The Conundrum of Managing Anemia in Chronic Kidney Disease Patients on Dialysis with Associated Hemoglobinopathies- Perspective from a Single Nephrology Centre in North –Eastern India

S. Nayak-Rao
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Abstract

Anemia is a common complication in chronic kidney disease (CKD) and has been associated with a reduced quality of life [1] as well as worse survival [2] and increased morbidity and mortality [3]. The prevalence of anemia is more severe as the estimated glomerular filtration rate (eGFR) declines and is 8.4% at stage 1 to 53.4% at stage 5. Similar data is observed in a more recent paper by the CKD Prognosis Consortium which also observed an increased prevalence of anemia among diabetic patients, independent of eGFR and albuminuria [4]. In CKD patients, EPO deficiency starts early in the course of CKD and appears initially, when eGFR falls below 30ml/min/1.73m2, this deficiency becomes more severe [5]. This absolute EPO deficiency can be caused by a decrease EPO production and /or errors in EPO sensing. CKD produces an alteration in oxygen delivery to the kidneys and results in adaptation of renal tissue to consume less oxygen and subsequent maintenance of normal tissue oxygen gradient. As a consequence, prolyl-hydroxylase domain (PHD) enzymes which regulates HIF activity remain active, the HIF heterodimer is not formed and the EPO gene is not activated [6]. Some CKD patients may also present with a functional EPO deficiency or EPO resistance, where normal range. EPO levels co-exist with low hemoglobin levels indicating a blunted bone marrow response to endogenous and exogenous EPO. Mechanisms hypothesized for EPO resistance include presence of pro-inflammatory cytokines thought to induce apoptosis and down regulation of expression of EPO receptor.
慢性肾病透析伴血红蛋白病患者贫血管理难题——来自印度东北部单一肾病中心的视角
贫血是慢性肾脏疾病(CKD)的常见并发症,与生活质量下降[1]、生存恶化[2]、发病率和死亡率增加[3]有关。随着估计的肾小球滤过率(eGFR)下降,贫血的患病率更为严重,1期为8.4%,5期为53.4%。CKD预后协会(CKD Prognosis Consortium)最近发表的一篇论文也观察到类似的数据,该论文还观察到糖尿病患者中贫血的患病率增加,与eGFR和蛋白尿无关[4]。在CKD患者中,EPO缺乏症在病程早期就开始出现,当eGFR低于30ml/min/1.73m2时,EPO缺乏症更为严重[5]。这种绝对的促生成素缺乏可能是由促生成素产生减少和/或促生成素感应错误引起的。CKD会改变肾脏的氧气输送,导致肾组织适应消耗更少的氧气,并随后维持正常的组织氧梯度。因此,调节HIF活性的脯氨酸羟化酶结构域(prolyl-hydroxylase domain, PHD)酶保持活性,HIF异源二聚体不形成,EPO基因不激活[6]。一些CKD患者也可能表现为功能性EPO缺乏或EPO抵抗,在正常范围内。EPO水平与低血红蛋白水平共存,表明骨髓对内源性和外源性EPO的反应迟钝。EPO耐药的假设机制包括促炎细胞因子的存在,被认为是诱导细胞凋亡和EPO受体表达下调。
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