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A Multicenter Study of the Predictive Value of Crescents in IgA Nephropathy

医学 免疫抑制 危险系数 四分位间距 肾病 回顾性队列研究 蛋白尿 内科学 置信区间 胃肠病学 泌尿科 内分泌学 糖尿病
作者
Mark Haas,Jacobien C. Verhave,Zhihong Liu,Charles E. Alpers,Jonathan Barratt,Jan U. Becker,Daniel C. Cattran,H. Terence Cook,Rosanna Coppo,John Feehally,Antonello Pani,Agnieszka Perkowska‐Ptasińska,S. A. Roberts,Maria Fernanda Soares,Hernán Trimarchi,Suxia Wang,Yukio Yuzawa,Hong Zhang,Stéphan Troyanov,Ritsuko Katafuchi
出处
期刊:Journal of The American Society of Nephrology 卷期号:28 (2): 691-701 被引量:289
标识
DOI:10.1681/asn.2016040433
摘要

The Oxford Classification of IgA nephropathy does not account for glomerular crescents. However, studies that reported no independent predictive role of crescents on renal outcomes excluded individuals with severe renal insufficiency. In a large IgA nephropathy cohort pooled from four retrospective studies, we addressed crescents as a predictor of renal outcomes and determined whether the fraction of crescent-containing glomeruli associates with survival from either a ≥50% decline in eGFR or ESRD (combined event) adjusting for covariates used in the original Oxford study. The 3096 subjects studied had an initial mean±SD eGFR of 78±29 ml/min per 1.73 m 2 and median (interquartile range) proteinuria of 1.2 (0.7–2.3) g/d, and 36% of subjects had cellular or fibrocellular crescents. Overall, crescents predicted a higher risk of a combined event, although this remained significant only in patients not receiving immunosuppression. Having crescents in at least one sixth or one fourth of glomeruli associated with a hazard ratio (95% confidence interval) for a combined event of 1.63 (1.10 to 2.43) or 2.29 (1.35 to 3.91), respectively, in all individuals. Furthermore, having crescents in at least one fourth of glomeruli independently associated with a combined event in patients receiving and not receiving immunosuppression. We propose adding the following crescent scores to the Oxford Classification: C0 (no crescents); C1 (crescents in less than one fourth of glomeruli), identifying patients at increased risk of poor outcome without immunosuppression; and C2 (crescents in over one fourth of glomeruli), identifying patients at even greater risk of progression, even with immunosuppression.
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