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本文引用的文献

1
Mechanisms of tubulointerstitial fibrosis.肾小管间质纤维化的机制。
J Am Soc Nephrol. 2010 Nov;21(11):1819-34. doi: 10.1681/ASN.2010080793. Epub 2010 Sep 23.
2
Erythropoietic response and outcomes in kidney disease and type 2 diabetes.肾脏疾病和 2 型糖尿病患者的红细胞生成反应和结局。
N Engl J Med. 2010 Sep 16;363(12):1146-55. doi: 10.1056/NEJMoa1005109.
3
Prevalence and management of anaemia in renal transplant recipients: data from ten European centres.肾移植受者贫血的患病率和管理:来自十个欧洲中心的数据。
Nephron Clin Pract. 2011;117(2):c127-34. doi: 10.1159/000319660. Epub 2010 Aug 6.
4
High dose epoetin beta in the first weeks following renal transplantation and delayed graft function: Results of the Neo-PDGF Study.肾移植后最初几周内使用高剂量促红细胞生成素β和延迟移植物功能:Neo-PDGF 研究的结果。
Am J Transplant. 2010 Jul;10(7):1695-700. doi: 10.1111/j.1600-6143.2010.03142.x.
5
Target haemoglobin to aim for with erythropoiesis-stimulating agents: a position statement by ERBP following publication of the Trial to reduce cardiovascular events with Aranesp therapy (TREAT) study.针对红细胞生成刺激剂的目标血红蛋白:在 Aranesp 治疗降低心血管事件试验(TREAT)研究发表后,ERBP 的立场声明。
Nephrol Dial Transplant. 2010 Sep;25(9):2846-50. doi: 10.1093/ndt/gfq336. Epub 2010 Jun 29.
6
Pathogenesis of tubulointerstitial fibrosis in chronic allograft dysfunction.慢性移植肾失功中肾小管间质性纤维化的发病机制。
Clin Transplant. 2009 Dec;23 Suppl 21:26-32. doi: 10.1111/j.1399-0012.2009.01106.x.
7
A trial of darbepoetin alfa in type 2 diabetes and chronic kidney disease.阿法达贝泊汀治疗2型糖尿病和慢性肾病的一项试验。
N Engl J Med. 2009 Nov 19;361(21):2019-32. doi: 10.1056/NEJMoa0907845. Epub 2009 Oct 30.
8
Mortality in renal transplant recipients given erythropoietins to increase haemoglobin concentration: cohort study.给予促红细胞生成素以提高血红蛋白浓度的肾移植受者的死亡率:队列研究。
BMJ. 2009 Oct 23;339:b4018. doi: 10.1136/bmj.b4018.
9
Negative effects of anemia on quality of life and its improvement by complete correction of anemia by administration of recombinant human erythropoietin in posttransplant patients.贫血对生活质量的负面影响以及通过给予重组人促红细胞生成素完全纠正移植后患者贫血来改善生活质量的情况。
Clin Exp Nephrol. 2009 Aug;13(4):355-360. doi: 10.1007/s10157-009-0170-x. Epub 2009 Apr 8.
10
Anaemia management in patients with chronic kidney disease: a position statement by the Anaemia Working Group of European Renal Best Practice (ERBP).慢性肾脏病患者的贫血管理:欧洲肾脏最佳实践(ERBP)贫血工作组的立场声明
Nephrol Dial Transplant. 2009 Feb;24(2):348-54. doi: 10.1093/ndt/gfn653. Epub 2008 Nov 26.

纠正肾移植后贫血可减缓移植肾肾病进展。

Correction of postkidney transplant anemia reduces progression of allograft nephropathy.

机构信息

Nephrology, Dialysis, Transplantation and Intensive Care Department, Centre Hospitalier Universitaire (CHU) Amiens, Hôpital Sud, ERI-12 Institut National de la Santé et de la Recherche Médicale, Jules Verne University, 80054 Amiens Cedex 1, France.

出版信息

J Am Soc Nephrol. 2012 Feb;23(2):360-8. doi: 10.1681/ASN.2011060546. Epub 2011 Dec 22.

DOI:10.1681/ASN.2011060546
PMID:22193388
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3269184/
Abstract

Retrospective studies suggest that chronic allograft nephropathy might progress more rapidly in patients with post-transplant anemia, but whether correction of anemia improves renal outcomes is unknown. An open-label, multicenter, randomized controlled trial investigated the effect of epoetin-β to normalize hemoglobin values (13.0-15.0 g/dl, n=63) compared with partial correction of anemia (10.5-11.5 g/dl, n=62) on progression of nephropathy in transplant recipients with hemoglobin <11.5 g/dl and an estimated creatinine clearance (eCrCl) <50 ml/min per 1.73 m(2). After 2 years, the mean hemoglobin was 12.9 and 11.3 g/dl in the normalization and partial correction groups, respectively (P<0.001). From baseline to year 2, the eCrCl decreased by a mean 2.4 ml/min per 1.73 m(2) in the normalization group compared with 5.9 ml/min per 1.73 m(2) in the partial correction group (P=0.03). Furthermore, fewer patients in the normalization group progressed to ESRD (3 versus 13, P<0.01). Cumulative death-censored graft survival was 95% and 80% in the normalization and partial correction groups, respectively (P<0.01). Complete correction was associated with a significant improvement in quality of life at 6 and 12 months. The number of cardiovascular events was low and similar between groups. In conclusion, this prospective study suggests that targeting hemoglobin values ≥13 g/dl reduces progression of chronic allograft nephropathy in kidney transplant recipients.

摘要

回顾性研究表明,移植后贫血的患者慢性移植肾肾病可能进展得更快,但纠正贫血是否能改善肾脏结局尚不清楚。一项开放标签、多中心、随机对照试验研究了促红细胞生成素-β将血红蛋白值正常化(13.0-15.0 g/dl,n=63)与部分纠正贫血(10.5-11.5 g/dl,n=62)对血红蛋白<11.5 g/dl 和估计肌酐清除率(eCrCl)<50 ml/min per 1.73 m(2)的移植受者肾病进展的影响。2 年后,正常化组和部分纠正组的平均血红蛋白分别为 12.9 和 11.3 g/dl(P<0.001)。与部分纠正组相比,正常化组从基线到第 2 年 eCrCl 平均下降 2.4 ml/min per 1.73 m(2)(P=0.03)。此外,正常化组进展为 ESRD 的患者较少(3 例与 13 例,P<0.01)。正常化组和部分纠正组的累积死亡-censored 移植物存活率分别为 95%和 80%(P<0.01)。正常化组在 6 个月和 12 个月时的生活质量显著改善。心血管事件的数量较低,两组之间相似。总之,这项前瞻性研究表明,将血红蛋白值目标值设定为≥13 g/dl 可减少肾移植受者慢性移植肾肾病的进展。