Correlation of hepcidin level with insulin resistance and endocrine glands function in major thalassemia

Adv Clin Exp Med. 2015 Jan-Feb;24(1):69-78. doi: 10.17219/acem/38158.

Abstract

Background: Hepcidin is a master regulator of iron metabolism that inhibits the transport of iron out of enterocytes and macrophages. Thalassemia major (TM) is associated with some of the endocrine disorders. However, studies have yet to be conducted on the correlation of hepcidin with hormone levels and insulin resistance (IR) in patients with TM.

Objectives: In the present study, the correlation of hepcidin level with some endocrine and biochemical parameters was investigated to determine the factors that mainly affect hepcidin correlation in patients with thalassemia. These factors include hormones, iron status, and IR parameters.

Material and methods: Hepcidin and other measured biochemical parameters were compared between the TM patients (100) and healthy children (37).

Results: Serum thyroid-stimulating hormone (TSH) was positively correlated (p < 0.05) with hepcidin, iron, and ferritin. T4 hormone was correlated with ferritin only. Other hormones showed different correlation patterns with iron status parameters but were statistically insignificant (p > 0.05). The percentage of β-cell function was the only parameter among the IR parameters that showed a significant difference between thalassemic and control groups.

Conclusions: Thyroid and β-cells dysfunctions are common in TM patients with frequent blood transfusions. In addition, hepcidin and TSH levels can be predicted significantly using the most correlated factors with hepcidin. These factors, including ferritin, insulin and TSH were used to construct predicting equations: S. Hepcidin = 0.003*Ferritin + 3.02*TSH + 0.12*Insulin + 16.85 (± 7.78) and TSH = 0.0083 × Insulin + 0.0042 × Ferritin + 0.0937 × Hepcidin + 1.91 (± 1.373).

MeSH terms

  • Biomarkers / blood
  • Cell Count
  • Child
  • Child, Preschool
  • Female
  • Ferritins / blood
  • Ferritins / genetics
  • Gene Expression
  • Hepcidins / blood*
  • Hepcidins / genetics
  • Humans
  • Insulin / blood*
  • Insulin / genetics
  • Insulin Resistance*
  • Insulin-Secreting Cells / metabolism
  • Insulin-Secreting Cells / pathology
  • Iron / blood
  • Iron Overload / blood*
  • Iron Overload / etiology
  • Iron Overload / physiopathology
  • Male
  • Thyroid Gland / metabolism
  • Thyroid Gland / physiopathology
  • Thyrotropin / blood
  • Thyrotropin / genetics
  • Thyroxine / blood
  • Thyroxine / genetics
  • Transfusion Reaction
  • beta-Thalassemia / blood*
  • beta-Thalassemia / genetics
  • beta-Thalassemia / physiopathology
  • beta-Thalassemia / therapy

Substances

  • Biomarkers
  • Hepcidins
  • Insulin
  • Thyrotropin
  • Ferritins
  • Iron
  • Thyroxine