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      Mizoribine as a safe and effective combined maintenance therapy with prednisolone for anti-neutrophil cytoplasmic antibody-associated vasculitis in a hemodialysis patient

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          Abstract

          A 77-year-old man developed severe renal insufficiency due to proteinase 3 anti-neutrophil cytoplasmic antibody (PR3-ANCA)-associated vasculitis, and was started on hemodialysis (HD). Because his renal insufficiency appeared to be irreversible, he was maintained on oral prednisolone (PSL) at 5 mg/day. However, a disease flare-up with alveolar hemorrhage occurred. Serology revealed elevated levels of PR3-ANCA and C-reactive protein (CRP). The patient was given pulse therapy with a quarter dose of methylprednisolone (m-PSL) (250 mg, 3 days), followed by oral PSL at 15 mg/day. As a supplemental treatment, he was given 25 mg of mizoribine (MZR) immediately after each HD session. Subsequently, the levels of PR3-ANCA and CRP decreased, and the alveolar hemorrhage resolved. The dose of MZR to be given was determined by measuring the patient’s serum concentrations of MZR at various time points after the HD session. The maintenance dose of MZR was finally set at 50 mg. At present, the oral PSL dosage has been tapered to 10 mg/day, and the patient has achieved a state of remission without any side effects.

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          Most cited references22

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          BSR and BHPR guidelines for the management of adults with ANCA associated vasculitis.

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            A multicenter trial of mizoribine compared with placebo in children with frequently relapsing nephrotic syndrome.

            The use of corticosteroids or cytotoxic/immunosuppressive agents such as cyclophosphamide, chlorambucil, and cyclosporine for the treatment of frequently relapsing nephrotic syndrome (FRNS) is limited because of their adverse effects. This study was conducted to evaluate the efficacy and safety of mizoribine, a relatively new immunosuppressive drug developed in Japan, in children with FRNS. A double-blind, placebo-controlled, multicenter trial was carried out in children, from 2 to 19 years old, with FRNS. At relapse, patients were treated with prednisolone. According to a dynamic allocation, mizoribine or a placebo was concurrently administered to each patient. Prednisolone was gradually tapered and discontinued within 12 weeks. The test drug was maintained for 48 weeks. The primary end point was the relapse rate (the total number of relapses/the total treatment days for all patients). Analyses were performed according to the intention-to-treat principle. The primary analysis was conducted on 99 mizoribine- and 98 placebo-treated patients. The relapse rate was lower in the mizoribine group than in the placebo group (0.0055 vs. 0.0067; ratio 0.81, 95% CI, 0.61 to 1.05, P = 0.12). The hazard ratio of the cumulative remission rate between the two groups was 0.79 (95% CI, 0. 57 to 1.08). In the subgroups consisting of patients 10 years old or younger, the relapse rate ratio between the mizoribine subgroup (54 patients) and the placebo subgroup (57 patients) was 0.66 (95% CI, 0. 44 to 0.94, P = 0.017). The hazard ratio of the cumulative remission rate between the two subgroups was 0.56 (95% CI, 0.37 to 0.85, P = 0. 007). Hyperuricemia was the most common adverse event with mizoribine (16%), but was transient. Compared with the placebo, mizoribine significantly decreased the relapse rate and prolonged the remission period in the subgroup consisting of patients 10 years old or younger. This drug may be useful in young children with FRNS who generally relapse more frequently than older children.
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              Studies on bredinin. I. Isolation, characterization and biological properties.

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                Author and article information

                Contributors
                +81-254-223121 , +81-254-263874 , hisa-gen@ar.wakwak.com
                Journal
                CEN Case Rep
                CEN Case Rep
                CEN Case Reports
                Springer Japan (Tokyo )
                2192-4449
                30 January 2013
                30 January 2013
                November 2013
                : 2
                : 2
                : 139-143
                Affiliations
                [1 ]GRID grid.416211.1, Division of Nephrology, , Niigata Prefectural Shibata Hospital, ; 2-8, Motomachi 1-chome, Shibata, Niigata 957-8588 Japan
                [2 ]GRID grid.260975.f, ISNI 0000000106715144, Division of Clinical Nephrology and Rheumatology, , Niigata University Graduate School of Medical and Dental Sciences, ; 1-757 Asahimachi-dori, Cyuuou-ku, Niigata, 951-8510 Japan
                Article
                50
                10.1007/s13730-012-0050-1
                5418497
                22fbedcd-48c3-44ae-936c-715214772778
                © The Author(s) 2012
                History
                : 28 August 2012
                : 4 November 2012
                Categories
                Case Report
                Custom metadata
                © Japanese Society of Nephrology 2013

                mizoribine,hemodialysis,pulmonary hemorrhage,proteinase 3 anti-neutrophil cytoplasmic antibody-associated vasculitis

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