Increased concentrations of IL-18 and uric acid in sickle cell anemia: Contribution of hemolysis, endothelial activation and the inflammasome

► We observed a positive correlation between IL-18 and uric acid. ► Classical markers of prognosis were associated with IL-18 and uric acid. ► The inflammasome probably contributes or influences vascular events in SCA. ► We suggest the IL-18 and uric acid as important biomarkers in monitoring SCA pa...

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Veröffentlicht in:Cytokine (Philadelphia, Pa.) Pa.), 2011-11, Vol.56 (2), p.471-476
Hauptverfasser: Cerqueira, Bruno A.V., Boas, Wendell V., Zanette, Angela D., Reis, Mitermayer G., Goncalves, Marilda S.
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Sprache:eng
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Zusammenfassung:► We observed a positive correlation between IL-18 and uric acid. ► Classical markers of prognosis were associated with IL-18 and uric acid. ► The inflammasome probably contributes or influences vascular events in SCA. ► We suggest the IL-18 and uric acid as important biomarkers in monitoring SCA patients. Sickle cell anemia (SCA) is a common, severe monogenetic disorder characterized by chronic hemolysis, frequent infections, a chronic inflammatory state and recurrent occlusions of the microcirculation, resulting in painful crises, organ damage and premature death. This study evaluated associations between serum levels of IL-18, uric acid, hemolytic markers, and inflammatory molecules in SCA patients. A cross-sectional study was performed including 45 SCA patients (median age of 20.5years) without general symptoms and who had not undergone blood transfusions. Inclusion criteria for the steady-state SCA patients were the absence of hospitalization and the absence of infections. Interleukin-18 and uric acid levels were correlated closely with markers of hemolysis, endothelial dysfunction and others cytokines levels. These findings suggest probable influences of IL-18 and uric acid in the pathophysiology of vascular occlusion in SCA. Additional studies should be performed to characterize similar prognosis markers and possible therapeutic targets.
ISSN:1043-4666
1096-0023
DOI:10.1016/j.cyto.2011.08.013