TY - JOUR AU - Levin A. AU - LV Jicheng AU - Wang H. AU - Xu D. AU - Ma X. AU - Johnson D. AU - Zhang H. AU - Woodward Mark AU - Perkovic Vlado AB -
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
AD - Renal Division, Department of Medicine, Peking University First Hospital, Institute of Nephrology, No. 8, Xishiku Street, Xicheng District, Beijing 100034, China. hongzh@bjmu.edu.cn. AN - 22539830 BT - Journal of the American Society of Nephrology C2 - 3358763 DA - -35726387164 DP - NLM ET - 2012/04/28 LA - Eng M1 - 6 N1 - Lv, JichengXu, DaminPerkovic, VladoMa, XinxinJohnson, David WWoodward, MarkLevin, AdeeraZhang, HongWang, Haiyanfor the TESTING Study GroupJ Am Soc Nephrol. 2012 Jun;23(6):1108-1116. Epub 2012 Apr 26. N2 -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
PY - 2012 SN - 1533-3450 (Electronic)1046-6673 (Linking) SP - 1108 EP - 1116 T2 - Journal of the American Society of Nephrology TI - Corticosteroid Therapy in IgA Nephropathy VL - 23 ER -