The Study of HFE Genotypes and Its Expression Effect on Iron Status of Iranian Haemochromatosis, Iron Deficiency Anemia Patients, Iron-Taker and Non Iron-Taker Controls

Author(s): Elham Beiranvand, Saeid Abediankenari, Mosayeb Rostamian, Behnoush Beiranvand, Saeed Naazeri

Journal Name: Recent Advances in DNA & Gene Sequences (Discontinued)
Formerly Recent Patents on DNA & Gene Sequences

Volume 9 , Issue 1 , 2015

Graphical Abstract:


The role of HFE gene mutations or its expression in regulation of iron metabolism of hereditary haemochromatosis (HH) patients is remained controversial. Therefore here the correlation between two common HFE genotype (p.C282Y, p.H63D) and HFE gene expression with iron status in HH, iron deficiency anemia (IDA) and healthy Iranian participants was studied. For this purpose genotype determination was done by polymerase chain reaction - restriction fragment length polymorphism (PCR-RFLP). Real–Time PCR was applied for evaluation of HFE gene expression. Biochemical parameters and iron consumption were also assessed. Homozygote p.H63D mutation was seen in all HH patients and p.C282Y was not observed in any member of the population. A significant correlation was observed between serum ferritin (SF) level and gender or age of HH patients. p.H63D homozygote was seen to be able to significantly increase SF and transfer¬rin saturation (TS) level without affecting on liver function. Our results also showed that iron consumption affects on TS level increasing. HFE gene expression level of IDA patients was significantly higher than other groups. Also the HFE gene expression was negatively correlated with TS. Finally, the main result of our study showed that loss of HFE function in HH is not derived from its gene expression inhibition and much higher HFE gene expression might lead to IDA. However we propose repeating of the study for more approval of our finding.

Keywords: HFE gene, hereditary haemochromatosis, iron deficiency anemia, p.H63D mutation.

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Article Details

Year: 2015
Published on: 26 January, 2016
Page: [58 - 64]
Pages: 7
DOI: 10.2174/2352092209666150211233434

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