[U wave in the electrocardiogram in children].
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Biomedical subjects
Publications and source records attributed to J Lewandowicz.
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OBJECTIVE: To evaluate the effect of methotrexate (MTX) in combination with prednizone on cytokine levels, acute phase proteins and thiobarbituric acid reactive substances (TBAR--an indicator of peroxidative damage to tissue lipids) in the blood of rheumatoid arthritis (RA) patients and to investigate their associations with clinical disease activity. METHODS: We measured blood concentrations of interleukin-1 beta (IL-1 beta), interleukin- 6 (IL-6), TBARs and classical clinical and laboratory indices of disease activity in 36 RA subjects before and after 3 and 6 month treatment with MTX and prednizone. Only RA subjects who stopped any disease-modifying anti rheumatic drugs treatment for last 3 months were included in the study. Baseline cytokine and TBARs levels were compared with those obtained with 20 healthy controls. RESULTS: Compared to controls RA subjects had elevated levels of circulating IL-1 beta (63.3 +/- 47.6 vs 13.7 +/- 7.8 pg/ml, p<0.01), IL-6 (147.2 +/- 76.5 vs 15.9 +/- 13.3 pg/ml, p<0.001) and TBARs (3.11 +/- 0.42 vs 1.34 +/- 0.45 nmol/1, p<0.001) concentrations. MTX in combination with prednizone improved patient clinical status that was accompanied by 1.96-, 1.25-, and 1.35-fold decrease in IL-1 beta, IL-6 and TBARs after 6 month treatment (p<0.001), respectively. Although, IL-1 and IL-6 revealed a few correlations with classical indices of disease activity no association was found between patient clinical status improvement and cytokine changes over 6 month treatment. CONCLUSIONS: MTX in combination with prednizone decreases blood levels of IL-1 beta and IL-6 and inhibits the intensity of free radical- mediated processes in RA subjects. Monitoring of plasma concentrations of these cytokines could not predict the treatment efficacy.
Thirty five patients with rheumatoid arthritis were given TFX Polfa, initially everyday in the intramuscular injections in the dose of 10 mg TFX protein for 60 days, followed by 1 injection of 10 mg TFX protein a week for 10 months. Other 30 patients with rheumatoid arthritis treated with gold salts were used for comparison. Several clinical and laboratory tests were performed before the treatment and after 1 year. A one-year therapy significantly improved all clinical parameters in both groups. A significant increase in hemoglobin and erythrocyte count was noted in patients treated with TFX. A significant decrease in the markers of inflammation was seen. A percentage of both early and delayed E rosettes increased highly significantly. The obtained results suggest that TFX Polfa is efficient in these cases of the rheumatoid arthritis which cannot be treated with gold salts.
Calf thymus preparation (TFX-Polfa) was administered + to 25 patients with classic rheumatoid arthritis in the II and III phase of the disease. Only patients not tolerating gold or D-penicillamine because of allergy or other complications, were included into the study. TFX was administered in a daily dose of 10 mg TFX protein i.m. for 60 consecutive days, followed by the treatment in outpatient clinic for successive++ 10 months. Statistically significant increase in the hemoglobin concentration and erythrocyte counts was produced by both a 2-month intensive treatment and a 12-month of therapy with TFX.