Relationship between erythropoietin responsiveness, insulin resistance, and malnutrition-inflammation-atherosclerosis (MIA) syndrome in hemodialysis patients with diabetes

Int J Artif Organs. 2011 Jan;34(1):16-25. doi: 10.5301/ijao.2011.6314.

Abstract

Background: This study aimed to explore the relationship between recombinant human erythropoietin (EPO) responsiveness, insulin resistance, and malnutrition-inflammation-atherosclerosis (MIA) syndrome in hemodialysis patients.

Methods: This was an observational cohort study in hemodialysis patients. Adipokines, inflammatory cytokines, and required EPO dosage were measured in diabetes (DM; n=58) and non-diabetes (non-DM; n=58) groups over 48 weeks. Furthermore, the EPO responsiveness index (required EPO dosage divided by hemoglobin) was evaluated with or without MIA syndrome in both groups.

Results: The DM group had significantly higher plasma leptin, interleukin-6 (IL-6), and high sensitivity C-reactive protein (hs-CRP) levels but lower plasma high molecular weight (HMW) adiponectin levels compared to the non-DM group. Although hemoglobin levels were not significantly different, required EPO dosage was significantly higher in the DM group than in the non-DM group, particularly in the presence of MIA syndrome. The DM group with MIA syndrome had significantly higher plasma leptin, IL-6, and hs-CRP levels but lower plasma HMW adiponectin levels compared to the non-DM group with MIA syndrome. There was also a significant association between EPO dosage and homeostasis model assessment for insulin resistance (HOMA-IR), hs-CRP, IL-6, tumor necrosis factor a, leptin, and HMW adiponectin levels in DM patients with MIA syndrome.

Conclusion: Diabetic hemodialysis patients with MIA syndrome have a lower response to EPO and a higher resistance to insulin. This fact may explain the poor outcome of these patients and demonstrate the importance of diagnosis and therapeutic management.

MeSH terms

  • Aged
  • Analysis of Variance
  • Anemia / blood
  • Anemia / drug therapy*
  • Anemia / etiology
  • Atherosclerosis / blood
  • Atherosclerosis / etiology*
  • Atherosclerosis / physiopathology
  • Biomarkers / blood
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / complications*
  • Diabetes Mellitus, Type 2 / physiopathology
  • Erythropoietin / therapeutic use*
  • Female
  • Glycated Hemoglobin / metabolism
  • Hematinics / therapeutic use*
  • Humans
  • Inflammation / blood
  • Inflammation / etiology*
  • Inflammation / physiopathology
  • Inflammation Mediators / blood
  • Insulin Resistance*
  • Japan
  • Kidney Failure, Chronic / blood
  • Kidney Failure, Chronic / complications
  • Kidney Failure, Chronic / physiopathology
  • Kidney Failure, Chronic / therapy*
  • Lipids / blood
  • Male
  • Malnutrition / blood
  • Malnutrition / etiology*
  • Malnutrition / physiopathology
  • Middle Aged
  • Prospective Studies
  • Recombinant Proteins
  • Renal Dialysis / adverse effects*
  • Syndrome
  • Time Factors
  • Treatment Outcome

Substances

  • Biomarkers
  • Blood Glucose
  • Glycated Hemoglobin A
  • Hematinics
  • Inflammation Mediators
  • Lipids
  • Recombinant Proteins
  • hemoglobin A1c protein, human
  • Erythropoietin