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Elevated serum levels of human epididymis protein 4 in adult patients with proliferative lupus nephritis

BACKGROUND: This study aimed to access whether serum human epididymis protein 4 (HE4) level could identify lupus nephritis (LN) pathological classes in adults and children. METHODS: The serum HE4 levels of 190 healthy subjects and 182 patients with systemic lupus erythematosus (SLE) (61 adult-onset...

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Autores principales: Li, Liubing, Xu, Huiya, Le, Yuting, Li, Runzhao, Shi, Qiong, Zhu, Hongji, Xu, Hongxu, Li, Laisheng, Liu, Min, Wang, Fen, Zhang, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243370/
https://www.ncbi.nlm.nih.gov/pubmed/37287983
http://dx.doi.org/10.3389/fimmu.2023.1179986
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author Li, Liubing
Xu, Huiya
Le, Yuting
Li, Runzhao
Shi, Qiong
Zhu, Hongji
Xu, Hongxu
Li, Laisheng
Liu, Min
Wang, Fen
Zhang, Hui
author_facet Li, Liubing
Xu, Huiya
Le, Yuting
Li, Runzhao
Shi, Qiong
Zhu, Hongji
Xu, Hongxu
Li, Laisheng
Liu, Min
Wang, Fen
Zhang, Hui
author_sort Li, Liubing
collection PubMed
description BACKGROUND: This study aimed to access whether serum human epididymis protein 4 (HE4) level could identify lupus nephritis (LN) pathological classes in adults and children. METHODS: The serum HE4 levels of 190 healthy subjects and 182 patients with systemic lupus erythematosus (SLE) (61 adult-onset LN [aLN], 39 childhood-onset LN [cLN], and 82 SLE without LN) were determined using Architect HE4 kits and an Abbott ARCHITECT i2000SR Immunoassay Analyzer. RESULTS: Serum HE4 level was significantly higher in the aLN patients (median, 85.5 pmol/L) than in the patients with cLN (44 pmol/L, P < 0.001) or SLE without LN (37 pmol/L, P < 0.001), or the healthy controls (30 pmol/L, P < 0.001). Multivariate analysis showed that serum HE4 level was independently associated with aLN. Stratified by LN class, serum HE4 level was significantly higher in the patients with proliferative LN (PLN) than in those with non-PLN, and this difference was found only in aLN (median, 98.3 versus 49.3 pmol/L, P = 0.021) but not in cLN. Stratified by activity (A) and chronicity (C) indices, the aLN patients with class IV (A/C) possessed significantly higher serum HE4 levels than those with class IV (A) (median, 195.5 versus 60.8 pmol/L, P = 0.006), and this difference was not seen in the class III aLN or cLN patients. CONCLUSION: Serum HE4 level is elevated in patients with class IV (A/C) aLN. The role of HE4 in the pathogenesis of chronic lesions of class IV aLN needs further investigation.
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spelling pubmed-102433702023-06-07 Elevated serum levels of human epididymis protein 4 in adult patients with proliferative lupus nephritis Li, Liubing Xu, Huiya Le, Yuting Li, Runzhao Shi, Qiong Zhu, Hongji Xu, Hongxu Li, Laisheng Liu, Min Wang, Fen Zhang, Hui Front Immunol Immunology BACKGROUND: This study aimed to access whether serum human epididymis protein 4 (HE4) level could identify lupus nephritis (LN) pathological classes in adults and children. METHODS: The serum HE4 levels of 190 healthy subjects and 182 patients with systemic lupus erythematosus (SLE) (61 adult-onset LN [aLN], 39 childhood-onset LN [cLN], and 82 SLE without LN) were determined using Architect HE4 kits and an Abbott ARCHITECT i2000SR Immunoassay Analyzer. RESULTS: Serum HE4 level was significantly higher in the aLN patients (median, 85.5 pmol/L) than in the patients with cLN (44 pmol/L, P < 0.001) or SLE without LN (37 pmol/L, P < 0.001), or the healthy controls (30 pmol/L, P < 0.001). Multivariate analysis showed that serum HE4 level was independently associated with aLN. Stratified by LN class, serum HE4 level was significantly higher in the patients with proliferative LN (PLN) than in those with non-PLN, and this difference was found only in aLN (median, 98.3 versus 49.3 pmol/L, P = 0.021) but not in cLN. Stratified by activity (A) and chronicity (C) indices, the aLN patients with class IV (A/C) possessed significantly higher serum HE4 levels than those with class IV (A) (median, 195.5 versus 60.8 pmol/L, P = 0.006), and this difference was not seen in the class III aLN or cLN patients. CONCLUSION: Serum HE4 level is elevated in patients with class IV (A/C) aLN. The role of HE4 in the pathogenesis of chronic lesions of class IV aLN needs further investigation. Frontiers Media S.A. 2023-05-23 /pmc/articles/PMC10243370/ /pubmed/37287983 http://dx.doi.org/10.3389/fimmu.2023.1179986 Text en Copyright © 2023 Li, Xu, Le, Li, Shi, Zhu, Xu, Li, Liu, Wang and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Li, Liubing
Xu, Huiya
Le, Yuting
Li, Runzhao
Shi, Qiong
Zhu, Hongji
Xu, Hongxu
Li, Laisheng
Liu, Min
Wang, Fen
Zhang, Hui
Elevated serum levels of human epididymis protein 4 in adult patients with proliferative lupus nephritis
title Elevated serum levels of human epididymis protein 4 in adult patients with proliferative lupus nephritis
title_full Elevated serum levels of human epididymis protein 4 in adult patients with proliferative lupus nephritis
title_fullStr Elevated serum levels of human epididymis protein 4 in adult patients with proliferative lupus nephritis
title_full_unstemmed Elevated serum levels of human epididymis protein 4 in adult patients with proliferative lupus nephritis
title_short Elevated serum levels of human epididymis protein 4 in adult patients with proliferative lupus nephritis
title_sort elevated serum levels of human epididymis protein 4 in adult patients with proliferative lupus nephritis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243370/
https://www.ncbi.nlm.nih.gov/pubmed/37287983
http://dx.doi.org/10.3389/fimmu.2023.1179986
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