Oxidative stress from rapid versus slow intravenous iron replacement in haemodialysis patients

Methods and Results:  Oxidative stress was examined in 19 erythropoietin‐treated haemodialysis patients who were receiving 100 mg of iron sucrose every 2 weeks by two intravenous methods, rapid injection and slow infusion. There were no significant differences in incidence of iron oversaturation state between the two methods. Regarding oxidative stress markers, the values of plasma and red blood cell thiobarbituric acid reactive substances (TBARS) expressed in terms of malonyldialdehyde (MDA) equivalents following the two methods did not increase, and the values of area under the curve (AUC) of both markers were not different between both regimens. Also, there were no significant differences in the values of plasma and AUC of anti‐oxidant markers including total anti‐oxidant status, reduced thiols, and vitamin E among both periods treated with two intravenous iron methods.

[1]  C. Chaimovitz,et al.  Induction of protein oxidation by intravenous iron in hemodialysis patients: role of inflammation. , 2002, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[2]  Peter Stenvinkel,et al.  The elephant in uremia: oxidant stress as a unifying concept of cardiovascular disease in uremia. , 2002, Kidney international.

[3]  A. Carrington,et al.  A free radical. , 2020, Annual review of physical chemistry.

[4]  M. Nava,et al.  Melatonin prevents oxidative stress resulting from iron and erythropoietin administration. , 2001, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[5]  C. Charytan,et al.  Efficacy and safety of iron sucrose for iron deficiency in patients with dialysis-associated anemia: North American clinical trial. , 2001, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[6]  Z. Massy,et al.  Oxidative stress and haemodialysis: role of inflammation and duration of dialysis treatment. , 2001, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[7]  M. Boaz,et al.  Secondary prevention with antioxidants of cardiovascular disease in endstage renal disease (SPACE): randomised placebo-controlled trial , 2000, The Lancet.

[8]  F. Ursini,et al.  Oxidant stress in hemodialysis: prevention and treatment strategies. , 2000, Kidney international. Supplement.

[9]  T. Miyata,et al.  Relevance of oxidative and carbonyl stress to long-term uremic complications. , 2000, Kidney international. Supplement.

[10]  C. Charytan,et al.  Safety and efficacy of iron sucrose in patients sensitive to iron dextran: North American clinical trial. , 2000, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[11]  J. Roob,et al.  Vitamin E attenuates oxidative stress induced by intravenous iron in patients on hemodialysis. , 2000, Journal of the American Society of Nephrology : JASN.

[12]  M. Boaz,et al.  Serum malondialdehyde and prevalent cardiovascular disease in hemodialysis. , 1999, Kidney international.

[13]  P. Stenvinkel,et al.  Apo(a)-isoform size, nutritional status and inflammatory markers in chronic renal failure. , 1998, Kidney international.

[14]  F. Brunner,et al.  [Parenteral iron therapy: problems and possible solutions]. , 1998, Schweizerische medizinische Wochenschrift.

[15]  I. Macdougall,et al.  A randomized controlled study of iron supplementation in patients treated with erythropoietin. , 1996, Kidney international.

[16]  G. Jong,et al.  ‘Oversaturation’ of transferrin after intravenous ferric gluconate (FerrlecitR) in haemodialysis patients , 1996 .

[17]  H. Adriaansen,et al.  'Oversaturation' of transferrin after intravenous ferric gluconate (Ferrlecit(R)) in haemodialysis patients. , 1996, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[18]  M. Perazella Reduction in recombinant human erythropoietin doses by the use of chronic intravenous iron supplementation. , 1995, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[19]  C. Combe,et al.  Evaluation of red blood cell lipoperoxidation in hemodialysed patients during erythropoietin therapy supplemented or not with iron. , 1995, Nephron.

[20]  H. Danielsen,et al.  Intravenous iron-sucrose complex to reduce epoetin demand in dialysis patients , 1994, The Lancet.

[21]  M. Hu,et al.  Measurement of protein thiol groups and glutathione in plasma. , 1994, Methods in enzymology.

[22]  C. Rice-Evans,et al.  A novel method for measuring antioxidant capacity and its application to monitoring the antioxidant status in premature neonates. , 1993, Clinical science.

[23]  K. Mcleish,et al.  Polymorphonuclear leukocyte function during hemodialysis: relationship to complement activation. , 1989, Nephron.

[24]  R. D. Situnayake,et al.  The Use of Different Lipids to Express Serum Tocopherol: Lipid Ratios for the Measurement of Vitamin E Status , 1986, Annals of clinical biochemistry.

[25]  W. Lands,et al.  Selective microdetermination of lipid hydroperoxides. , 1985, Analytical biochemistry.