Efficacy of sulfasalazine in patients with inflammatory back pain due to undifferentiated spondyloarthritis and early ankylosing spondylitis:: a multicentre randomised controlled trial

被引:120
作者
Braun, J.
Zochling, J.
Baraliakos, X.
Alten, R.
Burmester, G.
Grasedyck, K.
Brandt, J.
Haibel, H.
Hammer, M.
Krause, A.
Mielke, F.
Tony, H-P
Ebner, W.
Goemoer, B.
Hermann, J.
Zeidler, H.
Beck, E.
Baumgaertner, M.
Sieper, J.
机构
[1] Rheumazentrum Ruhrgebiet, D-44652 Herne, Germany
[2] Schlosspk Klin, Berlin, Germany
[3] Charite, Berlin, Germany
[4] Univ Hamburg, Hosp Eppendorf, D-20246 Hamburg, Germany
[5] Rheumatol Gemeinschaftspraxis, Berlin, Germany
[6] St Josefs Sendenhorst, Dept Rheumatol, Senderhorst, Germany
[7] Immanuel Hosp, Berlin, Germany
[8] Rheumatol Praxis, Berlin, Germany
[9] Univ Wurzburg, D-97070 Wurzburg, Germany
[10] Lainz Hosp, Dept Internal Med 2, A-1130 Vienna, Austria
[11] Polyclin Hospitaller Brothers St John God, Budapest, Hungary
[12] Graz Univ, Dept Internal Med, Div Rheumatol, Graz, Austria
[13] Leibniz Univ Hannover, Dept Rheumatol, D-30167 Hannover, Germany
[14] Anfomed GmbH, Erlangen, Germany
[15] Pfizer GmbH, Karlsruhe, Germany
关键词
D O I
10.1136/ard.2006.052878
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: To assess the effect of sulfasalazine (SSZ) on inflammatory back pain (IBP) due to active sundifferentiated spondyloarthritis (uSpA) or ankylosing spondylitis in patients with symptom duration < 5 years. Methods: Patients with IBP and a Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) > 3 from 12 centres were randomly assigned to 24 weeks' treatment with SSZ 2 g/day or placebo. The primary outcome variable was the change in BASDAI over 6 months. Secondary outcomes included measures of spinal pain, physical function and inflammation. Results: 230 patients (50% men, age range 18-64 years, 67% human leucocyte antigen B27 positive) were treated with either SSZ 2 x 1 g/day or placebo for 6 months. Enthesitis was found in 50%, and peripheral arthritis in 47% of the patients. The mean (SD) BASDAI dropped markedly in both groups: by 3.7 (2.7) and 3.8 (2.4), respectively, as did most secondary outcome measures. No noticeable difference in treatment was observed between groups. Patients with IBP and no peripheral arthritis had significantly (p = 0.03) more benefit with SSZ (BASDAI 5.1 (1.3) to 2.8 (2.3)) than with placebo (5.2 (1.6) to 3.8 (2.4)). Spinal pain (p = 0.03) and morning stiffness (p = 0.05) improved with SSZ in these patients, but other secondary outcomes were not markedly different. Conclusion: SSZ was no better than placebo for the treatment of the signs and symptoms of uSpA; however, SSZ was more effective than placebo in the subgroup of patients with IBP and no peripheral arthritis.
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收藏
页码:1147 / 1153
页数:7
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