Document 0285 DOCN M9440285 TI Comparison of two glucocorticoid preparations (deflazacort and prednisone) in the treatment of immune-mediated diseases. DT 9404 AU Scudeletti M; Puppo F; Lanza L; Mantovani L; Bosco O; Iudice A; Imbimbo B; Indiveri F; Department of Internal Medicine, Clinical Methodology, University; of Genoa, Italy. SO Eur J Clin Pharmacol. 1993;45 Suppl 1:S29-34. Unique Identifier : AIDSLINE MED/94148037 AB Different glucocorticoid preparations modify the immune reaction in different ways. In this paper, the therapeutic efficacy of two glucocorticoids, deflazacort (DFZ) and prednisone (PDN), are discussed in relation to a group of 30 patients with systemic lupus erythematosus (n = 12) or rheumatoid arthritis (n = 18). The disease sub-groups were divided into two arms, one of which was treated with DFZ and one with PDN in a double-blind protocol. The results of this study indicate that DFZ and PDN induced a clinical remission within 1 month which was maintained until the 6th month. Nevertheless, certain immunological modifications, including a significant reduction of the circulating T lymphocyte level and of the CD4/CD8 ratio, which was between 1 and 1,5 during the DFC treatment and between 1 and 2 during the PDN treatment, are more pronounced and more stable with DFZ than with PDN. Moreover, DFZ has a smaller effect on calcium and glucose metabolism than PDN since the serum glucose and calcium level of patients treated with PDN increased respectively from 90 up to 130 mg/dl and from 9,5 to 11,5 mg/dl whereas those of patients treated with DFC remained within the normal range. These findings indicate that DFZ may have advantages over PDN in the treatment of immune-mediated diseases. DE Adult Anti-Inflammatory Agents, Steroidal/*THERAPEUTIC USE Arthritis, Rheumatoid/*DRUG THERAPY/IMMUNOLOGY Comparative Study CD4-CD8 Ratio/DRUG EFFECTS Double-Blind Method Human Lupus Erythematosus, Systemic/*DRUG THERAPY/IMMUNOLOGY Middle Age Prednisone/*THERAPEUTIC USE Pregnenediones/*THERAPEUTIC USE Remission Induction CLINICAL TRIAL JOURNAL ARTICLE RANDOMIZED CONTROLLED TRIAL SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).