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A randomised comparative study of the short term clinical and biological effects of intravenous pulse methylprednisolone and infliximab in patients with active rheumatoid arthritis despite methotrexate treatment
  1. P Durez1,
  2. A Nzeusseu Toukap1,
  3. B R Lauwerys1,
  4. D H Manicourt1,
  5. P Verschueren2,
  6. R Westhovens2,
  7. J-P Devogelaer1,
  8. F A Houssiau1
  1. 1Rheumatology Department, Cliniques Universitaires Saint-Luc, Université catholique de Louvain, Belgium
  2. 2Rheumatology Department, UZ Gasthuisberg, Katholieke Universiteit Leuven, Belgium
  1. Correspondence to:
    Dr F A Houssiau
    Rheumatology Department, Cliniques Universitaires Saint-Luc, Université catholique de Louvain, Avenue Hippocrate, 10, B-1200 Bruxelles, Belgium; houssiauruma.ucl.ac.be

Abstract

Objectives: To compare the short term clinical and biological effects of intravenous (IV) pulse methylprednisolone (MP) and infliximab (IFX) in patients with severe active rheumatoid arthritis (RA) despite methotrexate (MTX) treatment.

Methods: Patients with active RA despite MTX treatment were randomly allocated to receive a single IV infusion of MP (1 g) or three IV infusions of IFX (3 mg/kg) on weeks 0, 2, and 6. Patients were “blindly” evaluated for disease activity measures. Quality of life (QoL) was evaluated through the SF-36 health survey. Serum matrix metalloproteinase-3 (MMP-3) titres were measured at baseline, weeks 2 and 6.

Results: Compared with baseline, significant improvement was noted in all activity measures, including serum C reactive protein (CRP) titres, in the IFX group only. At week 14, 6/9 (67%) and 4/9 (44%) IFX patients met the ACR20 and 50 response criteria, while this was the case in only 1/12 (8%) and 0/12 (0%) MP patients, respectively (p<0.05). None of the QoL scales improved with MP treatment, whereas some did so in the IFX group. Serum MMP-3 titres significantly decreased (41% drop) at week 6 in the IFX group, while no changes were seen in patients given MP.

Conclusion: This short term randomised comparative study demonstrates that TNF blockade is better than MP pulse therapy in a subset of patients with severe refractory RA, with improvement in not only clinical parameters of disease activity but also biological inflammatory indices, such as serum CRP and MMP-3 titres.

  • ACR, American College of Rheumatology
  • CRP, C reactive protein
  • DMARD, disease modifying antirheumatic drug
  • IFX, infliximab
  • IL, interleukin
  • IV, intravenous
  • MMP, matrix metalloproteinase
  • MP, methylprednisolone
  • MTX, methotrexate
  • RA, rheumatoid arthritis
  • SJC, swollen joint count
  • TJC, tender joint count
  • TNF, tumour necrosis factor
  • rheumatoid arthritis
  • glucocorticoids
  • pulse therapy
  • infliximab
  • tumour necrosis factor blockade

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