Association of malnutrition-inflammation complex and responsiveness to erythropoiesis stimulating agents in hemodialysis patients

Protein-energy wasting, inflammation and refractory anemia are common in long-term hemodialysis patients. A decreased responsiveness to erythropoiesis stimulating agents (ESA) is often the cause of the refractory anemia. A 6-year prospective cohort study of 754 hemodialysis patients, we hypothesized...

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Main Authors: Manoch Rattanasompattikul (Author), Miklos Z Molnar (Author), Joshua J Zaritsky (Author), Parta Hatamizadeh (Author), Jennie Jing (Author), Keith C Norris (Author), Csaba P Kovesdy (Author), Kamyar Kalantar-Zadeh (Author)
Format: Book
Published: The Korean Society of Nephrology, 2012-06-01T00:00:00Z.
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Summary:Protein-energy wasting, inflammation and refractory anemia are common in long-term hemodialysis patients. A decreased responsiveness to erythropoiesis stimulating agents (ESA) is often the cause of the refractory anemia. A 6-year prospective cohort study of 754 hemodialysis patients, we hypothesized that malnutrition-inflammation score (MIS) is an independent predictor of decreased responsiveness to ESAs (ERI) in hemodialysis patients. Mean age of patients was 54±15 years, 53% were diabetic and 49% Hispanic. A positive correlation was found between ERI and inflammatory markers including C-reactive protein (CRP) (r=0.16) and interleukin-6 (IL-6) (r=0.16). We also found negative correlations between ERI and serum albumin (r=−0.22). Each 5 unit higher MIS, 1 mg/L higher CRP and 0.5 g/dl lower albumin were associated with 46%, 45% and 140% higher likelihood of highest vs. lowest ERI in fully adjusted logistic regression models (odds ratio [and 95% CI] of 1.46 [1.05-2.05], 1.45 [1.06-1.98], and 2.40 [1.54-3.74]) respectively. Cubic splines illustrated continuous and incremental nature of MIS and ERI associations (Figure). Malnutrition-inflammation complex is a significant and independent predictor of decreased responsiveness to ESAs in hemodialysis patients. fx1
Item Description:2211-9132
10.1016/j.krcp.2012.04.488