Abstract

BackgroundThe causes of anaemia in patients with end-stage renal disease include a relative deficiency in erythropoietin production and complex clinical conditions. We aimed to investigate the underlying mechanisms of anaemia in patients with end-stage renal disease who were undergoing maintenance dialysis by measuring erythrocyte creatine levels.MethodsIn a cross-sectional study, we evaluated 69 patients with end-stage renal disease who were receiving haemodialysis (n = 55) or peritoneal dialysis (n = 14). Erythrocyte creatine level, a quantitative marker of mean red blood cell (RBC) age, was measured.ResultsThe mean RBC age was significantly shorter in the haemodialysis group than in the peritoneal dialysis group (47.7 days vs. 59.8 days, p < 0.0001), although the haemoglobin levels were comparable between the groups. A Spearman correlation coefficient analysis revealed that shortened RBC age positively correlated with transferrin saturation (r = 0.54), ferritin level (r = 0.47), and haptoglobin level (r = 0.39) but inversely related with reticulocyte (r = − 0.36), weekly doses of erythropoiesis-stimulating agents (ESAs; r = − 0.62), erythropoietin resistance index (r = − 0.64), and intradialytic ultrafiltration rate (r = − 0.32).ConclusionsShortened RBC age was observed in patients who were receiving maintenance haemodialysis and was associated with iron deficiency, greater haptoglobin consumption, higher ESA requirements, and poor erythropoietin responsiveness, as well as with greater intradialytic fluid extraction.

Highlights

  • The causes of anaemia in patients with end-stage renal disease include a relative deficiency in erythropoietin production and complex clinical conditions

  • No significant difference in haemoglobin level was observed between the groups, the haemodialysis group had significantly lower transferrin saturation and ferritin levels than the peritoneal dialysis group

  • The weekly erythropoiesis-stimulating agents (ESAs) dose and erythropoietin resistance index were significantly higher in the haemodialysis group than in the peritoneal dialysis group

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Summary

Introduction

The causes of anaemia in patients with end-stage renal disease include a relative deficiency in erythropoietin production and complex clinical conditions. We aimed to investigate the underlying mechanisms of anaemia in patients with end-stage renal disease who were undergoing maintenance dialysis by measuring erythrocyte creatine levels. The causes of anaemia in end-stage renal disease include a relative deficiency in erythropoietin production and complex clinical conditions such as iron deficiency, inflammation, and haemolysis [2]. Compared with the 51Cr-labelling method, erythrocyte creatine is a simple, rapid, and economically favourable marker that can be measured using a single blood sample examination. We used erythrocyte creatine level to elucidate the incidence and underlying mechanisms associated with the development of anaemia in patients with end-stage renal disease who were receiving maintenance haemodialysis or peritoneal dialysis

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