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Updated: Jun 24, 2026

In Vivo Quantitative Assessment of Myocardial Structure, Function, Perfusion and Viability Using Cardiac Micro-computed Tomography
Published on: February 16, 2016
Changes in myocardial perfusion correlate with deterioration of left ventricular systolic function in chronic Chagas'
Flávio C Hiss1, Thiago F Lascala, Benedito C Maciel
1Division of Cardiology, University Hospital, Medical School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Insights
Myocardial perfusion defects in chronic Chagas
Area of Science:
- Cardiology
- Nuclear Medicine
- Cardiovascular Imaging
Background:
- Coronary microvascular dysfunction and myocardial perfusion disturbances are implicated in the pathogenesis of Chagas' cardiomyopathy (CCC).
- Understanding these mechanisms is crucial for managing myocardial damage in CCC patients.
Purpose of the Study:
- To analyze the association between myocardial perfusion changes and the progression of left ventricular systolic dysfunction in patients with chronic Chagas' cardiomyopathy (CCC).
Main Methods:
- Prospective evaluation of 36 CCC patients (mean age 57 years) after 5.6 years.
- Quantification of stress and rest myocardial perfusion defects using single-positron emission computed tomography (SPECT) and polar maps.
- Assessment of left ventricular ejection fraction and systolic function via 2-dimensional echocardiography.
Main Results:
- Significant reduction in left ventricular ejection fraction and increase in rest perfusion defect area observed over time.
- Increased rest perfusion defect area strongly correlated with reduced left ventricular ejection fraction.
- Reversible perfusion defects progressed to rest defects in 68% of segments, indicating disease progression.
Conclusions:
- Progression of left ventricular systolic dysfunction in CCC is linked to reversible and increasing rest myocardial perfusion defects.
- Myocardial perfusion disturbances play a significant role in the pathogenesis of myocardial injury in chronic Chagas' cardiomyopathy.
- SPECT imaging can identify perfusion abnormalities that predict disease progression in CCC.
Objectives:
This study aimed at analyzing the association between myocardial perfusion changes and the progression of left ventricular systolic dysfunction in patients with chronic Chagas' cardiomyopathy (CCC).
Background:
Pathological and experimental studies have suggested that coronary microvascular derangement, and consequent myocardial perfusion disturbance, may cause myocardial damage in CCC.
Methods:
Patients with CCC (n = 36, ages 57 +/- 10 years, 17 males), previously having undergone myocardial perfusion single-positron emission computed tomography and 2-dimensional echocardiography, prospectively underwent a new evaluation after an interval of 5.6 +/- 1.5 years. Stress and rest myocardial perfusion defects were quantified using polar maps and normal database comparison.
Results:
Between the first and final evaluations, a significant reduction of left ventricular ejection fraction was observed (55 +/- 11% and 50 +/- 13%, respectively; p = 0.0001), as well as an increase in the area of the perfusion defect at rest (18.8 +/- 14.1% and 26.5 +/- 19.1%, respectively; p = 0.0075). The individual increase in the perfusion defect area at rest was significantly correlated with the reduction in left ventricular ejection fraction (R = 0.4211, p = 0.0105). Twenty patients with normal coronary arteries (56%) showed reversible perfusion defects involving 10.2 +/- 9.7% of the left ventricle. A significant topographic correlation was found between reversible defects and the appearance of new rest perfusion defects at the final evaluation. Of the 47 segments presenting reversible perfusion defects in the initial study, 32 (68%) progressed to perfusion defects at rest, and of the 469 segments not showing reversibility in the initial study, only 41 (8.7%) had the same progression (p < 0.0001, Fisher exact test).
Conclusions:
In CCC patients, the progression of left ventricular systolic dysfunction was associated with both the presence of reversible perfusion defects and the increase in perfusion defects at rest. These results support the notion that myocardial perfusion disturbances participate in the pathogenesis of myocardial injury in CCC.
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