Abstract

BackgroundOne of the main causes of anaemia in patients with end-stage renal disease is relative deficiency in erythropoietin production. Eythropoiesis stimulating agent (ESA), a potent haematopoietic growth factor, is used to treat anaemia in haemodialysis patients. The effect of ESA is usually assessed by haematological indices such as red blood cell count, haemoglobin concentration and haematocrit, but erythrocyte indices do not provide information of the rapid change in erythropoietic activity. As erythrocyte creatine directly assess erythropoiesis, the aim of this study was to evaluate the effect of ESA in haemodialysis patients by measuring the erythrocyte creatine content.MethodsESA dose was fixed 3 months prior to the enrollment and was maintained throughout the entire study period. Erythrocyte creatine was measured with haematologic indices in 83 haemodialysis patients. Haemoglobin was also measured 3 months after.ResultsESA dose (152.4 ± 62.9 vs. 82.2 ± 45.5 units/kg/week, P = 0.0001) and erythrocyte creatine (2.07 ± 0.73 vs. 1.60 ± 0.41 μmol/gHb, p = 0.0003) were significantly higher in 27 patients with haemoglobin <10 g/dL compared to 56 patients with haemoglobin ≥10 g/dL. There was a fair correlation between ESA dose and the concentration of creatine in the erythrocytes (r = 0.55, P < 0.0001). Increase in haemoglobin (>0.1 g/dL) was observed in 37 patients, whereas haemoglobin did not increase in 46 patients. Erythrocyte creatine levels were significantly higher in those patients with an increase in haemoglobin compared to those without (2.04 ± 0.64 vs. 1.52 ± 0.39 μmol/gHb, p < 0.0001). When 8 variables (ESA dose, erythropoietin resistance index, C-reactive protein, intact parathyroid hormone, iron supplementation, presence of anaemia, erythrocyte creatine and reticulocyte) were used in the multivariate logistic analysis, erythrocyte creatine levels emerged as the most important variable associated with increase in haemoglobin (Chi-square = 6.19, P = 0.01).ConclusionErythrocyte creatine, a useful marker of erythropoietic capacity, is a reliable marker to estimate ameliorative effectiveness of ESA in haemodialysis patients.

Highlights

  • One of the main causes of anaemia in patients with end-stage renal disease is relative deficiency in erythropoietin production

  • We attempted to evaluate the ameliorative effectiveness of Eythropoiesis stimulating agent (ESA) in patients undergoing maintenance haemodialysis by measuring erythrocyte creatine content

  • Study patients We evaluated 83 patients (57 men and 26 women, mean age of 74 years) aged ≥20 years who had been receiving maintenance haemodialysis 3 times a week for at least 6 months in the Dialysis Unit of Takarazuka Hospital

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Summary

Introduction

One of the main causes of anaemia in patients with end-stage renal disease is relative deficiency in erythropoietin production. As erythrocyte creatine directly assess erythropoiesis, the aim of this study was to evaluate the effect of ESA in haemodialysis patients by measuring the erythrocyte creatine content. Erythropoiesis stimulating agent (ESA), a potent haematopoietic growth factor, has been shown to be effective in correcting anaemia in chronic renal failure [2,3,4,5], but the response rate is variable because resistant factors of erythropoiesis such as iron deficiency, inflammation, aluminum intoxication, hyperparathyroidism, blood loss or bone marrow dysfunction are involved [5, 6]. In contrast to haemoglobin levels which take a relatively long time to increase, total reticulocyte count can assess rapid change in erythropoiesis [8, 9]. We attempted to evaluate the ameliorative effectiveness of ESA in patients undergoing maintenance haemodialysis by measuring erythrocyte creatine content

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