Wu Henry H L, Chinnadurai Rajkumar
Department of Renal Medicine, Lancashire Teaching Hospitals NHS Foundation Trust, Preston, United Kingdom.
Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, United Kingdom.
Kidney Dis (Basel). 2022 Jan 14;8(2):103-114. doi: 10.1159/000521162. eCollection 2022 Mar.
Erythropoietin-stimulating agent (ESA) hyporesponsiveness is commonly observed in patients with anemia secondary to chronic kidney disease (CKD). Because of its complexity, a global consensus on how we should define ESA hyporesponsiveness remains unavailable. The reported prevalence and demographic information on ESA hyporesponsiveness within the CKD population are variable with no consensus definition.
ESA hyporesponsiveness is defined as having no increase in hemoglobin concentration from baseline after the first month of treatment on appropriate weight-based dosing. The important factors associated with ESA hyporesponsiveness include absolute or functional iron deficiency, inflammation, and uremia. Hepcidin has been demonstrated to play an important role in this process. Mineral bone disease secondary to CKD and non-iron malnutrition among other factors are also associated with ESA hyporesponsiveness. There is continued debate toward determining a gold-standard treatment pathway to manage ESA hyporesponsiveness. The development of hypoxia-inducing factor-stabilizers brings new insights and opportunities in the management of ESA hyporesponsiveness.
Management of ESA hyporesponsiveness involves a comprehensive multidisciplinary team approach to address its risk factors. The progression of basic and clinical research on identifying risk factors and management of ESA hyporesponsiveness brings greater hope on finding solutions to eventually tackling one of the most difficult problems in the topic of anemia in CKD.
促红细胞生成素刺激剂(ESA)低反应性在慢性肾脏病(CKD)继发贫血患者中普遍存在。由于其复杂性,目前对于如何定义ESA低反应性尚未达成全球共识。关于CKD人群中ESA低反应性的报道患病率和人口统计学信息各不相同,且没有统一的定义。
ESA低反应性定义为在基于体重的适当剂量治疗第一个月后血红蛋白浓度未较基线水平升高。与ESA低反应性相关的重要因素包括绝对或功能性缺铁、炎症和尿毒症。已证明铁调素在这一过程中起重要作用。CKD继发的矿物质骨病和非缺铁性营养不良等其他因素也与ESA低反应性有关。在确定管理ESA低反应性的金标准治疗途径方面仍存在持续争论。缺氧诱导因子稳定剂的开发为ESA低反应性的管理带来了新的见解和机会。
ESA低反应性的管理需要多学科综合团队方法来解决其危险因素。在识别ESA低反应性危险因素和管理方面的基础和临床研究进展,为最终找到解决CKD贫血这一最难题之一的方案带来了更大希望。