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促红细胞生成素治疗与血液透析患者髋部骨折风险。

Erythropoietin treatment and the risk of hip fractures in hemodialysis patients.

机构信息

Molecular Medicine Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.

National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

J Bone Miner Res. 2021 Jul;36(7):1211-1219. doi: 10.1002/jbmr.4297. Epub 2021 May 5.

Abstract

Erythropoietin (EPO) is the primary regulator of bone marrow erythropoiesis. Mouse models have provided evidence that EPO also promotes bone remodeling and that EPO-stimulated erythropoiesis is accompanied by bone loss independent of increased red blood cell production. EPO has been used clinically for three decades to treat anemia in end-stage renal disease, and notably, although the incidence of hip fractures decreased in the United States generally after 1990, it rose among hemodialysis patients coincident with the introduction and subsequent dose escalation of EPO treatment. Given this clinical paradox and findings from studies in mice that elevated EPO affects bone health, we examined EPO treatment as a risk factor for fractures in hemodialysis patients. Relationships between EPO treatment and hip fractures were analyzed using United States Renal Data System (USRDS) datasets from 1997 to 2013 and Consolidated Renal Operations in a Web-enabled Network (CROWNWeb) datasets for 2013. Fracture risks for patients treated with <50 units of EPO/kg/week were compared to those receiving higher doses by multivariable Cox regression. Hip fracture rates for 747,832 patients in USRDS datasets (1997-2013) increased from 12.0 per 1000 patient years in 1997 to 18.9 in 2004, then decreased to 13.1 by 2013. Concomitantly, average EPO doses increased from 11,900 units/week in 1997 to 18,300 in 2004, then decreased to 8,800 by 2013. During this time, adjusted hazard ratios for hip fractures with EPO doses of 50-149, 150-299, and ≥ 300 units/kg/week compared to <50 units/kg/week were 1.08 (95% confidence interval [CI], 1.01-1.15), 1.22 (95% CI, 1.14-1.31), and 1.41 (95% CI, 1.31-1.52), respectively. Multivariable analyses of 128,941 patients in CROWNWeb datasets (2013) replicated these findings. This study implicates EPO treatment as an independent risk factor for hip fractures in hemodialysis patients and supports the conclusion that EPO treatment may have contributed to changing trends in fracture incidence for these patients during recent decades. Published 2021. This article is a U.S. Government work and is in the public domain in the USA. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

摘要

促红细胞生成素 (EPO) 是调节骨髓中红细胞生成的主要调节剂。小鼠模型研究表明,EPO 还能促进骨重塑,EPO 刺激的红细胞生成伴随着独立于红细胞生成增加的骨丢失。促红细胞生成素已经在临床上用于治疗终末期肾病的贫血,值得注意的是,尽管美国的髋部骨折发病率在 1990 年后普遍下降,但随着促红细胞生成素治疗的引入和随后的剂量升级,血液透析患者的髋部骨折发病率上升。鉴于这一临床矛盾以及在小鼠研究中发现的促红细胞生成素升高对骨骼健康的影响,我们研究了促红细胞生成素治疗是否是血液透析患者骨折的一个风险因素。使用美国肾脏数据系统 (USRDS) 1997 年至 2013 年的数据和 2013 年的联合肾脏操作在网络启用网络 (CROWNWeb) 数据集分析了促红细胞生成素治疗与髋部骨折之间的关系。通过多变量 Cox 回归比较了每周接受 <50 单位/kg/体重的 EPO 治疗的患者与接受更高剂量 EPO 治疗的患者之间的骨折风险。USRDS 数据集中 747832 例患者(1997-2013 年)的髋部骨折发生率从 1997 年的每 1000 例患者 12.0 例增加到 2004 年的 18.9 例,然后在 2013 年下降到 13.1 例。与此同时,平均 EPO 剂量从 1997 年的每周 11900 单位增加到 2004 年的每周 18300 单位,然后在 2013 年下降到每周 8800 单位。在此期间,每周接受 50-149、150-299 和 ≥300 单位/kg/体重的 EPO 剂量与每周接受 <50 单位/kg/体重的 EPO 剂量相比,髋部骨折的调整后危险比分别为 1.08(95%置信区间 [CI],1.01-1.15)、1.22(95% CI,1.14-1.31)和 1.41(95% CI,1.31-1.52)。CROWNWeb 数据集(2013 年)中对 128941 例患者的多变量分析复制了这些发现。本研究表明,促红细胞生成素治疗是血液透析患者髋部骨折的一个独立危险因素,并支持促红细胞生成素治疗可能导致这些患者近年来骨折发病率变化的结论。2021 年出版。本文是美国政府的一项工作,在美国属于公有领域。由 Wiley 期刊出版公司代表美国骨矿研究协会 (ASBMR) 出版的《骨与矿物研究杂志》。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f69e/8360057/8f5b4354e9fe/JBMR-36-1211-g001.jpg

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