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Prof. Abeer Ahmed Aboulazm :: Publications:

Title:
Serum BLyS and APRIL as possible indicators of disease activity in pediatric systemic lupus erythematosus and juvenile idiopathic arthritis
Authors: Gehan Gamal Elolemy a,*, Eman Abdelalem Baraka a, Soha Abdelhady Gendy b,Eman Ramadan Abdelgwad c, Abeer Ahmed Aboelazm d
Year: 2018
Keywords: Pediatric SLE; SLEDAI; JIA; JADAS-27; BLyS; APRIL
Journal: The Egyptian Rheumatologist
Volume: 36
Issue: Not Available
Pages: 93-99
Publisher: Elsevier
Local/International: International
Paper Link: Not Available
Full paper Abeer Ahmed Aboulazm _blys abril.pdf
Supplementary materials Not Available
Abstract:

Aim of the work: To assess serum levels of B lymphocyte stimulator (BLyS) and a proliferation- inducing ligand (APRIL) to determine their correlations with disease activity in pediatric systemic lupus erythematosus (pSLE) and juvenile idiopathic arthritis (JIA) patients. Patients and methods: Twenty-nine pSLE patients and 33 JIA patients were recruited. SLE disease activity was assessed using the systemic lupus erythematosus disease activity index (SLEDAI), while the juvenile arthritis 27 joint disease activity score (JADAS-27) was calculated for JIA patients. Serum samples were assayed for BLyS and APRIL by the enzyme linked immunosorbent assay (ELISA). Results: Serum BLyS and APRIL were elevated in both pSLE and JIA patients compared to controls. Serum BLyS levels correlated with both SLE and JIA disease activity (p=0.042, p = 0.019, respectively) whereas serum APRIL levels correlated positively with JADAS-27 and inversely with SLEDAI (p= 0.001, p= 0.02, respectively). Elevated serum BLyS and APRIL were significantly associated with a lower incidence of nephritis (p= 0.043, p= 0.016, respectively), while elevated serum APRIL significantly associated with negative anti-dsDNA in pSLE patients (p = 0.017). In JIA patients, both serum BLyS and APRIL were significantly associated with the presence of ANA (p= 0.008, p< 0.001, respectively), while high serum APRIL associated with the presence of RF (p= 0.035). APRIL and BLYS levels correlated with each other positively in JIA but inversely in pSLE patients. Conclusion: Serum BLyS showed elevated levels that correlated significantly with pSLE and JIA disease activity, accordingly anti-BLyS therapy might be of great benefit to offset disease flare. The inverse correlations observed between APRIL with both BLyS and disease activity in pSLE patients raises the possibility of being a down regulator of the disease process.

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