Serum Levels of S100A8/A9 as a Biomarker of Disease Activity in Patients with IgA Vasculitis

Author:

Srsen Sasa12ORCID,Held Martina34ORCID,Sestan Mario34ORCID,Kifer Nastasia34,Kozmar Ana45ORCID,Supe Domic Daniela67,Benzon Benjamin2ORCID,Gagro Alenka489,Frkovic Marijan34ORCID,Jelusic Marija34ORCID

Affiliation:

1. Department of Paediatrics, University Hospital Split, Spinciceva 1, 21000 Split, Croatia

2. School of Medicine, University of Split, Soltanska 2, 21000 Split, Croatia

3. Department of Paediatrics, University Hospital Centre Zagreb, Kispaticeva 12, 10000 Zagreb, Croatia

4. School of Medicine, University of Zagreb, Salata 3, 10000 Zagreb, Croatia

5. Department of Laboratory Diagnostics, University Hospital Centre Zagreb, Kispaticeva 12, 10000 Zagreb, Croatia

6. Department of Medical Laboratory Diagnostic, University Hospital Split, Spinciceva 1, 21000 Split, Croatia

7. Department of Health Studies, University of Split, Ulica Rudjera Boskovica 35, 21000 Split, Croatia

8. Department of Paediatrics, Children’s Hospital Zagreb, Ulica Vjekoslava Klaica 16, 10000 Zagreb, Croatia

9. Medical Faculty Osijek, Josip Juraj Strossmayer University of Osijek, Josipa Huttlera 4, 31000 Osijek, Croatia

Abstract

S100A8/A9 protein is a well-known marker of disease activity or severity in many autoimmune and autoinflammatory diseases, but there have not been many studies about the role of S100A8/A9 in IgA vasculitis (IgAV). The aim of our study was to evaluate S100A8/A9 as a possible biomarker of activity in IgAV. We measured the serum levels of S100A8/A9 in pediatric patients with IgA vasculitis at the onset of the disease, after three months, and after six months. We compared these levels between patients with active disease, remission, and a control group, and assessed their correlation with disease activity and other markers of inflammation. Patients with active disease had significantly higher levels of serum S100A8/A9 (median ± SD) than those in the control group at the beginning of the disease (5740 ± 3157 ng/mL vs. 1447 ± 858.3 ng/mL; p < 0.0001), but also three months and six months after disease onset (p < 0.001). There was a positive correlation between S100A8/A9 serum levels and disease activity (p = 0.0003). Patients with active disease had significantly higher levels of S100A8/A9 than those in remission three months after disease onset (p = 0.0260). There was a correlation between S100A8/A9 and C-reactive protein, the C3 component of complement, ferritin, and fibrinogen. Serum levels of S100A8/A9 were also higher in patients with greater skin areas covered with rash. We demonstrated that serum levels of S100A8/A9 correlated well with disease activity and other biomarkers of inflammation in children with IgAV. According to our results, serum S100A8/A9 may be a good indicator of active disease in IgAV.

Funder

Croatian Science Foundation

Publisher

MDPI AG

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