TREATMENT OF RHEUMATOID ARTHRITIS IN BASRAH: CLINICAL EFFICACY AND TOXICITY OF METHOTREXATE USED ALONE OR IN COMBINATION WITH DICLOFENAC SODIUM

H. Abdullah, Abdullnasir; M. Jawad, Abdullah; N. Abood, Bassim

doi:10.33762/mjbu.2009.49178

	TREATMENT OF RHEUMATOID ARTHRITIS IN BASRAH: CLINICAL EFFICACY AND TOXICITY OF METHOTREXATE USED ALONE OR IN COMBINATION WITH DICLOFENAC SODIUM
The Medical Journal of Basrah University
Article 1, Volume 27, Issue 2, 2009, Pages 84-89 PDF (0 K)
DOI: 10.33762/mjbu.2009.49178
Authors
Abdullnasir H. Abdullah; Abdullah M. Jawad; Bassim N. Abood
Abstract
ABSTRACT Background: The present study is based on two assumptions. First is the racial and ethnic differences in the presentation of rheumatoid arthritis (RA) and its response to drugs. And the second is the interaction between nonsteroidal anti-inflammatory drugs (NSAIDs) and the disease modifying antirheumatic drugs (DMARDs) particularly methotrexate (MTX) with the possibility of enhanced toxicity. Objectives: to investigate the efficacy and toxicity of MTX alone or in combination with diclofenac in the treatment of RA. Methods: Design: A three month randomized comparative clinical trial Setting: Rheumatology Unit at the Teaching Hospital and the Department of Pharmacology, College of Medicine, University of Basrah, Basrah, Iraq. Patients: Patients with moderate to severe RA were classified into, Group I: received MTX (7.5 mg orally as a single weekly dose). Group II: received MTX single weekly dose plus diclofenac sodium 100 SR tablets once daily Measurements and evaluation Pain, morning stiffness, joint function (number of the swollen and tender joints), patients and physician global assessment, radiological evaluation (according to modified Sharp score for joint space narrowing and erosions), ACR criteria for progression and remission of RA, laboratory findings (complete blood picture and ESR, blood groups, Hb electrophoresis, AST, ALT, blood urea) and drug adverse effects were evaluated. Results: Twenty eight patients with moderate to severe RA were randomly allocated into two treatment groups as cited in the Methods. Only 25 patients managed to complete the 12 week treatment course. Oral MTX (7.5 mg) resulted in a statistically significant clinical improvement after 12 weeks of treatment. The improvement seems to be time dependent. The average percent improvement in six clinical parameters mounted to about 35% compared to the baseline measurements. The 20% improvement at 12 weeks of treatment using ACR criteria involved 42.8% of patients. Radiological findings (joint space narrowing and erosion) increased slightly by only 5.7% over the 12 week treatment period. No significant change in all laboratory parameters measured. No important side effects peculiar to MTX could be figured out. Concurrent administration of diclofenac (sustained release formulation) with MTX resulted in a paradoxical finding. Instead of enhancing efficacy or toxicity of MTX, diclofenac reduced the efficacy of MTX from 35.25% to only 15.78% at the end of the treatment period. The two groups, however, differed in some aspects e.g. disease duration and severity, and the type of blood groups which might possibly have contributed to this difference. The ACR20 in the combination group is 36.3% (compared to 42.8% in MTX group). Radiological findings progressed by 48.3% in the joint space narrowing and erosion. When results of MTX and MTX+diclofenac groups were analyzed according to disease severity and blood groups, it was found that the response of patients with severe but not moderate disease was comparable in the two groups. Blood group (A) seems to be associated with enhanced response and group (O) with a reduced one. Conclusion: Methotrexate 7.5 mg as a single oral dose per week produced a significant clinical improvement over the 12 week treatment period. The drug seems to be well tolerated with no important adverse effects. In contrast to what is expected, sustained formulation of diclofenac sodium reduced the efficacy of MTX. The latter finding, if proved to be true, could have an important clinical implication.

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