Effect of Interleukin and Hepcidin in Anemia of Chronic Diseases

Maha F Yacoub1, Hala Fouad Ferwiz2, Fadwa Said3

  • 1Internal Medicine and Clinical Hematology, Faculty of Medicine, Cairo University, Giza, Egypt.

Anemia
|February 26, 2020
PubMed

Insights

Anemia of chronic disease (ACD) is linked to inflammation. This study found higher levels of interleukin-6 (IL-6) and hepcidin in ACD patients, suggesting their role in the condition.

Area of Science:

  • Hematology
  • Immunology
  • Pathophysiology

Background:

  • Anemia of chronic disease (ACD), also known as anemia of inflammation, is prevalent in elderly individuals with chronic conditions.
  • Interleukin-6 (IL-6), a pro-inflammatory cytokine, and hepcidin, an antimicrobial peptide, are implicated in ACD pathogenesis.
  • ACD is associated with chronic inflammation, infections, and cancers.

Purpose of the Study:

  • To investigate the role of interleukin-6 (IL-6) and hepcidin in the pathogenesis of anemia of chronic disease (ACD).
  • To compare red cell indices, iron profile, IL-6, and hepcidin levels between patients with ACD and healthy controls.

Main Methods:

  • The study included 40 patients with chronic diseases and 40 age-matched healthy controls.
  • Red cell indices, iron profile, serum IL-6, and hepcidin levels were measured.
  • Assays used included Bayer ADVIA 120, VITROS 5600, and ELISA.

Main Results:

  • Patients with ACD exhibited significantly lower hemoglobin, red blood cell count, hematocrit, serum iron, and MCHC compared to controls.
  • Serum total iron-binding capacity (TIBC) was also significantly lower in ACD patients.
  • Serum levels of both IL-6 and hepcidin were substantially higher in ACD patients than in controls (p < 0.001).

Conclusions:

  • A significant increase in serum IL-6 and hepcidin levels was observed in patients with ACD.
  • These findings highlight the crucial role of IL-6 and hepcidin in ACD pathogenesis.
  • The results provide a basis for developing novel therapeutic strategies targeting IL-6 and hepcidin to manage iron metabolism in ACD.
Abstract

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