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Comparison of steroid-pulse therapy and combined with mizoribine in IgA nephropathy: a randomized controlled trial
Comparison of steroid-pulse therapy and combined with mizoribine in IgA nephropathy: a randomized controlled trial
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Comparison of steroid-pulse therapy and combined with mizoribine in IgA nephropathy: a randomized controlled trial
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Comparison of steroid-pulse therapy and combined with mizoribine in IgA nephropathy: a randomized controlled trial
Comparison of steroid-pulse therapy and combined with mizoribine in IgA nephropathy: a randomized controlled trial

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Comparison of steroid-pulse therapy and combined with mizoribine in IgA nephropathy: a randomized controlled trial
Comparison of steroid-pulse therapy and combined with mizoribine in IgA nephropathy: a randomized controlled trial
Journal Article

Comparison of steroid-pulse therapy and combined with mizoribine in IgA nephropathy: a randomized controlled trial

2016
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Overview
Background The significance of immunosuppressants as an adjunct treatment with corticosteroids for IgA nephropathy (IgAN) has not been well demonstrated. This study was performed to compare two treatment regimens, steroid-pulse therapy or combined with mizoribine (MZR) in progressive IgAN. Methods Study design was a prospective randomized controlled trial of 40 patients with moderate to severe glomerular injuries who were randomly administered either pulse methylprednisolone followed by a 25-month course of oral prednisolone (P group, n  = 20) or in combination with MZR (150 mg/day for 24 months, M + P group, n  = 20). The primary endpoint was a reduction of proteinuria by ≥50 % of the baseline value. Secondary endpoints were increased serum creatinine (Cr) by ≥50 %, or a decrease in estimated glomerular filtration rate by ≤50 %. Results Twenty-five months after the initiation of treatment, urinary protein excretion significantly declined from the median of 0.98 to 0.17 g/gCr in the P group ( P  < 0.05) and from 1.01 to 0.38 g/gCr in the M + P group ( P  < 0.05). There was no statistical difference in the serial changes of proteinuria between two groups ( P  = 0.81). All patients reached the primary endpoint, and the cumulative incidence of the reduction of proteinuria was not significantly different ( P  = 0.76). No patient reached the secondary endpoint during the 25 months of treatment. Conclusions Both therapeutic regimens significantly reduced the levels of proteinuria. We could not find the additional effect of MZR in combination with steroid-pulses in this small-scale controlled trial. Steroid-pulse therapy with a 25-month course of oral steroids seems to be effective for progressive IgAN.