Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2025 May;44(5):2009-2021.
doi: 10.1007/s10067-025-07412-0. Epub 2025 Apr 2.

Serum ferritin is a superior biomarker for evaluating disease activity and kidney injury compared with C-reactive protein in anti-neutrophil cytoplasmic antibody-associated vasculitis

Affiliations
Comparative Study

Serum ferritin is a superior biomarker for evaluating disease activity and kidney injury compared with C-reactive protein in anti-neutrophil cytoplasmic antibody-associated vasculitis

Li-Yuan Xie et al. Clin Rheumatol. 2025 May.

Abstract

Background: Elevated C-reactive protein (CRP) is a characteristic of active anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). However, its relationship with organ involvement severity is ambiguous. Serum ferritin (SF) is a proinflammatory marker elevated in many autoimmune diseases, yet its role in AAV is poorly studied.

Methods: A total of 399 AAV patients were retrospectively selected and divided into four groups based on SF and CRP levels. Clinical, laboratory, and pathological data were compared. Survival analyses were conducted to estimate end-stage renal disease (ESRD) and death.

Results: In this cohort, 256 patients (64.16%) had elevated SF, and 289 (72.43%) had elevated CRP. Patients with elevated SF and normal CRP had the highest BVAS, lowest initial estimated glomerular filtration rate, highest 24-h proteinuria, and worst renal prognosis. SF showed a weak positive correlation with BVAS (R = 0.201, p < 0.001), while CRP showed a weak negative correlation with proteinuria (R = - 0.158, p = 0.002). Univariate Cox regression analysis revealed high SF level was a risk factor for ESRD and death, whereas CRP was not. Pathological tests showed that patients with elevated SF had a higher proportion of glomeruli with cellular crescents compared to those with normal SF. CRP positively correlated serum complement 3 (C3) with SF as a control variable (R = 0.434, p < 0.001), while SF negatively correlated with C3 with CRP as a control variable (R = - 0.201, p < 0.001).

Conclusion: In active AAV, high SF is associated with severe injury and poor kidney prognosis, whereas CRP is not. The underlying mechanism may be related to the different impacts on the complement system. Key Points • Patients with elevated SF and normal CRP had the highest BVAS, lowest initial estimated glomerular filtration rate, highest 24-hour proteinuria, and worst renal prognosis. . • CRP positively correlated serum C3 with SF as a control variable, while SF negatively correlated with C3 with CRP as a control variable. • High SF reflects a high proportion of glomeruli with cellular crescents in renal histopathology.

Keywords: Anti-neutrophil cytoplasmic antibody-associated vasculitis; Biomarker; C-reactive protein; Serum ferritin.

PubMed Disclaimer

Conflict of interest statement

Declarations. Ethics approval: The study was conducted by the ethical principles of the Helsinki Declaration and was approved by the Research Ethics Committee of Tianjin Medical University General Hospital (approval number: IRB2024-YX-572–01). The ethical committee waived the need for informed consent. Conflict of interest: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

    1. Kronbichler A, Lee KH, Denicolò S, Choi D, Lee H, Ahn D, Kim KH, Lee JH, Kim H, Hwang M et al (2020) Immunopathogenesis of ANCA-associated vasculitis. Int J Mol Sci 21(19):7319
    1. Kitching AR, Anders HJ, Basu N, Brouwer E, Gordon J, Jayne DR, Kullman J, Lyons PA, Merkel PA, Savage COS et al (2020) ANCA-associated vasculitis. Nature Rev Dis Prim 6(1):71 - DOI
    1. Kronbichler A, Bajema IM, Bruchfeld A, Mastroianni Kirsztajn G, Stone JH (2024) Diagnosis and management of ANCA-associated vasculitis. Lancet (London, England) 403(10427):683–698 - DOI - PubMed
    1. Solans-Laqué R, Fraile G, Rodriguez-Carballeira M, Caminal L, Castillo MJ, Martínez-Valle F, Sáez L, Rios JJ, Solanich X, Oristrell J et al (2017) Clinical characteristics and outcome of Spanish patients with ANCA-associated vasculitides: impact of the vasculitis type, ANCA specificity, and treatment on mortality and morbidity. Medicine 96(8):e6083 - DOI - PubMed - PMC
    1. Tian Y, Liu N, Yin H, Duan L (2022) Relationship between C-reactive protein/serum albumin ratio, neutrophil/lymphocyte ratio, and ANCA-associated vasculitis activity: a retrospective single center cohort study. Front Med 9:855869 - DOI

Publication types

LinkOut - more resources