Key result
Lower serum Thymosin β4 is linked to Kawasaki disease, with further drops in coronary lesions.
Why the study?
The role of thymosin β4 in Kawasaki disease and its relationship to inflammation and coronary artery lesions remains poorly understood.
Are serum Thymosin β4 levels associated with coronary arterial lesions and inflammation in children with Kawasaki disease?
Observational (n=145)
No
Are serum Thymosin β4 levels associated with coronary arterial lesions and inflammation in children with Kawasaki disease?
Serum Thymosin β4 levels are significantly reduced in children with Kawasaki disease, particularly those with coronary arterial lesions, suggesting a potential role in its inflammatory pathogenesis.
Background: Kawasaki disease (KD) is an acute systemic vasculitis primarily affecting children and is a leading cause of acquired heart disease in developed countries. Recently, an increasing number of studies have demonstrated the close correlations between inflammation and KD. Thymosin β4 (Tβ4) has been reported to play a role in cardiovascular protection and repair by modulating inflammation, angiogenesis, and endothelial function. However, its role in KD still remains poorly understood. This study aims to explore the potential involvement of Tβ4 in the pathogenesis of KD, with a particular focus on its relationship to inflammation and coronary artery lesions (CALs). Methods: Serum Tβ4 levels were measured using enzyme-linked immunosorbent assay (ELISA) in children with KD and age-matched healthy controls. The KD group was further categorized into patients with and without CALs. Correlation analyses were performed between Tβ4 levels and clinical or laboratory parameters. Results: Serum Tβ4 levels were significantly lower in patients with KD compared to healthy controls and were further reduced in patients with CALs. After intravenous immunoglobulin (IVIG) treatment, Tβ4 levels significantly increased. Tβ4 levels were negatively correlated with several pro-inflammatory (eg, TNF-α, IL-1β) and anti-inflammatory cytokines (eg, IL-4, IL-10). Conclusion: Tβ4 levels were significantly lower in children with KD, particularly in those with CALs. These findings suggest that Tβ4 may be involved in the inflammatory pathogenesis of KD and the progression of CALs, thus could represent a potential target for future diagnostic or therapeutic interventions.
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Wu et al. (2025) conducted an observational in Kawasaki disease (n=145). Kawasaki disease vs. Healthy controls was evaluated on Serum Thymosin β4 levels (mg/mL) (p=<0.05). Serum Thymosin β4 levels were significantly lower in children with Kawasaki disease compared to healthy controls (median 0.903 vs 1.190 mg/mL) and were further reduced in those with coronary artery lesions.
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