# Serum cytokines and tissue doppler imaging as markers of prognosis of chronic myocarditis due to chagas disease

**Authors:** Ivan Santana Batista Soares, Edmundo Câmara, Manoel Barral-Netto, Carlos Rico Quintero, Benelson Guimarães Carvalho, Fábio Bulhões, Alex Cleber Improta-Caria, Roque Aras-Júnior

PMC · DOI: 10.1016/j.bjid.2026.105786 · The Brazilian Journal of Infectious Diseases · 2026-02-21

## TL;DR

This study identifies specific cytokines and tissue Doppler imaging as potential early indicators of heart problems in people with Chagas disease.

## Contribution

The study identifies IL-5, IL1-B, and IL-13 as early independent predictors of adverse outcomes in Chagas disease.

## Key findings

- IL1-B and IL-13 were significantly associated with primary and total events in Chagas disease patients.
- Tissue Doppler imaging variables showed significant associations with primary outcomes.
- IL-5 independently predicted total events in adjusted analyses.

## Abstract

Insidious myocarditis due to Chagas disease evolves with low inflammatory potential. Determining biomarkers can help find individuals at risk for Heart Failure (HF) or arrhythmias. This study aimed to evaluate the role of serum cytokines and myocardial tissue Doppler imaging as prognostic markers of Chagas myocarditis.

This longitudinal study was carried out in a prospective cohort in which adults living with Chagas disease who had no HF were followed up for 10-years. Tissue Doppler imaging was performed, and inflammatory cytokines were measured. Kaplan-Meier survival analysis, unadjusted and adjusted survival analyses for some variables by Cox regression and multivariate binary logistic regression analysis were performed for the primary and total outcomes.

This study found that IL1-B and IL-13 were associated with primary and total events (p = 0.015 and p = 0.013 and p = 0.013 and 0.042, respectively). In the adjusted analysis, IL1-B and IL-13 remained associated with primary events, with p = 0.027 and p = 0.030, respectively, and IL1-B with total events (p = 0.022). In the logistic regression analysis, IL-5 independently predicted total events (p = 0.023). We found a significant association between tissue Doppler imaging variables and primary outcomes.

Identifying IL-5, IL1-B and IL-13 as probable independent predictors of events at an early stage of Chagas disease is a significant milestone to the understanding of this pathology evolution. Also, several tissue Doppler parameters were important as prognosis predictors.

## Linked entities

- **Proteins:** IL1B (interleukin 1 beta), IL13 (interleukin 13), IL5 (interleukin 5)
- **Diseases:** Chagas disease (MONDO:0001444), Heart Failure (MONDO:0005252)

## Full-text entities

- **Genes:** CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CSF3 (colony stimulating factor 3) [NCBI Gene 1440] {aka C17orf33, CSF3OS, GCSF}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL7 (interleukin 7) [NCBI Gene 3574] {aka IL-7, IMD130}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, CCL4 (C-C motif chemokine ligand 4) [NCBI Gene 6351] {aka ACT2, AT744.1, G-26, HC21, LAG-1, LAG1}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}
- **Diseases:** diastolic dysfunction (MESH:D018487), ventricular dilation (MESH:C566255), arrhythmia (MESH:D001145), myocardial lesions (MESH:D009059), Obesity (MESH:D009765), cardiomyopathy (MESH:D009202), myocarditis (MESH:D009205), arrhythmic (OMIM:212500), intraventricular branch blocks (MESH:D006345), chronic inflammation (MESH:D007249), left anterior fascicular block (MESH:D002037), ventricular dysfunction (MESH:D018754), type 2 diabetes mellitus (MESH:D003924), HF (MESH:D006333), Chagas cardiomyopathy (MESH:D002598), thromboembolism (MESH:D013923), coronary artery disease (MESH:D003324), heart condition (MESH:D006331), clinical (MESH:D000075902), CD (MESH:D014355), ventricular tachycardia (MESH:D017180), tissue damage (MESH:D017695), hypertension (MESH:D006973), death (MESH:D003643), sudden death (MESH:D003645), heart chamber dilation (MESH:D002311), infected (MESH:D007239), atrial fibrillation (MESH:D001281), atrioventricular blocks (MESH:D054537)
- **Chemicals:** benznidazole (MESH:C009999), ACEI (-), CB (MESH:C063451)
- **Species:** Trypanosoma cruzi (species) [taxon 5693], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937158/full.md

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Source: https://tomesphere.com/paper/PMC12937158