TY - JOUR ID - TI - TREATMENT OF RHEUMATOID ARTHRITIS IN BASRAH: CLINICAL EFFICACY AND TOXICITY OF METHOTREXATE USED ALONE OR IN COMBINATION WITH DICLOFENAC SODIUM AU - Abdullnasir H. Abdullah AU - Abdullah M. Jawad AU - Bassim N. Abood PY - 2009 VL - 27 IS - 2 SP - 84 EP - 89 JO - The Medical Journal of Basrah University المجلة الطبية لجامعة البصرة SN - 02530759 AB - ABSTRACTBackground: The present study is based on two assumptions. First is the racial and ethnic differences in thepresentation of rheumatoid arthritis (RA) and its response to drugs. And the second is the interaction betweennonsteroidal 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 treatmentof RA.Methods:Design: A three month randomized comparative clinical trialSetting: 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 singleweekly dose). Group II: received MTX single weekly dose plus diclofenac sodium 100 SR tablets once dailyMeasurements and evaluationPain, morning stiffness, joint function (number of the swollen and tender joints), patients and physician globalassessment, radiological evaluation (according to modified Sharp score for joint space narrowing and erosions), ACRcriteria for progression and remission of RA, laboratory findings (complete blood picture and ESR, blood groups, Hbelectrophoresis, 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 ascited 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 betime dependent. The average percent improvement in six clinical parameters mounted to about 35% compared to thebaseline measurements. The 20% improvement at 12 weeks of treatment using ACR criteria involved 42.8% ofpatients. Radiological findings (joint space narrowing and erosion) increased slightly by only 5.7% over the 12 weektreatment period. No significant change in all laboratory parameters measured. No important side effects peculiar toMTX could be figured out. Concurrent administration of diclofenac (sustained release formulation) with MTXresulted in a paradoxical finding. Instead of enhancing efficacy or toxicity of MTX, diclofenac reduced the efficacy ofMTX from 35.25% to only 15.78% at the end of the treatment period. The two groups, however, differed in someaspects e.g. disease duration and severity, and the type of blood groups which might possibly have contributed to thisdifference. The ACR20 in the combination group is 36.3% (compared to 42.8% in MTX group). Radiological findingsprogressed by 48.3% in the joint space narrowing and erosion. When results of MTX and MTX+diclofenac groupswere analyzed according to disease severity and blood groups, it was found that the response of patients with severebut not moderate disease was comparable in the two groups. Blood group (A) seems to be associated with enhancedresponse 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 the12 week treatment period. The drug seems to be well tolerated with no important adverse effects. In contrast to whatis expected, sustained formulation of diclofenac sodium reduced the efficacy of MTX. The latter finding, if proved tobe true, could have an important clinical implication.

ER -