Serum levels of angiogenic cytokines in psoriatic arthritis and SAPHO syndrome

被引:27
作者
Przepiera-Bedzak, Hanna [1 ]
Fischer, Katarzyna [2 ]
Brzosko, Marek [1 ]
机构
[1] Pomorski Uniwersytet Med, Klin Reumatol & Chorob Wewnetrznych, PL-71252 Szczecin, Poland
[2] Pomorski Uniwersytet Med, Independent Lab Rheumat Diagnost, PL-71252 Szczecin, Poland
来源
POLSKIE ARCHIWUM MEDYCYNY WEWNETRZNEJ-POLISH ARCHIVES OF INTERNAL MEDICINE | 2013年 / 123卷 / 06期
关键词
epidermal growth factor; fibroblast growth factor; psoriatic arthritis; SAPHO syndrome; vascular endothelial growth factor; ENDOTHELIAL GROWTH-FACTOR; ANKYLOSING-SPONDYLITIS; DISEASE-ACTIVITY; RHEUMATOID-ARTHRITIS; BATH; VESSELS; VEGF;
D O I
10.20452/pamw.1772
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
INTRODUCTION Angiogenesis is involved in the pathogenesis of arthritis. OBJECTIVES The aim of the study was to assess the serum levels of selected angiogenic cytokines and their association with clinical presentation in patients with psoriatic arthritis (PsA) and SAPHO syndrome. PATIENTS AND METHODS We studied 98 patients: 80 with PsA and 18 with SAPHO syndrome. The following data were recorded: age, sex, disease duration, joint involvement, type of psoriasis, nail involvement, and treatment. The following indices used to assess the activity of PsA and SAPHO were measured: PASI, BASDAI, BASFI, BASMI, BASG, and VAS pain. We determined erythrocyte sedimentation rate, C-reactive protein (CRP), and platelet count. The serum levels of vascular endothelial growth factor (VEGF), epidermal growth factor (EGF), basic and acidic fibroblast growth factors (FGFb and FGFa) were determined using an enzyme-linked immunosorbent assay. RESULTS In patients with PsA, VEGF levels were positively correlated with CRP (P = 0.04), BASFI (P = 0.03), and disease duration (P = 0.007). No differences were found between patients with and without nail psoriaris in the VEGF or EGF levels (P = 0.32 and P = 0.85, respectively). There were no differences between patients with the peripheral and axial forms of arthritis in VEGF or EGF levels (P = 0.56 and P = 0.28, respectively). No significant correlations were observed between EGF and FGF levels and clinical presentation in patients with PsA. In patients with SAPHO, no significant correlations were found between angiogenic cytokine levels and clinical presentation. CONCLUSIONS Our data suggest a role of VEGF in the pathogenesis of PsA. Further studies are required to better understand the role of angiogenic cytokines in PsA.
引用
收藏
页码:297 / 302
页数:6
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