. 2012;60(3).
Pleural effusion complicates community-acquired pneumonia (CAP). It is thought that it is due to increased vascular permeability. Vascular endothelial growth factor (VEGF) is a cytokine with an important role in angiogenesis and vascular permeability. A suggested active role for VEGF in development of pleural effusion has been postulated. This study investigated serum levels of VEGF in hospitalized pediatric patients with CAP with and without pleural effusion. Forty-one cases with CAP were enrolled in the study against 40 age- and sex- matched healthy controls. The following investigations were performed: complete blood counts, chest x- ray, quantitative C-reactive protein, erythrocytic sedimentation rate and assay of serum VEGF. Patients with effusion were significantly older (p = 0.001), and their ESR, CRP and total leucocytic levels were significantly higher (p = 0.006, 0.007 and 0.004, respectively). Serum VEGF was significantly higher in cases when compared to controls (1060.29 ± 67 vs. 686.11 ± 50 pg/ml respectively, 95% CI= [111; 638], p = 0.006). Serum VEGF was significantly higher in cases with effusion when compared to cases without effusion (1329 ± 66 vs. 829 ± 60 pg/ml respectively, 95% CI= [95; 905], p = 0.017). There was a significant direct correlation between serum VEGF and pleural effusion (Spearman’s rho = 0.492, p = 0.001). The study concluded that there were elevated serum VEGF levels in children with CAP especially when associated with pleural effusion, and that the significant positive correlation between serum VEGF and amount of effusion postulate that VEGF, a potent inducer of vascular permeability, plays a causal role in pleural fluid formation.
Key words: Pneumonia, effusion, VEGF, children