Evidence for a proatherogenic biochemical phenotype in beta thalassemia minor and intermedia

Acta Haematol. 2011;126(2):87-94. doi: 10.1159/000327252. Epub 2011 May 11.

Abstract

The purpose of this study was to focus on pathophysiological mechanisms linking β-thalassemia intermedia (β-TI) and minor (β-TMI) with cardiovascular risk. Iron status, prooxidant-antioxidant balance and lipid profiles in serum, and lipid content in peripheral blood mononuclear cells (PBMCs) were evaluated in 20 β-TMI subjects, 22 β-TI patients and in 30 nonthalassemic blood donors. The mRNA levels of some genes involved in the regulation of iron and cholesterol metabolism were also determined. In β-TI and in β-TMI, serum iron, prooxidant-antioxidant ratio, transferrin saturation and erythropoietin levels were higher, while transferrin and hepcidin were lower compared to controls. Hepcidin and interleukin-1α mRNA levels were found to be reduced in β-TI- and β-TMI-PBMCs, while those of tumor necrosis factor alpha were increased. A reduction in high-density lipoprotein cholesterol in serum and an accumulation of neutral lipids coupled with increased mRNA levels of acetyl-coenzyme A:cholesterol acyltransferase and decreased neutral cholesterol ester hydrolase in PBMCs were also observed in β-TI and β-TMI compared to controls. Taken together, these findings provide experimental support for the idea that not only β-TI patients but also β-TMI have a proatherogenic biochemical phenotype which may contribute to increase their cardiovascular disease risk.

MeSH terms

  • Acetyl-CoA C-Acetyltransferase / genetics
  • Acetyl-CoA C-Acetyltransferase / metabolism
  • Adult
  • Antimicrobial Cationic Peptides / blood
  • Antimicrobial Cationic Peptides / genetics
  • Antimicrobial Cationic Peptides / metabolism
  • Atherosclerosis / epidemiology
  • Atherosclerosis / etiology*
  • Cholesterol, HDL / blood
  • Erythropoietin / blood
  • Female
  • Hepcidins
  • Humans
  • Interleukin-1alpha / genetics
  • Interleukin-1alpha / metabolism
  • Iron / analysis
  • Iron / blood
  • Italy / epidemiology
  • Leukocytes, Mononuclear / metabolism
  • Male
  • Middle Aged
  • Oxidative Stress
  • Phenotype
  • RNA, Messenger / metabolism
  • Risk Factors
  • Severity of Illness Index
  • Sterol Esterase / genetics
  • Sterol Esterase / metabolism
  • Transferrin / chemistry
  • Transferrin / metabolism
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism
  • beta-Thalassemia / blood
  • beta-Thalassemia / metabolism
  • beta-Thalassemia / physiopathology*

Substances

  • Antimicrobial Cationic Peptides
  • Cholesterol, HDL
  • EPO protein, human
  • HAMP protein, human
  • Hepcidins
  • IL1A protein, human
  • Interleukin-1alpha
  • RNA, Messenger
  • TNF protein, human
  • Transferrin
  • Tumor Necrosis Factor-alpha
  • Erythropoietin
  • Iron
  • ACAT1 protein, human
  • Acetyl-CoA C-Acetyltransferase
  • Sterol Esterase