PMID- 11728984 OWN - NLM STAT- MEDLINE DCOM- 20011213 LR - 20121115 IS - 1523-6838 (Electronic) IS - 0272-6386 (Linking) VI - 38 IP - 6 DP - 2001 Dec TI - Effects of erythropoietin and aminoguanidine on red blood cell deformability in diabetic azotemic and uremic patients. PG - 1414-20 AB - Impaired red blood cell-deformability (RBC-df) is noted in patients with diabetes and may play a role in the pathogenesis of microvasculopathy and nephropathy. We report the effects of erythropoietin (EPO) alone and combined with aminoguanidine (AG) for 1 year on RBC-df in predialysis patients (P-DPs) with renal insufficiency and in end-stage renal disease (ESRD) patients on maintenance hemodialysis (DPs). Nine P-DPs who received EPO 50 U/kg by subcutaneous injection 3 times per week are compared with 5 P-DPs treated without EPO (mean serum creatinine 4.1 +/- 0.1 versus 4.2 +/- 0.6 mg/dL, respectively). Twelve DPs (Kt/V = 1.5 +/- 0.1) were studied. Six DPs received AG 200 mg/every other day by mouth and EPO 50 U/kg by intravenous (IV) injection, and 6 DPs received EPO (50 U/kg) and placebo and served as control. RBC-df improved significantly in 9 P-DPs treated with EPO at 6 months (from 2.7 +/- 0.1 to 1.6 +/- 0.2, P = 0.005). This positive effect was sustained at 12 months (P = 0.005); there was no change in RBC-df in P-DPs receiving usual care without EPO. RBC-df improved significantly and progressively at 6 and 12 months in DPs treated with EPO and AG (from 2.2 +/- 0.2 to 1.8 +/- 0.2; P = 0.01; 1.2 +/- 0.1; P = 0.001, respectively); there was limited improvement in RBC-df in DPs treated with EPO and placebo. We conclude that EPO treatment significantly improved RBC-df in diabetic P-DPs, but EPO alone has no significant effect on RBC-df after 12 months in diabetic DPs. The combination of EPO and AG restores RBC-df to near-normal levels in diabetic DPs. We speculate that the effect of EPO on RBC-df seen in P-DPs and DPs is related to increased synthesis and influx of new and younger RBCs. AG may confer protection of RBCs in DPs by blocking advanced glycosylated end-product (AGE) formation. FAU - Brown, C D AU - Brown CD AD - Renal Diseases Division, Department of Medicine, State University of New York Downstate Medical Center, Brooklyn, NY 11203, USA. crownbrown@aol.com FAU - Zhao, Z H AU - Zhao ZH FAU - Thomas, L L AU - Thomas LL FAU - deGroof, R AU - deGroof R FAU - Friedman, E A AU - Friedman EA LA - eng PT - Clinical Trial PT - Comparative Study PT - Journal Article PT - Randomized Controlled Trial PL - United States TA - Am J Kidney Dis JT - American journal of kidney diseases : the official journal of the National Kidney Foundation JID - 8110075 RN - 0 (Guanidines) RN - 11096-26-7 (Erythropoietin) RN - SCQ4EZQ113 (pimagedine) SB - IM MH - Area Under Curve MH - Diabetic Nephropathies/blood/*therapy MH - Drug Therapy, Combination MH - Erythrocyte Deformability/*drug effects MH - Erythropoietin/*administration & dosage MH - Female MH - Guanidines/*administration & dosage MH - Hematocrit MH - Humans MH - Injections, Subcutaneous MH - Male MH - Middle Aged MH - Renal Dialysis MH - Uremia/blood/*therapy EDAT- 2001/12/01 10:00 MHDA- 2002/01/05 10:01 CRDT- 2001/12/01 10:00 PHST- 2001/12/01 10:00 [pubmed] PHST- 2002/01/05 10:01 [medline] PHST- 2001/12/01 10:00 [entrez] AID - S0272-6386(01)85044-7 [pii] AID - 10.1053/ajkd.2001.29281 [doi] PST - ppublish SO - Am J Kidney Dis. 2001 Dec;38(6):1414-20. doi: 10.1053/ajkd.2001.29281.