Serum complement 3 is a potential biomarker for assessing disease activity in Takayasu arteritis
Open Access
- 24 February 2021
- journal article
- research article
- Published by Springer Nature in Arthritis Research & Therapy
- Vol. 23 (1) , 1-8
Abstract
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.Keywords
All Related Versions
Funding Information
- National Natural Science Foundation of China (81771730, 81801598)
This publication has 22 references indexed in Scilit:
- A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohortBMC Neurology, 2014
- Complement in ANCA-Associated VasculitisSeminars in Nephrology, 2013
- Pathology of Takayasu arteritis: A brief reviewAnnals of Pediatric Cardiology, 2013
- Circulating complement activation in patients with anti-neutrophil cytoplasmic antibody–associated vasculitisKidney International, 2013
- Pathogenesis of Takayasu's arteritis: A 2011 updateAutoimmunity Reviews, 2011
- Assessment of disease activity and progression in Takayasu’s arteritis with Disease Extent Index-TakayasuRheumatology, 2010
- Circulation levels of acute phase proteins in patients with Takayasu arteritisJournal of Vascular Surgery, 2010
- Takayasu arteritis: a reviewJournal of Clinical Pathology, 2002
- Takayasu ArteritisAnnals of Internal Medicine, 1994
- The American College of Rheumatology 1990 criteria for the classification of takayasu arteritisArthritis & Rheumatism, 1990