02218nas a2200241 4500000000100000008004100001260001700042100001300059700001500072700001200087700001000099700001000109700001500119700001300134700001800147700001900165245004600184250001500230300001400245490000700259520166400266020004601930 2012 d c-357263871641 aLevin A.1 aLV Jicheng1 aWang H.1 aXu D.1 aMa X.1 aJohnson D.1 aZhang H.1 aWoodward Mark1 aPerkovic Vlado00aCorticosteroid Therapy in IgA Nephropathy a2012/04/28 a1108-11160 v233 a

The benefits and risks of steroids for the treatment of IgA nephropathy remain uncertain. We systematically searched MEDLINE, EMBASE, and the Cochrane Library for randomized, controlled trials of corticosteroid therapy for IgA nephropathy published between 1966 and March 2011. We identified nine relevant trials that included 536 patients who had urinary protein excretion >1 g/d and normal renal function. Forty-six (8.6%) of these patients developed a kidney failure event, defined as doubling of the serum creatinine/halving of the GFR or ESRD. Overall, steroid therapy was associated with a lower risk for kidney failure (relative risk, 0.32 [95% confidence interval [CI], 0.15-0.67]; P=0.002) and a reduction in proteinuria (weighted mean difference, -0.46 g/d [95% CI, -0.63 to -0.29 g/d]), with no evidence of heterogeneity in these outcomes. Subgroup analysis suggested that the dose modifies the effect of steroids for renal protection (P for heterogeneity=0.030): Relatively high-dose and short-term therapy (prednisone >30 mg/d or high-dose pulse intravenous methylprednisolone with duration

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