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本文引用的文献

1
Histopathologic features aid in predicting risk for progression of IgA nephropathy.组织病理学特征有助于预测 IgA 肾病进展的风险。
Clin J Am Soc Nephrol. 2010 Mar;5(3):425-30. doi: 10.2215/CJN.06530909. Epub 2010 Jan 14.
2
Prehypertension: epidemiology, consequences and treatment.高血压前期:流行病学、后果与治疗。
Nat Rev Nephrol. 2010 Jan;6(1):21-30. doi: 10.1038/nrneph.2009.191. Epub 2009 Nov 17.
3
Errors induced by indexing glomerular filtration rate for body surface area: reductio ad absurdum.用体表面积校正肾小球滤过率所导致的错误:归谬法
Nephrol Dial Transplant. 2009 Dec;24(12):3593-6. doi: 10.1093/ndt/gfp431. Epub 2009 Sep 3.
4
The Oxford classification of IgA nephropathy: rationale, clinicopathological correlations, and classification.IgA肾病的牛津分类:基本原理、临床病理相关性及分类
Kidney Int. 2009 Sep;76(5):534-45. doi: 10.1038/ki.2009.243. Epub 2009 Jul 1.
5
The Oxford classification of IgA nephropathy: pathology definitions, correlations, and reproducibility.IgA肾病的牛津分类:病理定义、相关性及可重复性。
Kidney Int. 2009 Sep;76(5):546-56. doi: 10.1038/ki.2009.168. Epub 2009 Jul 1.
6
Efficacy and safety of glucocorticoids therapy for IgA nephropathy: a meta-analysis of randomized controlled trials.糖皮质激素治疗IgA肾病的疗效与安全性:一项随机对照试验的荟萃分析
Am J Nephrol. 2009;30(4):315-22. doi: 10.1159/000226129. Epub 2009 Jun 23.
7
A scoring system to predict renal outcome in IgA nephropathy: a nationwide 10-year prospective cohort study.预测IgA肾病肾脏结局的评分系统:一项全国性的10年前瞻性队列研究。
Nephrol Dial Transplant. 2009 Oct;24(10):3068-74. doi: 10.1093/ndt/gfp273. Epub 2009 Jun 10.
8
Risk stratification for progression of IgA nephropathy using a decision tree induction algorithm.使用决策树归纳算法对IgA肾病进展进行风险分层。
Nephrol Dial Transplant. 2009 Apr;24(4):1242-7. doi: 10.1093/ndt/gfn610. Epub 2008 Nov 17.
9
Combination therapy of prednisone and ACE inhibitor versus ACE-inhibitor therapy alone in patients with IgA nephropathy: a randomized controlled trial.泼尼松与血管紧张素转换酶抑制剂联合治疗对比单独使用血管紧张素转换酶抑制剂治疗IgA肾病患者:一项随机对照试验
Am J Kidney Dis. 2009 Jan;53(1):26-32. doi: 10.1053/j.ajkd.2008.07.029. Epub 2008 Oct 19.
10
Testing for causality and prognosis: etiological and prognostic models.因果关系与预后检测:病因学与预后模型
Kidney Int. 2008 Dec;74(12):1512-5. doi: 10.1038/ki.2008.416. Epub 2008 Aug 20.

预测 IgA 肾病患者发生透析或死亡的风险。

Predicting the risk for dialysis or death in IgA nephropathy.

机构信息

Nephrology, Dialysis, and Renal Transplantation Department, University North Hospital, 42055 Saint-Étienne Cedex 2, France.

出版信息

J Am Soc Nephrol. 2011 Apr;22(4):752-61. doi: 10.1681/ASN.2010040355. Epub 2011 Jan 21.

DOI:10.1681/ASN.2010040355
PMID:21258035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3065230/
Abstract

For the individual patient with primary IgA nephropathy (IgAN), it remains a challenge to predict long-term outcomes for patients receiving standard treatment. We studied a prospective cohort of 332 patients with biopsy-proven IgAN patients followed over an average of 13 years. We calculated an absolute renal risk (ARR) of dialysis or death by counting the number of risk factors present at diagnosis: hypertension, proteinuria ≥1 g/d, and severe pathologic lesions (global optical score, ≥8). Overall, the ARR score allowed significant risk stratification (P < 0.0001). The cumulative incidence of death or dialysis at 10 and 20 years was 2 and 4%, respectively, for ARR=0; 2 and 9% for ARR=1; 7 and 18% for ARR=2; and 29 and 64% for ARR=3, in adequately treated patients. When achieved, control of hypertension and reduction of proteinuria reduced the risk for death or dialysis. In conclusion, the absolute renal risk score, determined at diagnosis, associates with risk for dialysis or death.

摘要

对于接受标准治疗的原发性 IgA 肾病 (IgAN) 患者个体,预测其长期预后仍然是一个挑战。我们研究了一组前瞻性队列的 332 名活检证实的 IgAN 患者,平均随访 13 年。我们通过计算诊断时存在的风险因素(高血压、蛋白尿≥1g/d 和严重的病理损伤(全球光学评分,≥8))的数量来计算绝对肾脏风险 (ARR)。总体而言,ARR 评分可显著进行风险分层 (P<0.0001)。在充分治疗的患者中,ARR=0 的患者在 10 年和 20 年时的死亡或透析累积发生率分别为 2%和 4%;ARR=1 的患者分别为 2%和 9%;ARR=2 的患者分别为 7%和 18%;ARR=3 的患者分别为 29%和 64%。当实现时,控制高血压和减少蛋白尿可降低死亡或透析的风险。总之,诊断时确定的绝对肾脏风险评分与透析或死亡风险相关。