Plasma heat shock protein 90 levels in patients with spondyloarthritis and their relation to structural changes: a cross-sectional study

Author:

Bubova Kristyna12ORCID,Storkanova Hana12,Oreska Sabina12,Spiritovic Maja13,Hermankova Barbora3,Mintalova Katerina1,Gregova Monika12,Husakova Marketa12,Horinkova Jana12,Forejtova Sarka12,Gatterova Jindriska12,Stolfa Jiri12,Komarc Martin4,Vencovsky Jiri12,Pavelka Karel12,Senolt Ladislav12,Tomcik Michal12ORCID

Affiliation:

1. Institute of Rheumatology, Prague, Czech Republic

2. Department of Rheumatology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic

3. Department of Physiotherapy, Faculty of Physical Education & Sport, Charles University, Prague, Czech Republic

4. Department of Methodology, Faculty of Physical Education & Sport, Charles University, Prague, Czech Republic

Abstract

Aim: Heat shock protein 90 (Hsp90) is a molecular chaperone regulating immune response. We aimed to assess systemic Hsp90 as a biomarker for spondyloarthritis (SpA). Materials & methods: Total of 80 axial SpA (axSpA) and 22 psoriatic arthritis patients and a corresponding number of age- and sex-matched healthy controls (HC) were included. Plasma Hsp90 levels were measured by ELISA. Results: Hsp90 was significantly increased in axSpA patients compared with HC (median interquartile range: 15.7 [10.5–19.8] vs 8.3 [6.6–11.8] ng/ml, p < 0.001). Moreover, Hsp90 was superior to C-reactive protein in differentiating axSpA (and both radiographic axSpA [r-axSpA] and nonradiographic-axSpA) from HC. Hsp90 levels correlated with bone marrow edema of sacroiliac joints in r-axSpA patients (r = 0.594, p = 0.019). Conclusion: Hsp90 could become a biomarker for active inflammation in r-axSpA, and can better distinguish axSpA patients from healthy subjects than C-reactive protein.

Funder

Ministry of Health of the Czech Republic

Charles University in Prague

Publisher

Future Medicine Ltd

Subject

Biochemistry (medical),Clinical Biochemistry,Drug Discovery

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