PMID- 18045859 OWN - NLM STAT- MEDLINE DCOM- 20080130 LR - 20211020 IS - 1555-905X (Electronic) IS - 1555-9041 (Print) IS - 1555-9041 (Linking) VI - 3 IP - 1 DP - 2008 Jan TI - Serum albumin is strongly associated with erythropoietin sensitivity in hemodialysis patients. PG - 98-104 AB - BACKGROUND AND OBJECTIVES: In hemodialysis patients, the hematological response to erythropoietin (epo) is variable and clinical factors that explain this variability are incompletely understood. We tested the hypothesis that the variability in hemoglobin (Hgb) response (epo sensitivity) is determined by key nutritional, inflammation, and oxidative stress markers. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Eighty-two consecutive patients on hemodialysis had 3 consecutive monthly predialysis evaluations of Hgb, total white blood cell (WBC) count, serum albumin, malondialdehyde (MDA), and monocyte chemoattractant protein-1 (MCP1). We analyzed the time course of Hgb in relationship to serum albumin, WBC, MDA, MCP1, epo and iron administration, and tests of iron sufficiency in a linear growth curve model. RESULTS: Subjects with higher Hgb had a fall in Hgb and vice versa, regressing to a mean Hgb (SD) of 11.8 g/dl (1.8 g/dl). Whereas the average slope of Hgb was flat, the SD of slopes was 0.63 g/dl, which explained 39% of the variance in Hgb. Nonuse of epo was associated with a mean Hgb change of -0.18 g/dl (95% confidence interval [CI] -0.26 to -0.10) per 10,000 IU epo/mo (P < 0.05). Epo use was associated with steeper rate of change at 0.04 g/dl per mo per 10,000 IU (95% CI 0.01 to 0.07) (P < 0.01). Hgb at baseline was 0.73 g/dl higher for each 1-g/dl increase in albumin, and the rate of change increased by 0.49 g/dl per mo for each 1-g/dl increase in albumin concentration. WBC, MDA, or MCP1 had no role in predicting the baseline Hgb or its change over time. CONCLUSIONS: Serum albumin concentration is an important predictor of both baseline Hgb and epo sensitivity in chronic hemodialysis patients. Factors that improve serum albumin may also improve Hgb in hemodialysis patients. FAU - Agarwal, Rajiv AU - Agarwal R AD - Division of Nephrology, Department of Medicine, Indiana University School of Medicine, and the Richard L. RoudebushVA Medical Center, Indianapolis, Indiana 46202, USA. ragarwal@iupui.edu FAU - Davis, Joyce L AU - Davis JL FAU - Smith, Linda AU - Smith L LA - eng PT - Clinical Trial PT - Journal Article DEP - 20071128 PL - United States TA - Clin J Am Soc Nephrol JT - Clinical journal of the American Society of Nephrology : CJASN JID - 101271570 RN - 0 (Biomarkers) RN - 0 (CCL2 protein, human) RN - 0 (Chemokine CCL2) RN - 0 (Hemoglobins) RN - 0 (Serum Albumin) RN - 11096-26-7 (Erythropoietin) RN - 4Y8F71G49Q (Malondialdehyde) SB - IM MH - Adult MH - Aged MH - Anemia/blood/*drug therapy MH - Biomarkers MH - Chemokine CCL2/blood MH - Erythropoietin/*therapeutic use MH - Female MH - Hemoglobins/metabolism MH - Humans MH - Inflammation/blood MH - Kidney Failure, Chronic/blood/*complications MH - Leukocyte Count MH - Male MH - Malondialdehyde/blood MH - Middle Aged MH - Oxidative Stress MH - Predictive Value of Tests MH - Prospective Studies MH - *Renal Dialysis MH - Serum Albumin/*metabolism MH - Treatment Outcome PMC - PMC2390989 EDAT- 2007/11/30 09:00 MHDA- 2008/01/31 09:00 PMCR- 2009/01/01 CRDT- 2007/11/30 09:00 PHST- 2007/11/30 09:00 [pubmed] PHST- 2008/01/31 09:00 [medline] PHST- 2007/11/30 09:00 [entrez] PHST- 2009/01/01 00:00 [pmc-release] AID - CJN.03330807 [pii] AID - 0807 [pii] AID - 10.2215/CJN.03330807 [doi] PST - ppublish SO - Clin J Am Soc Nephrol. 2008 Jan;3(1):98-104. doi: 10.2215/CJN.03330807. Epub 2007 Nov 28.