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NLRC5: potential novel non-invasive biomarker for predicting and reflecting the progression of IgA nephritis

BACKGROUND: The nucleotide oligomerization domain-like receptor subfamily C5 (NLRC5) is primarily expressed in the adaptive and innate immune systems. NLRC5 was recently discovered to regulate immunity and inflammatory responses. Abnormal immune and inflammatory responses are considered critical pat...

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Autores principales: Chen, Yusa, Li, Huihui, Xiao, Chenggen, Zeng, Xiangli, Xiao, Xiangcheng, Zhou, Qiaoling, Xiao, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245714/
https://www.ncbi.nlm.nih.gov/pubmed/30453994
http://dx.doi.org/10.1186/s12967-018-1694-1
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author Chen, Yusa
Li, Huihui
Xiao, Chenggen
Zeng, Xiangli
Xiao, Xiangcheng
Zhou, Qiaoling
Xiao, Ping
author_facet Chen, Yusa
Li, Huihui
Xiao, Chenggen
Zeng, Xiangli
Xiao, Xiangcheng
Zhou, Qiaoling
Xiao, Ping
author_sort Chen, Yusa
collection PubMed
description BACKGROUND: The nucleotide oligomerization domain-like receptor subfamily C5 (NLRC5) is primarily expressed in the adaptive and innate immune systems. NLRC5 was recently discovered to regulate immunity and inflammatory responses. Abnormal immune and inflammatory responses are considered critical pathogenesis in IgA nephritis (IgAN). However, the role of NLRC5 in IgAN is unknown. We previously showed that NLRC5 can be detected in patients with IgAN; herein, we further examined the pathophysiological significance of NLRC5 in the serum and renal deposits of patients with IgAN. This study is the first to find that NLRC5 is closely correlated with IgAN. METHODS: IgAN patients (n = 50) who were diagnosed by renal biopsy provided blood and renal biopsy tissue, and age-matched healthy control subjects (blood donators n = 22; tissue donators n = 5) were included. Renal biopsies were diagnosed, and blood biochemical parameters were tested. Serum creatinine, urea, proteinuria, haematuria, albumin, and immunoglobulin A levels were recorded. Serum NLRC5 concentrations were detected by enzyme-linked immunosorbent assay, and tissue NLRC5 expression in kidney tissue was detected by immunohistochemical analysis. ROC curve analysis was used to evaluate the diagnostic value of the serum NLRC5 concentration in IgAN. RESULTS: Serum NLRC5 concentration was significantly decreased in the IgAN group compared to that in the healthy control group (P < 0.0001), especially in S1 (Oxford classification) patients (P < 0.0001). Furthermore, serum NLRC5 concentration had a negative correlation with Lee’s grade (r = 0.3526, P = 0.0060) and proteinuria levels (r = 0.4571, P = 0.0004). Tissue NLRC5 expression was significantly increased in the IgAN group compared to that in the healthy control group (P < 0.0001); a more significant increase was identified in the S1 group (P < 0.05) and had a positive correlation with Lee’s grade (r = 0.497, P < 0.0001). We proposed a cut-off value of 1415 pg/ml for serum NLRC5 concentration, which was able to predict IgAN with 77.27% sensitivity and 87.5% specificity. CONCLUSIONS: Serum NLRC5 concentrations in IgAN are significantly decreased, and tissue NLRC5 expression is significantly increased in IgAN renal tissue, which is consistent with pathological severity. This finding suggests that NLRC5 could potentially be a diagnostic index and represents a prognostic factor in IgAN patients.
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spelling pubmed-62457142018-11-26 NLRC5: potential novel non-invasive biomarker for predicting and reflecting the progression of IgA nephritis Chen, Yusa Li, Huihui Xiao, Chenggen Zeng, Xiangli Xiao, Xiangcheng Zhou, Qiaoling Xiao, Ping J Transl Med Research BACKGROUND: The nucleotide oligomerization domain-like receptor subfamily C5 (NLRC5) is primarily expressed in the adaptive and innate immune systems. NLRC5 was recently discovered to regulate immunity and inflammatory responses. Abnormal immune and inflammatory responses are considered critical pathogenesis in IgA nephritis (IgAN). However, the role of NLRC5 in IgAN is unknown. We previously showed that NLRC5 can be detected in patients with IgAN; herein, we further examined the pathophysiological significance of NLRC5 in the serum and renal deposits of patients with IgAN. This study is the first to find that NLRC5 is closely correlated with IgAN. METHODS: IgAN patients (n = 50) who were diagnosed by renal biopsy provided blood and renal biopsy tissue, and age-matched healthy control subjects (blood donators n = 22; tissue donators n = 5) were included. Renal biopsies were diagnosed, and blood biochemical parameters were tested. Serum creatinine, urea, proteinuria, haematuria, albumin, and immunoglobulin A levels were recorded. Serum NLRC5 concentrations were detected by enzyme-linked immunosorbent assay, and tissue NLRC5 expression in kidney tissue was detected by immunohistochemical analysis. ROC curve analysis was used to evaluate the diagnostic value of the serum NLRC5 concentration in IgAN. RESULTS: Serum NLRC5 concentration was significantly decreased in the IgAN group compared to that in the healthy control group (P < 0.0001), especially in S1 (Oxford classification) patients (P < 0.0001). Furthermore, serum NLRC5 concentration had a negative correlation with Lee’s grade (r = 0.3526, P = 0.0060) and proteinuria levels (r = 0.4571, P = 0.0004). Tissue NLRC5 expression was significantly increased in the IgAN group compared to that in the healthy control group (P < 0.0001); a more significant increase was identified in the S1 group (P < 0.05) and had a positive correlation with Lee’s grade (r = 0.497, P < 0.0001). We proposed a cut-off value of 1415 pg/ml for serum NLRC5 concentration, which was able to predict IgAN with 77.27% sensitivity and 87.5% specificity. CONCLUSIONS: Serum NLRC5 concentrations in IgAN are significantly decreased, and tissue NLRC5 expression is significantly increased in IgAN renal tissue, which is consistent with pathological severity. This finding suggests that NLRC5 could potentially be a diagnostic index and represents a prognostic factor in IgAN patients. BioMed Central 2018-11-19 /pmc/articles/PMC6245714/ /pubmed/30453994 http://dx.doi.org/10.1186/s12967-018-1694-1 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Chen, Yusa
Li, Huihui
Xiao, Chenggen
Zeng, Xiangli
Xiao, Xiangcheng
Zhou, Qiaoling
Xiao, Ping
NLRC5: potential novel non-invasive biomarker for predicting and reflecting the progression of IgA nephritis
title NLRC5: potential novel non-invasive biomarker for predicting and reflecting the progression of IgA nephritis
title_full NLRC5: potential novel non-invasive biomarker for predicting and reflecting the progression of IgA nephritis
title_fullStr NLRC5: potential novel non-invasive biomarker for predicting and reflecting the progression of IgA nephritis
title_full_unstemmed NLRC5: potential novel non-invasive biomarker for predicting and reflecting the progression of IgA nephritis
title_short NLRC5: potential novel non-invasive biomarker for predicting and reflecting the progression of IgA nephritis
title_sort nlrc5: potential novel non-invasive biomarker for predicting and reflecting the progression of iga nephritis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245714/
https://www.ncbi.nlm.nih.gov/pubmed/30453994
http://dx.doi.org/10.1186/s12967-018-1694-1
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