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Diagnostic performance of serum cystatin C and complement component 1q in lupus nephritis
BACKGROUND: The information concerning non-invasive, easily obtainable, and accurate biomarkers for diagnosis of lupus nephritis (LN) is extremely limited. The aim of this study was to evaluate the diagnostic performance of cystatin C (CysC) and complement component 1q (C1q) for LN. METHODS: A case-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894121/ https://www.ncbi.nlm.nih.gov/pubmed/31801580 http://dx.doi.org/10.1186/s13075-019-2065-x |
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author | Xu, Bei Zhang, Ya-mei Yang, Yu-wei Liu, Yun-shuang Feng, Jia-fu |
author_facet | Xu, Bei Zhang, Ya-mei Yang, Yu-wei Liu, Yun-shuang Feng, Jia-fu |
author_sort | Xu, Bei |
collection | PubMed |
description | BACKGROUND: The information concerning non-invasive, easily obtainable, and accurate biomarkers for diagnosis of lupus nephritis (LN) is extremely limited. The aim of this study was to evaluate the diagnostic performance of cystatin C (CysC) and complement component 1q (C1q) for LN. METHODS: A case-control study that included 905 patients with systemic lupus erythematosus (SLE) without LN (group SLE), 334 patients with active lupus nephritis (group LNA), 255 patients with inactive lupus nephritis (group LNI), and 497 healthy individuals (group HC) was performed in Mianyang Central Hospital from March 2017 to December 2018. The serum levels of CysC, C1q, urea (Urea), and creatinine (Creat) were measured, and 2 estimated glomerular filtration rates (eGFR(CysC) and eGFR(Creat)) were calculated by equations which were based on serum CysC established by our group and the modification of diet in renal disease (MDRD), respectively. ANOVA analysis or Kruskal-Wallis test was used for comparing the differences among the groups, and receiver operating characteristic (ROC) curve was applied to identify the diagnostic efficiencies of individual or combined multiple indicators. RESULTS: Significantly elevated CysC and decreased C1q were observed in the LNA and LNI groups, which was in contrast to their levels in the SLE and HC groups. CysC (AUC = 0.906) or eGFR(CysC) (AUC = 0.907) assessed the highest diagnostic performance on LNA when detected individually, followed by C1q (AUC = 0.753). Joint utilization of C1q and CysC achieved very good performance (AUC = 0.933) which approximated to the best one observed in the combinations of C1q, Urea, CysC, eGFR(Creat), and Creat (AUC = 0.975). CONCLUSION: The separately detected CysC (eGFR(CysC)) and C1q were superior to the conventional biomarkers Urea, Creat, and eGFR(Creat) in the diagnosis of LNA. Moreover, although the combined detection of Urea, Creat, C1q, CysC, and eGFR(Creat) had the greatest diagnostic performance, the joint utilization of CysC and C1q could be prioritized for rapid discrimination of LNA if the economic burden is taken into consideration. |
format | Online Article Text |
id | pubmed-6894121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68941212019-12-11 Diagnostic performance of serum cystatin C and complement component 1q in lupus nephritis Xu, Bei Zhang, Ya-mei Yang, Yu-wei Liu, Yun-shuang Feng, Jia-fu Arthritis Res Ther Research Article BACKGROUND: The information concerning non-invasive, easily obtainable, and accurate biomarkers for diagnosis of lupus nephritis (LN) is extremely limited. The aim of this study was to evaluate the diagnostic performance of cystatin C (CysC) and complement component 1q (C1q) for LN. METHODS: A case-control study that included 905 patients with systemic lupus erythematosus (SLE) without LN (group SLE), 334 patients with active lupus nephritis (group LNA), 255 patients with inactive lupus nephritis (group LNI), and 497 healthy individuals (group HC) was performed in Mianyang Central Hospital from March 2017 to December 2018. The serum levels of CysC, C1q, urea (Urea), and creatinine (Creat) were measured, and 2 estimated glomerular filtration rates (eGFR(CysC) and eGFR(Creat)) were calculated by equations which were based on serum CysC established by our group and the modification of diet in renal disease (MDRD), respectively. ANOVA analysis or Kruskal-Wallis test was used for comparing the differences among the groups, and receiver operating characteristic (ROC) curve was applied to identify the diagnostic efficiencies of individual or combined multiple indicators. RESULTS: Significantly elevated CysC and decreased C1q were observed in the LNA and LNI groups, which was in contrast to their levels in the SLE and HC groups. CysC (AUC = 0.906) or eGFR(CysC) (AUC = 0.907) assessed the highest diagnostic performance on LNA when detected individually, followed by C1q (AUC = 0.753). Joint utilization of C1q and CysC achieved very good performance (AUC = 0.933) which approximated to the best one observed in the combinations of C1q, Urea, CysC, eGFR(Creat), and Creat (AUC = 0.975). CONCLUSION: The separately detected CysC (eGFR(CysC)) and C1q were superior to the conventional biomarkers Urea, Creat, and eGFR(Creat) in the diagnosis of LNA. Moreover, although the combined detection of Urea, Creat, C1q, CysC, and eGFR(Creat) had the greatest diagnostic performance, the joint utilization of CysC and C1q could be prioritized for rapid discrimination of LNA if the economic burden is taken into consideration. BioMed Central 2019-12-04 2019 /pmc/articles/PMC6894121/ /pubmed/31801580 http://dx.doi.org/10.1186/s13075-019-2065-x Text en © The Author(s). 2019 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 Article Xu, Bei Zhang, Ya-mei Yang, Yu-wei Liu, Yun-shuang Feng, Jia-fu Diagnostic performance of serum cystatin C and complement component 1q in lupus nephritis |
title | Diagnostic performance of serum cystatin C and complement component 1q in lupus nephritis |
title_full | Diagnostic performance of serum cystatin C and complement component 1q in lupus nephritis |
title_fullStr | Diagnostic performance of serum cystatin C and complement component 1q in lupus nephritis |
title_full_unstemmed | Diagnostic performance of serum cystatin C and complement component 1q in lupus nephritis |
title_short | Diagnostic performance of serum cystatin C and complement component 1q in lupus nephritis |
title_sort | diagnostic performance of serum cystatin c and complement component 1q in lupus nephritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894121/ https://www.ncbi.nlm.nih.gov/pubmed/31801580 http://dx.doi.org/10.1186/s13075-019-2065-x |
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