Urinary excretion of IL-1β, IL-6 and IL-8 cytokines during relapse and remission of idiopathic nephrotic syndrome

• Main Authors: Al-Eisa AA, Al Rushood M, Al-Attiyah RJ
• Format: Article
• Language: English
• Published: Dove Medical Press 2017-01-01
• Series: Journal of Inflammation Research
• Subjects: Cytokine; IL1β; IL6; IL8; Idiopathic Nephrotic Syndrome; relapse.
• Online Access: https://www.dovepress.com/urinary-excretion-of-il-1beta-il-6-and-il-8-cytokines-during-relapse-a-peer-reviewed-article-JIR

Amal A Al-Eisa,1 Maysoun Al Rushood,1 Rajaa J Al-Attiyah2 1Department of Pediatrics, 2Department of Microbiology, Faculty of Medicine, Kuwait University, Safat, Kuwait Background/aim: The role of pro-inflammatory cytokines in the immunopathogenesis of idiopathic nephrotic syndrome had been widely postulated. Reports on the release of cytokines, during idiopathic nephrotic syndrome (INS) activation, were conflicting in defining a specific interleukin pattern during relapse and remission of the disease. The aim of this study was to explore the role of IL-1β, IL-6 and IL-8 in the pathophysiology of INS during relapse and remission.Patients and methods: A total of 37 INS patients were included. Their demographic and biochemical data were reviewed. Levels of IL-1β, IL-6 and IL-8 were measured in the urine of patients during relapse and remission of the disease. Urine samples from 30 age- and sex-matched controls were checked for the same 3 cytokines.Results: Mean age of patients at study was 6.4 ± 3.2 years (range: 14 months–12 years). Male:female ratio was 24:13. Mean serum creatinine was 47 ± 13 µmol/L, and mean serum albumin was 21 ± 7 g/L. Mean urinary IL-1β, IL-6 and IL-8 levels, corrected to urinary creatinine, in patients during relapse were 132.94 ± 654.97, 217.82 ± 1124.31 and 150.227 ± 523.97 pg/µmol compared to 9.11 ± 40.75, 0.146 ± 0.652, and 6.455 ± 24.53  pg/µmol in controls, respectively (P = 0.02, 0.03 and 0.014, respectively). No significant difference was reported in the mean level of the 3 cytokines compared to controls during remission (P = 0.94, 0.092 and 0.076).Conclusion: Our results support the role of T-cell activation and the subsequent release of IL-1β, IL6 and IL8 in the pathogenesis of relapses in INS. The use of steroid-sparing cytokine blockers in managing relapses of INS remains a tempting challenge. Keywords: cytokine, IL-1β, IL6, IL8, idiopathic nephrotic syndrome, relapse