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Correlation of plasma interleukin-18 concentration and severity of renal involvement and disease activity in systemic lupus erythematosus

Background: Systemic lupus erythematosus (SLE) is a systemic autoimmune disease characterized by activation of T and polyclonal B lymphocytes. IL-18 was originally identified as a factor which enhances IFN-γ production and is a potent inducer of the inflammatory mediators by T cells, causing severe...

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Autores principales: Jafari-Nakhjavani, Mohammad Reza, Abedi-Azar, Sima, Nejati, Babak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Diabetic Nephropathy Prevention 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4790184/
https://www.ncbi.nlm.nih.gov/pubmed/27047807
http://dx.doi.org/10.15171/jnp.2016.05
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author Jafari-Nakhjavani, Mohammad Reza
Abedi-Azar, Sima
Nejati, Babak
author_facet Jafari-Nakhjavani, Mohammad Reza
Abedi-Azar, Sima
Nejati, Babak
author_sort Jafari-Nakhjavani, Mohammad Reza
collection PubMed
description Background: Systemic lupus erythematosus (SLE) is a systemic autoimmune disease characterized by activation of T and polyclonal B lymphocytes. IL-18 was originally identified as a factor which enhances IFN-γ production and is a potent inducer of the inflammatory mediators by T cells, causing severe inflammatory disorders in SLE. Objectives: This study aimed to evaluate the association of plasma interlukine-18 (IL-18) concentration and severity of lupus nephritis (LN) and disease activity in SLE patients. Patients and Methods: In this cross-sectional study, 113 patients with SLE and 50 healthy individuals were examined. Serum level of IL-18 was measured. The severity and activity of the disease was determined by Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) score. The severity of kidney involvement was studied by renal biopsy, serum creatinine and 24 hours urine protein level. Results: The mean level of serum IL-18 was significantly higher in the patients than controls (577.67 ± 649.95 versus 60.48 ± 19.53 pg/ml; P < 0.001). In SLE patients with active disease level of serum IL-18 was significantly higher than chronic disease (622.77 ± 716.54 versus 182 ± 184.37 pg/ml; P < 0.001). The serum level of IL-18 was significantly higher in stage IV (P < 0.001) and V (P < 0.001) of patients with LN, than other stages. Conclusions: The current study showed that the serum IL-18 is significantly higher in the patients than controls and it significantly correlated with sever renal involvement and disease activity in SLE patients.
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spelling pubmed-47901842016-04-04 Correlation of plasma interleukin-18 concentration and severity of renal involvement and disease activity in systemic lupus erythematosus Jafari-Nakhjavani, Mohammad Reza Abedi-Azar, Sima Nejati, Babak J Nephropathol Original Article Background: Systemic lupus erythematosus (SLE) is a systemic autoimmune disease characterized by activation of T and polyclonal B lymphocytes. IL-18 was originally identified as a factor which enhances IFN-γ production and is a potent inducer of the inflammatory mediators by T cells, causing severe inflammatory disorders in SLE. Objectives: This study aimed to evaluate the association of plasma interlukine-18 (IL-18) concentration and severity of lupus nephritis (LN) and disease activity in SLE patients. Patients and Methods: In this cross-sectional study, 113 patients with SLE and 50 healthy individuals were examined. Serum level of IL-18 was measured. The severity and activity of the disease was determined by Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) score. The severity of kidney involvement was studied by renal biopsy, serum creatinine and 24 hours urine protein level. Results: The mean level of serum IL-18 was significantly higher in the patients than controls (577.67 ± 649.95 versus 60.48 ± 19.53 pg/ml; P < 0.001). In SLE patients with active disease level of serum IL-18 was significantly higher than chronic disease (622.77 ± 716.54 versus 182 ± 184.37 pg/ml; P < 0.001). The serum level of IL-18 was significantly higher in stage IV (P < 0.001) and V (P < 0.001) of patients with LN, than other stages. Conclusions: The current study showed that the serum IL-18 is significantly higher in the patients than controls and it significantly correlated with sever renal involvement and disease activity in SLE patients. Society of Diabetic Nephropathy Prevention 2016-01 2015-11-08 /pmc/articles/PMC4790184/ /pubmed/27047807 http://dx.doi.org/10.15171/jnp.2016.05 Text en © 2016 The Author(s) Published by Society of Diabetic Nephropathy Prevention. This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jafari-Nakhjavani, Mohammad Reza
Abedi-Azar, Sima
Nejati, Babak
Correlation of plasma interleukin-18 concentration and severity of renal involvement and disease activity in systemic lupus erythematosus
title Correlation of plasma interleukin-18 concentration and severity of renal involvement and disease activity in systemic lupus erythematosus
title_full Correlation of plasma interleukin-18 concentration and severity of renal involvement and disease activity in systemic lupus erythematosus
title_fullStr Correlation of plasma interleukin-18 concentration and severity of renal involvement and disease activity in systemic lupus erythematosus
title_full_unstemmed Correlation of plasma interleukin-18 concentration and severity of renal involvement and disease activity in systemic lupus erythematosus
title_short Correlation of plasma interleukin-18 concentration and severity of renal involvement and disease activity in systemic lupus erythematosus
title_sort correlation of plasma interleukin-18 concentration and severity of renal involvement and disease activity in systemic lupus erythematosus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4790184/
https://www.ncbi.nlm.nih.gov/pubmed/27047807
http://dx.doi.org/10.15171/jnp.2016.05
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