| Literature DB >> 31025138 |
Hana Hulejová1, Tereza Kropáčková2,3, Kristýna Bubová2,3, Olga Kryštůfková2,3, Mária Filková2,3, Heřman Mann2,3, Šárka Forejtová2,3, Michal Tomčík2,3, Jiří Vencovský2,3, Karel Pavelka2,3, Ladislav Šenolt2,3.
Abstract
The purpose of this cross-sectional study was to assess the visfatin levels in patients with axial spondyloarthritis (axSpA) and to investigate the association between visfatin, disease activity and radiographic spinal damage. Serum visfatin levels were determined by enzyme-linked immunosorbent assay in 64 patients with axSpA (46 with radiographic axSpA (r-axSpA) and 18 with non-radiographic axSpA (nr-axSpA)) and 61 age-/sex-matched healthy individuals. Patients with r-axSpA were further divided into two subsets based on radiographic spinal damage using modified Stoke Ankylosing Spondylitis Spine Score (mSASSS = 0 and mSASSS ≥ 1). The Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) was used to assess disease activity. C-reactive protein (CRP) levels and human leukocyte antigen (HLA)-B27 were determined. Visfatin levels were significantly higher in patients with axSpA and in the subgroup of patients with r-axSpA than in healthy individuals (p = 0.010 and p = 0.005, respectively), with no difference between patients with r-axSpA and with nr-axSpA. In general, disease activity was high (mean BASDAI 5.01) and was moderately correlated with visfatin levels (r = 0.585; p = 0.011) in patients with nr-axSpA. Visfatin levels correlated with mSASSS (r = 0.281; p = 0.026) and were significantly higher in axSpA patients with mSASSS ≥ 1 than in those with mSASSS = 0 (p = 0.025). Our study showed that circulating visfatin levels are elevated in axSpA patients, may be associated with disease activity in early phase of the disease and with the degree of radiographic spinal involvement.Entities:
Keywords: Axial spondyloarthritis; Disease activity; Radiographic damage; Visfatin
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Year: 2019 PMID: 31025138 DOI: 10.1007/s00296-019-04301-z
Source DB: PubMed Journal: Rheumatol Int ISSN: 0172-8172 Impact factor: 2.631