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Impairment of phagocyte oxidative metabolism in hemodialyzed patients with iron overload.
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1986
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Iron MetabolismImmunologyWhole BloodIron DeficiencyRedox BiologyPmn ResponseOxidative StressInflammationAnemiaHemodialyzed PatientsBioanalysisHematologyClinical ChemistryChronic Kidney DiseaseHealth SciencesIron OverloadHeme SignalingHeme HomeostasisHeme DegradationPhysiologyChronic HemodialysisPhagocyte Oxidative MetabolismMetabolismMedicineNephrologyHepcidin
In order to study the influence of iron overload on the polymorphonuclear leucocyte (PMN) metabolism of patients on chronic hemodialysis, generation of superoxide anion (O2-) by PMN in whole blood was compared in two groups of hemodialyzed patients: group A consisted of twenty-one individuals with serum ferritin levels above 1000 ng/ml and group B of nineteen individuals with serum ferritin levels below 1000 ng/ml. Whereas basal production of O2- was similar in the two groups (6.3 +/- 4.6 vs 11.5 +/- 8.3 nmoles O2- 10(6) granulocytes-1 15 min-1) (mean +/- s.e.m.), PMN response to opsonized zymosan was significantly lower in group A as compared with group B (86.5 +/- 6.3 vs 120.4 +/- 8.2 nmoles O2- 10(6) granulocytes-1 15 min-1) (p less than 0.01). Superoxide anion generation induced by the dialysis procedure was reduced in eight patients from group A (89.2 +/- 32.1) as compared with eight patients from group B (374.3 +/- 100.0 nmoles O2- 10(6) granulocytes-1 15 min-1) (p less than 0.05). These data suggest that iron overload may be involved in the impairment of neutrophil phagocytosis in patients on chronic hemodialysis.