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An Intact Pericardium Ischemic Rodent Model
Published on: September 2, 2021
Cytokines in pericardial effusion of patients with inflammatory pericardial disease
Konstantinos Karatolios1, Rainer Moosdorf, Bernhard Maisch
1Department of Cardiology, University Hospital Giessen & Marburg, 35043 Marburg, Germany. karatoli@med.uni-marburg.de
Insights
Vascular Endothelial Growth Factor (VEGF) and basic Fibroblast Growth Factor (bFGF) are elevated in inflammatory pericardial effusion, suggesting their involvement in the disease's development. These angiogenic cytokines play a key role in inflammatory heart conditions.
Area of Science:
- Cardiology
- Biochemistry
- Immunology
Background:
- The specific roles of inflammatory and angiogenic cytokines in inflammatory pericardial effusion (PE) are not fully understood.
- Investigating these cytokines is crucial for understanding the pathogenesis of inflammatory heart conditions.
Purpose of the Study:
- To assess and compare the levels of vascular Endothelial Growth Factor (VEGF), basic Fibroblast Growth Factor (bFGF), Interleukin-1 beta (IL-1β), and Tumor Necrosis Factor-alpha (TNF-α) in pericardial effusion and serum.
- To determine the relationship between these cytokines and the causes of inflammatory PE (autoreactive vs. viral) and coronary artery disease (CAD).
Main Methods:
- Enzyme-linked immunosorbent assay (ELISA) was used to measure cytokine levels.
- Samples were collected from patients with inflammatory PE (autoreactive and viral) and control patients with CAD.
- Cytokine levels in pericardial fluid (PF) and serum were analyzed.
Main Results:
- VEGF levels were significantly higher in both PE and serum of patients with inflammatory PE compared to CAD patients.
- Pericardial bFGF levels were higher than serum levels in both inflammatory PE and CAD groups.
- Pericardial VEGF correlated positively with inflammation markers, while bFGF showed a negative correlation. IL-1β and TNF-α were rarely detected.
Conclusions:
- Elevated levels of VEGF and bFGF in pericardial effusion indicate their potential involvement in the pathogenesis of inflammatory pericardial disease.
- These findings highlight the importance of angiogenic cytokines in inflammatory cardiovascular conditions.
Background:
The role of inflammatory and angiogenic cytokines in patients with inflammatory pericardial effusion still remains uncertain.
Methods:
We assessed pericardial and serum levels of VEGF, bFGF, IL-1β and TNF-α by ELISA in patients with inflammatory pericardial effusion (PE) of autoreactive (n = 22) and viral (n = 11) origin, and for control in pericardial fluid (PF) and serum (n = 26) of patients with coronary artery disease (CAD) undergoing coronary artery bypass graft surgery.
Results:
VEGF levels were significantly higher in patients with autoreactive and viral PE than in patients with CAD in both PE (P = 0.006 for autoreactive and P < 0.001 for viral PE) and serum (P < 0.001 for autoreactive and P < 0.001 for viral PE). Pericardial bFGF levels were higher compared to serum levels in patients with inflammatory PE and patients with CAD (P ≤ 0.001 for CAD; P ≤ 0.001 for autoreactive PE; P = 0, 005 for viral PE). Pericardial VEGF levels correlated positively with markers of pericardial inflammation, whereas pericardial bFGF levels showed a negative correlation. IL-1β and TNF-α were detectable only in few PE and serum samples.
Conclusions:
VEGF and bFGF levels in pericardial effusion are elevated in patients with inflammatory PE. It is thus possible that VEGF and bFGF participate in the pathogenesis of inflammatory pericardial disease.
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