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Cytokine Profiles and Inflammatory Implications in Chagas Disease: Associations with Ventricular Function and
Mario Principato1, Maria Victoria Carvelli1, Analia Gladys Paolucci1
1Cardiology Division, Hospital General de Agudos José María Ramos Mejía, Buenos Aires C1221ADC, Argentina.
Insights
Specific cytokines are linked to conduction problems in Chagas cardiomyopathy patients with preserved ejection fraction. Further research is needed to confirm their prognostic and therapeutic roles.
Area of Science:
- Cardiology
- Immunology
- Infectious Diseases
Background:
- Chagas cardiomyopathy (CC) pathogenesis involves cytokines and chemokines, but their role in conduction disturbances and left ventricular ejection fraction (LVEF) is unclear.
- Understanding these roles is crucial for managing CC progression and patient outcomes.
Purpose of the Study:
- To investigate associations between cytokine levels and systolic function in Chagas disease patients.
- To compare cytokine levels between patients with preserved and reduced LVEF.
- To examine cytokine differences within the preserved LVEF group based on the presence of conduction disturbances.
Main Methods:
- An analytical cross-sectional study included Chagas disease patients (divided by LVEF: >50% and <35%) and healthy controls.
- Cytokine levels (IFN-γ, IL-1β, IL-6, IL-10, IL-12p70, IL-15, IL-17A, MCP-1, MIP1α, TNF-α, IL-2) were measured using a multiplex assay.
- Patients with preserved LVEF were further analyzed based on the presence or absence of intraventricular conduction disturbances.
Main Results:
- No significant cytokine differences were found between Chagas disease patients with preserved versus reduced LVEF.
- Within the preserved LVEF group, patients with conduction disturbances showed elevated levels of IL-10, IL-12p70, IL-2, IL-15, MIP1α, and IFN-γ compared to those without.
- Chagas disease patients with preserved LVEF and no conduction issues had cytokine profiles similar to healthy controls.
Conclusions:
- Elevated levels of specific cytokines correlate with conduction disturbances in Chagas disease patients with preserved LVEF.
- A causal link between these cytokines and conduction disturbances requires further investigation.
- Future research should explore the prognostic and therapeutic implications of these cytokine findings in Chagas cardiomyopathy.
Background:
The roles of cytokines and chemokines in the pathogenesis of Chagas cardiomyopathy (CC) have been proposed, yet their clinical significance with respect to conduction disturbances and left ventricular ejection fraction (LVEF) remains unclear.
Aim:
The objective of this study was to analyze the associations between cytokine levels and systolic function, comparing patients with preserved and reduced ejection fractions. As a secondary objective, we evaluated whether differences were present in cytokine levels within the subgroup with preserved ejection fraction, depending on the presence or absence of intraventricular conduction disturbances.
Methods:
We conducted an analytical cross-sectional study involving patients with Chagas disease and a healthy control group. Among patients with Chagas disease, those with preserved (>50%) and reduced (<35%) left ventricular ejection fraction (LVEF) were selected. The preserved-LVEF group included individuals with and without conduction disorders. Cytokines (IFN-γ, IL-1β, IL-6, IL-10, IL-12p70, IL-15, IL-17A, MCP-1, MIP1α, TNF-α, and IL-2) were quantified using a magnetic bead-based multiplex assay.
Results:
Forty-four patients with CD (26 men, 59%) and 14 seronegative controls were included. In the CD group, 50% (n = 22) had preserved LVEF (LVEF > 50%), and 50% (n = 22) had decreased LVEF (≤35%). No significant differences in cytokine concentrations were observed between patients with preserved and reduced LVEF for TNF-α (19.74 ± 8.32 vs. 22.23 ± 6.40 pg/mL; p = 0.189), IL-6 (2.17 ± 2.41 vs. 5.40 ± 6.40 pg/mL; p = 0.145), IL-2 (2.61 ± 1.05 vs. 2.97 ± 1.79 pg/mL; p = 0.481), MCP-1 (214.18 ± 96.99 vs. 183.83 ± 63.21 pg/mL; p = 0.481) and IFN-γ (9.04 ± 4.90 vs. 7.64 ± 3.78 pg/mL; p = 0.372). Within the subgroup with preserved LVEF (n = 22), those with conduction disorders (n = 10) exhibited higher levels of IL-10 (24.49 vs. 9.83 pg/mL; q = 0.009), IL-12p70 (13.20 vs. 9.02 pg/mL; q = 0.027), IL-2 (2.70 vs. 2.07 pg/mL; q = 0.023), IL-15 (7.09 vs. 3.36 pg/mL; q = 0.018), MIP1α (10.33 vs. 3.35 pg/mL; q = 0.014) and IFN-γ (10.83 vs. 7.25 pg/mL; q = 0.005), compared to those without conduction disorders (n = 12). Notably, patients with CD and preserved LVEF (>50%) without conduction disturbances presented cytokine profiles similar to those of seronegative healthy controls with LVEF ≥ 50%.
Conclusions:
Elevated levels of specific cytokines were associated with conduction disturbances in patients with preserved LVEF. Despite this finding, a causal relationship cannot be established, and future studies are needed to explore their prognostic or therapeutic significance.
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