Evaluation of serum fibroblast growth factor-23 in patients with axial spondyloarthritis and its association with sclerostin, inflammation, and spinal damage

• Published in: Rheumatology international Vol. 39; no. 5; pp. 835 - 840
• Main Authors: Gercik, Onay, Solmaz, Dilek, Coban, Eyup, Iptec, Betul Ozbek, Avcioglu, Gamze, Bayindir, Ozun, Kabadayi, Gokhan, Topal, Fatih Esad, Kozaci, Didem, Akar, Servet
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.05.2019; Springer Nature B.V
• Subjects: Adaptor Proteins, Signal Transducing - blood; Adult; Blood Sedimentation; Female; Fibroblast Growth Factors - blood; Fibroblasts; Growth factors; Humans; Inflammation; Male; Medicine; Medicine & Public Health; Middle Aged; Observational Research; Rheumatology; Severity of Illness Index; Spine - diagnostic imaging; Spondylarthropathies - blood; Spondylitis, Ankylosing - blood; Spondylitis, Ankylosing - diagnostic imaging; Sclerostin; Fibroblast growth factor-23; Spondyloarthritis; Ankylosing spondylitis
• ISSN: 0172-8172; 1437-160X; 1437-160X
• DOI: 10.1007/s00296-019-04298-5

The mechanisms underlying new bone formation in individuals with axial spondyloarthritis (axSpA) remain unclear; however, low levels of sclerostin (SOST) may be associated with development of syndesmophytes in those with ankylosing spondylitis (AS). Expression of fibroblast growth factor-23 (FGF-23), another osteocyte factor, is high in those with osteoporosis and chronic renal failure, but levels in those with axSpA are unknown. To evaluate serum FGF-23 and SOST levels in axSpA patients, and to assess their relationship with inflammation and structural damage. In total, 109 axSpA patients (55 with AS and 54 with non-radiographic axSpA) and 57 healthy control (HC) subjects were included in the analysis. Serum concentrations of FGF-23 and SOST were measured and correlation analysis was performed. The presence of syndesmophytes and the modified Stoke Ankylosing Spondylitis Spinal Score (mSASSS) were used to assess structural damage. Levels of serum FGF-23 in axSpA patients were significantly higher than those in HCs [median (interquartile range—IQR) FGF-23 level, pg/ml; AxSpA = 144 (82.3–253.2), HC = 107 (63.3–192.8), p  = 0.010]; however, there was no difference in SOST levels. FGF-23 levels correlated with the erythrocyte sedimentation rate (ESR) ( r  = 0.265, p  = 0.006) and serum C-reactive protein (CRP) level ( r  = 0.229, p  = 0.010). In the axSpA, SOST levels correlated negatively with mSASSS ( r  = − 0.283, p  = 0.007), whereas those in the AS group correlated negatively with CRP ( r  = − 0.426, p  = 0.001). Serum FGF-23 levels were high in axSpA patients. Increased FGF-23 was associated with inflammation, but not with SOST levels or disease activity. SOST correlated negatively with both inflammation and structural damage.