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Plasma soluble tumor necrosis factor receptor I as a biomarker of lupus nephritis and disease activity in systemic lupus erythematosus patients

The goal of our study was to evaluate the potential role of sTNF-RI as a biomarker of renal involvement in SLE patients and active SLE. The study sample consisted of two cohorts. The discovery cohort included 16 SLE patients without renal involvement (non-LN), 60 lupus nephritis (LN) patients and 21...

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Published in:Renal failure 2023-12, Vol.45 (1), p.2174355-2174355
Main Authors: Liu, Xin-ran, Qi, Yuan-yuan, Zhao, Ya-fei, Cui, Yan, Zhao, Zhan-zheng
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description The goal of our study was to evaluate the potential role of sTNF-RI as a biomarker of renal involvement in SLE patients and active SLE. The study sample consisted of two cohorts. The discovery cohort included 16 SLE patients without renal involvement (non-LN), 60 lupus nephritis (LN) patients and 21 healthy controls (HCs) and the replication cohort included 18 SLE non-LN patients, 116 LN patients and 36 HCs. The sTNF-RI levels differed significantly in the discovery cohort. The plasma sTNF-RI levels were higher in LN patients than in non-LN patients (p = .009) and HCs (p = 4 × 10 −6 ). Plasma sTNF-RI levels were significantly higher in non-LN patients than in HCs (p = .03). The finding was confirmed in independent replication cohort (LNs vs. non-LN, p = 4.053 × 10 −7 ; LNs vs. HCs, p = 2.395 × 10 −18 ; non-LN vs. HCs, p = 2.51 × 10 −4 ). The plasma sTNF-RI levels were associated with disease activity, renal function in SLE patients and urine protein in LN patients. The multivariate analysis revealed that high sTNF-RI was an independent risk factor for renal involvement. The multivariate logistic regression results suggested that high TNF-RI, high systolic blood pressure, high serum creatinine, low C4 and positive anti-dsDNA were independent risks of active SLE patients. A nomogram was constructed based on the results of multivariate logistic regression analysis and it was practical in predicting the risk of the active SLE patients. Immunohistochemistry suggested that the expression of TNF-RI in the kidney was increased. Plasma sTNF-RI might be a good biomarker of renal involvement and disease activity in SLE patients.
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The study sample consisted of two cohorts. The discovery cohort included 16 SLE patients without renal involvement (non-LN), 60 lupus nephritis (LN) patients and 21 healthy controls (HCs) and the replication cohort included 18 SLE non-LN patients, 116 LN patients and 36 HCs. The sTNF-RI levels differed significantly in the discovery cohort. The plasma sTNF-RI levels were higher in LN patients than in non-LN patients (p = .009) and HCs (p = 4 × 10 −6 ). Plasma sTNF-RI levels were significantly higher in non-LN patients than in HCs (p = .03). The finding was confirmed in independent replication cohort (LNs vs. non-LN, p = 4.053 × 10 −7 ; LNs vs. HCs, p = 2.395 × 10 −18 ; non-LN vs. HCs, p = 2.51 × 10 −4 ). The plasma sTNF-RI levels were associated with disease activity, renal function in SLE patients and urine protein in LN patients. The multivariate analysis revealed that high sTNF-RI was an independent risk factor for renal involvement. The multivariate logistic regression results suggested that high TNF-RI, high systolic blood pressure, high serum creatinine, low C4 and positive anti-dsDNA were independent risks of active SLE patients. A nomogram was constructed based on the results of multivariate logistic regression analysis and it was practical in predicting the risk of the active SLE patients. Immunohistochemistry suggested that the expression of TNF-RI in the kidney was increased. Plasma sTNF-RI might be a good biomarker of renal involvement and disease activity in SLE patients.</description><identifier>ISSN: 0886-022X</identifier><identifier>EISSN: 1525-6049</identifier><identifier>DOI: 10.1080/0886022X.2023.2174355</identifier><identifier>PMID: 36946374</identifier><language>eng</language><publisher>England: Taylor &amp; Francis</publisher><subject>Anti-DNA antibodies ; Biomarkers ; Blood pressure ; Clinical Study ; Creatinine ; disease activity ; Humans ; Immunohistochemistry ; Kidney ; Lupus ; Lupus Erythematosus, Systemic - complications ; Lupus nephritis ; Lupus Nephritis - complications ; Multivariate analysis ; Plasma ; Receptors, Tumor Necrosis Factor ; Regression analysis ; Renal function ; Replication ; Risk factors ; Systemic lupus erythematosus ; Tumor necrosis factor ; tumor necrosis factor receptor ; Tumor necrosis factor-TNF</subject><ispartof>Renal failure, 2023-12, Vol.45 (1), p.2174355-2174355</ispartof><rights>2023 The Author(s). 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The multivariate logistic regression results suggested that high TNF-RI, high systolic blood pressure, high serum creatinine, low C4 and positive anti-dsDNA were independent risks of active SLE patients. A nomogram was constructed based on the results of multivariate logistic regression analysis and it was practical in predicting the risk of the active SLE patients. Immunohistochemistry suggested that the expression of TNF-RI in the kidney was increased. Plasma sTNF-RI might be a good biomarker of renal involvement and disease activity in SLE patients.</abstract><cop>England</cop><pub>Taylor &amp; Francis</pub><pmid>36946374</pmid><doi>10.1080/0886022X.2023.2174355</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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source Taylor & Francis Open Access; Publicly Available Content Database; PubMed
subjects Anti-DNA antibodies
Biomarkers
Blood pressure
Clinical Study
Creatinine
disease activity
Humans
Immunohistochemistry
Kidney
Lupus
Lupus Erythematosus, Systemic - complications
Lupus nephritis
Lupus Nephritis - complications
Multivariate analysis
Plasma
Receptors, Tumor Necrosis Factor
Regression analysis
Renal function
Replication
Risk factors
Systemic lupus erythematosus
Tumor necrosis factor
tumor necrosis factor receptor
Tumor necrosis factor-TNF
title Plasma soluble tumor necrosis factor receptor I as a biomarker of lupus nephritis and disease activity in systemic lupus erythematosus patients
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