Effect of erythropoietin on urinary liver-type fatty-acid-binding protein in patients with chronic renal failure and anemia

Am J Nephrol. 2006;26(3):276-80. doi: 10.1159/000093934. Epub 2006 Jun 13.

Abstract

Background/aim: The urinary liver-type fatty-acid-binding protein (L-FABP) level reflects the clinical progression of chronic kidney disease. We conducted a study to determine whether administration of erythropoietin (EPO), which is produced in response to hypoxic stress, affects urinary protein excretion and L-FABP levels in patients with chronic renal failure (CRF) and anemia.

Methods: The study was an interventional trial that included 20 anemic CRF patients (median serum creatinine level 2.0 mg/dl, range 1.3-2.9 mg/dl; median hemoglobin concentration 9.2 g/dl, range 8.2-9.8 g/dl; median estimated glomerular filtration rate 20.5 ml/min, range 15.0-28.0 ml/min; group A). Recombinant EPO (12,000 U twice/month) was given to these patients for 6 months. Urinary protein, L-FABP, 8-hydroxy-2'-deoxyguanosine, and hemoglobin levels were measured before and 3 and 6 months after treatment. Twenty nonanemic CRF patients were enrolled as controls (group B).

Results: After 6 months, the hemoglobin level was increased as compared with the baseline level in group A treated with EPO (median 11.3 g/dl, range 9.3-13.8 g/dl, vs. median 9.2 g/dl, range 8.2-9.8 g/dl; p < 0.01) but not in the untreated group B (median 11.8 g/dl, range 10.2-13.0 g/dl, vs. median 12.1 g/dl, range 10.8-13.4 g/dl; not significant). The urinary protein excretion was decreased as compared with the baseline level in group A (median 1.2 g/day, range 0.6-1.9 g/day, vs. median 1.9 g/day, range 1.1-2.6 g/day; p < 0.01) but not in group B (median 1.4 g/day, range 0.7-2.2 g/day, vs. median 1.6 g/day, range 0.7-2.3 g/day; not significant). The urinary L-FABP level was also decreased as compared with the baseline level in group A (median 50.0 microg/g creatinine, range 7.5-90.0 microg/g creatinine, vs. median 115.0 microg/g creatinine, range 20.0-225.0 microg/g creatinine; p < 0.01) but not in group B (median 82.0 microg/g creatinine, range 15.5-158.0 microg/g creatinine, vs. median 76.0 microg/g creatinine, range 25.0-138.5 microg/g creatinine; not significant). The glomerular filtration rate changed little throughout the study period in either group. The urinary 8-hydroxy-2'-deoxyguanosine level was decreased as compared with the baseline level in group A (median 22.0 ng/mg creatinine, range 8.0-30.0 ng/mg creatinine, vs. median 38.5 ng/mg creatinine, range 14.0-68.0 ng/mg creatinine; p < 0.01) but not in group B (median 33.0 ng/mg creatinine, range 9.0-56.0 ng/mg creatinine, vs. median 30.0 ng/mg creatinine, range 10.0-54.0 ng/mg creatinine; not significant).

Conclusion: EPO supplementation may ameliorate renal tubular damage, in part, due to a reduction of oxidative stress in CRF patients with anemia.

Publication types

  • Controlled Clinical Trial

MeSH terms

  • Adult
  • Aged
  • Anemia / etiology
  • Anemia / prevention & control*
  • Anemia / urine*
  • Erythropoietin / therapeutic use*
  • Fatty Acid-Binding Proteins / urine*
  • Female
  • Hemoglobins / analysis*
  • Humans
  • Kidney Failure, Chronic / complications
  • Kidney Failure, Chronic / drug therapy*
  • Kidney Failure, Chronic / urine*
  • Male
  • Middle Aged
  • Recombinant Proteins
  • Treatment Outcome

Substances

  • FABP1 protein, human
  • Fatty Acid-Binding Proteins
  • Hemoglobins
  • Recombinant Proteins
  • Erythropoietin