Document Type: Research Paper
National Institute of Genetic Engineering and Biotechnology, P.O. Box 14965/161, Tehran, I.R. Iran.
Endocrine and Metabolism Research Center, Tehran University of Medical Sciences and Health Services, P.O. Box 14155-1771, Tehran, I.R. Iran.
Shaheed Rajaei Cardiovascular Medical and Research Center, P.O. Box 1996911151, Tehran, I.R. Iran.
Heme oxygenase-2 (HO-2) is a critical antioxidative stress enzyme found in endothelial cells and adventitial
nerves. This enzyme in conjunction with other HOs (1 and 3) metabolize heme molecule into ferrous iron,
carbon monoxide (CO), and biliverdin which is further converted to bilirubin. Both biliverdin and bilirubin are
potent antioxidants, reducing the risk of atherosclerosis. HO-2 also induces endothelial relaxation by synthesizing CO. This is the first study to evaluate the association of HO-2 gene mutation in patients affected
with atherosclerosis. Blood samples from patients (n=137) and normal controls (n=100) were collected.
Three pairs of primers were designed to amplify exons 2 to 4 related to human HO-2 gene. The PCR products
were analyzed by SSCP and sequencing to find out mutations. Iron and bilirubins (Total, Direct and
Indirect) levels were determined in patients and controls. Two nucleotide substitutions were found among
10% of patients, consisted of a newly reported transversion mutation, C to A substitution in codon A70D
(GCC to GAC) (Ala to Asp) and a previously reported transition mutation, A to G substitution in codon K89E
(AAG to GAG) (Leu to Glu). Significant associations were obtained between risk of atherosclerosis and
A437G substitution in codon K89E of HO-2 gene (P6.82) and reduced level of total (P6.01), and indirect (P< 0.016 and χ2>5.99) bilirubins with no significant association with serum iron and direct bilirubin. No significant associations were observed among C381A substitution incodon (A70D, P< 0.11 and χ2 >2.97), level of serum iron, bilirubin and risk of atherosclerosis. These findings indicate the importance of A437G substitution in the development of atherosclerosis. Further studies are required to study the association of HO-2 gene mutations with atherosclerosis in other populations.