Serum Calprotectin as a Novel Biomarker of Disease Severity and Activity in Systemic Sclerosis Patients

A monocentric cross-sectional study was performed to investigate the role of serum calprotectin as a biomarker for disease severity and activity in systemic sclerosis (SSc). Serum calprotectin was measured in 74 consecutive SSc patients admitted to a tertiary hospital in Rome, and in 50 healthy controls (HCs) who were healthcare workers, using Aptiva's particle-based multianalyte technology. In SSc patients, a statistically significant correlation was found between calprotectin and the modified Rodnan skin score (mRSS) (r = 0.402, <i>p</i> < 0.001), disease activity index (DAI) (r = 0.420, <i>p</i> < 0.001), disease severity scale (DSS) (r = 0.365, <i>p</i> < 0.01), forced vital capacity (FVC) (r = -0.459, <i>p</i> < 0.001), and diffusion lung capacity for carbon monoxide (DLco) (r = -0.445, <i>p</i> < 0.001). Calprotectin was higher in SSc patients with digital ulcers (DUs) than in SSc patients without DUs [2.98 mcg/mL (IQR 2.07;4.29) vs. 2.08 mcg/mL (IQR 1.71;2.45), <i>p</i> < 0.01] and in SSc patients with interstitial lung disease (ILD) compared to SSc patients without ILD [2.56 mcg/mL (IQR 1.94;3.03) vs. 1.96 mcg/mL (IQR 1.7;2.35), <i>p</i> < 0.01]. The multivariable stepwise logistic regression analysis showed calprotectin to be independently associated with DUs [OR 2.531 (CI 95%: 1.074;5.961), <i>p</i> < 0.05] and ILD [OR 3.687 (CI 95%: 1.336;10.170), <i>p</i> < 0.05] in SSc patients. Serum calprotectin is associated with DUs and ILD in SSc patients.

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Journal
International Journal of Molecular Sciences
Published
2025-05-01
DOI
https://doi.org/10.3390/ijms26094290
Citations
3
Primary Topic
Systemic Sclerosis and Related Diseases
Type
article
Field-Weighted Citation Impact
4.41

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article

Serum Calprotectin as a Novel Biomarker of Disease Severity and Activity in Systemic Sclerosis Patients

Edoardo Rosato, Umberto Basile, Chiara Pellicano, Giancarlo D’Ippolito et al.
3 citations
International Journal of Molecular Sciences
Systemic Sclerosis and Related Diseases
4.41
article

Serum Calprotectin as a Novel Biomarker of Disease Severity and Activity in Systemic Sclerosis Patients

Edoardo Rosato, Umberto Basile, Chiara Pellicano, Giancarlo D’Ippolito, Valeria Carnazzo, Antonietta Gigante, Francesco Laterza, Ilaria Vinante, Annalisa Villa
article en
3 citations

Abstract

A monocentric cross-sectional study was performed to investigate the role of serum calprotectin as a biomarker for disease severity and activity in systemic sclerosis (SSc). Serum calprotectin was measured in 74 consecutive SSc patients admitted to a tertiary hospital in Rome, and in 50 healthy controls (HCs) who were healthcare workers, using Aptiva's particle-based multianalyte technology. In SSc patients, a statistically significant correlation was found between calprotectin and the modified Rodnan skin score (mRSS) (r = 0.402, <i>p</i> < 0.001), disease activity index (DAI) (r = 0.420, <i>p</i> < 0.001), disease severity scale (DSS) (r = 0.365, <i>p</i> < 0.01), forced vital capacity (FVC) (r = -0.459, <i>p</i> < 0.001), and diffusion lung capacity for carbon monoxide (DLco) (r = -0.445, <i>p</i> < 0.001). Calprotectin was higher in SSc patients with digital ulcers (DUs) than in SSc patients without DUs [2.98 mcg/mL (IQR 2.07;4.29) vs. 2.08 mcg/mL (IQR 1.71;2.45), <i>p</i> < 0.01] and in SSc patients with interstitial lung disease (ILD) compared to SSc patients without ILD [2.56 mcg/mL (IQR 1.94;3.03) vs. 1.96 mcg/mL (IQR 1.7;2.35), <i>p</i> < 0.01]. The multivariable stepwise logistic regression analysis showed calprotectin to be independently associated with DUs [OR 2.531 (CI 95%: 1.074;5.961), <i>p</i> < 0.05] and ILD [OR 3.687 (CI 95%: 1.336;10.170), <i>p</i> < 0.05] in SSc patients. Serum calprotectin is associated with DUs and ILD in SSc patients.

International Journal of Molecular SciencesVol. 26(9)
Ospedale Santa Maria Goretti (IT), Sapienza University of Rome (IT)
Sapienza Università di Roma
Openalex Percentile: Top 6%
Systemic Sclerosis and Related Diseases
4.41
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