion:
Combined myocardial analysis of the extent and location of autonomic denervation, hypoperfusion, and scarring may allow for better understanding of the pathophysiology of Chagas cardiomyopathy. Autonomic myocardial denervation may be a more sensitive marker of cardiac involvement in Chagas Disease than finding by other imaging modalities.
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