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Serum complement 3 is a potential biomarker for assessing disease activity in Takayasu arteritis

BACKGROUND: Takayasu arteritis (TA) is a rare disease, lacking convenient and feasible biomarkers to identify disease activity. We aimed to evaluate the value of complements in distinguishing active TA. METHODS: Consecutive patients were enrolled from the prospective East China TA cohort from April...

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Autores principales: Chen, Rongyi, Ma, Lingying, Lv, Peng, Lin, Jiang, Li, Chaolun, Yan, Yan, Jin, Xuejuan, Dai, Xiaomin, Ji, Zongfei, Chen, Huiyong, Ma, Lili, Sun, Ying, Jiang, Lindi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903686/
https://www.ncbi.nlm.nih.gov/pubmed/33627173
http://dx.doi.org/10.1186/s13075-021-02433-x
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author Chen, Rongyi
Ma, Lingying
Lv, Peng
Lin, Jiang
Li, Chaolun
Yan, Yan
Jin, Xuejuan
Dai, Xiaomin
Ji, Zongfei
Chen, Huiyong
Ma, Lili
Sun, Ying
Jiang, Lindi
author_facet Chen, Rongyi
Ma, Lingying
Lv, Peng
Lin, Jiang
Li, Chaolun
Yan, Yan
Jin, Xuejuan
Dai, Xiaomin
Ji, Zongfei
Chen, Huiyong
Ma, Lili
Sun, Ying
Jiang, Lindi
author_sort Chen, Rongyi
collection PubMed
description BACKGROUND: Takayasu arteritis (TA) is a rare disease, lacking convenient and feasible biomarkers to identify disease activity. We aimed to evaluate the value of complements in distinguishing active TA. METHODS: Consecutive patients were enrolled from the prospective East China TA cohort from April 2008 to June 2019. Patients were divided into two groups according to their baseline Kerr score. The value of complements and other biomarkers in identifying disease activity were analysed with cluster analysis, ROC curves, and combined tests. An independent group of patients from July 2019 to December 2019 were employed to validate the results. RESULTS: Of the enrolled 519 patients, 406 (72.2%) cases were identified as active disease. Higher erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), interleukin-6 (IL-6), and complement 3 (C3) levels were observed in the active group. Elevated C3 (≥ 1.085 g/L) had a high value to identify active TA with a sensitivity of 69.9%, specificity of 66.7%, and AUC of 0.715. Combining the CRP (≥ 10.65 g/L; sensitivity, 50.7%; specificity, 82.4%) and C3, the sensitivity could be improved to 85.1% in parallel test and the specificity could be improved to 94.1% in serial test. Validation was further performed to confirm the value of C3 for disease activity assessment. The accuracy of the parallel test of CRP and C3 in external validation with independent 53 TA cases was 72.73% with the AUC of 0.721. CONCLUSION: Elevated C3 could effectively evaluate the disease activity of TA, and C3 combining with CRP could further improve the disease activity evaluation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-021-02433-x.
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spelling pubmed-79036862021-03-01 Serum complement 3 is a potential biomarker for assessing disease activity in Takayasu arteritis Chen, Rongyi Ma, Lingying Lv, Peng Lin, Jiang Li, Chaolun Yan, Yan Jin, Xuejuan Dai, Xiaomin Ji, Zongfei Chen, Huiyong Ma, Lili Sun, Ying Jiang, Lindi Arthritis Res Ther Research Article BACKGROUND: Takayasu arteritis (TA) is a rare disease, lacking convenient and feasible biomarkers to identify disease activity. We aimed to evaluate the value of complements in distinguishing active TA. METHODS: Consecutive patients were enrolled from the prospective East China TA cohort from April 2008 to June 2019. Patients were divided into two groups according to their baseline Kerr score. The value of complements and other biomarkers in identifying disease activity were analysed with cluster analysis, ROC curves, and combined tests. An independent group of patients from July 2019 to December 2019 were employed to validate the results. RESULTS: Of the enrolled 519 patients, 406 (72.2%) cases were identified as active disease. Higher erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), interleukin-6 (IL-6), and complement 3 (C3) levels were observed in the active group. Elevated C3 (≥ 1.085 g/L) had a high value to identify active TA with a sensitivity of 69.9%, specificity of 66.7%, and AUC of 0.715. Combining the CRP (≥ 10.65 g/L; sensitivity, 50.7%; specificity, 82.4%) and C3, the sensitivity could be improved to 85.1% in parallel test and the specificity could be improved to 94.1% in serial test. Validation was further performed to confirm the value of C3 for disease activity assessment. The accuracy of the parallel test of CRP and C3 in external validation with independent 53 TA cases was 72.73% with the AUC of 0.721. CONCLUSION: Elevated C3 could effectively evaluate the disease activity of TA, and C3 combining with CRP could further improve the disease activity evaluation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-021-02433-x. BioMed Central 2021-02-24 2021 /pmc/articles/PMC7903686/ /pubmed/33627173 http://dx.doi.org/10.1186/s13075-021-02433-x Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Chen, Rongyi
Ma, Lingying
Lv, Peng
Lin, Jiang
Li, Chaolun
Yan, Yan
Jin, Xuejuan
Dai, Xiaomin
Ji, Zongfei
Chen, Huiyong
Ma, Lili
Sun, Ying
Jiang, Lindi
Serum complement 3 is a potential biomarker for assessing disease activity in Takayasu arteritis
title Serum complement 3 is a potential biomarker for assessing disease activity in Takayasu arteritis
title_full Serum complement 3 is a potential biomarker for assessing disease activity in Takayasu arteritis
title_fullStr Serum complement 3 is a potential biomarker for assessing disease activity in Takayasu arteritis
title_full_unstemmed Serum complement 3 is a potential biomarker for assessing disease activity in Takayasu arteritis
title_short Serum complement 3 is a potential biomarker for assessing disease activity in Takayasu arteritis
title_sort serum complement 3 is a potential biomarker for assessing disease activity in takayasu arteritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903686/
https://www.ncbi.nlm.nih.gov/pubmed/33627173
http://dx.doi.org/10.1186/s13075-021-02433-x
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