Iron deficiency and frequency of HFE C282Y gene mutation in Brazilian blood donors

Abstract

Limited data are available about iron deficiency (ID) in Brazilian blood donors. This study evaluated the frequencies of ID and iron-deficiency anaemia (IDA) separately and according to frequency of blood donations. The protective effect of the heterozygous genotype for HFE C282Y mutation against ID and IDA in female blood donors was also determined. Five hundred and eight blood donors were recruited at the Blood Bank of Santa Casa in Sao Paulo, Brazil. Haemoglobin and serum ferritin concentrations were measured. The genotype for HFE C282Y mutation was determined by polymerase chain reaction followed by restriction fragment length polymorphism analysis. The ID was found in 21·1% of the women and 2·6% of the men whereas the IDA was found in 6·8 and 0·3%, respectively. The ID was found in 11·9% of the women in group 1 (first-time blood donors) and the frequency increased to 38·9% in women of the group 3 (blood donors donating once or more times in the last 12 months). No ID was found in men from group 1; however the ID frequency increased to 0·9% in group 2 (who had donated blood before but not in the last 12 months) and 5·0% in group 3. In summary, the heterozygous genotype was not associated with reduction of ID or IDA frequencies in both genders, but in male blood donors it was associated with a trend to elevated ferritin levels (P = 0·060). ID is most frequent in Brazilian women but was also found in men of group 3. © 2009 British Blood Transfusion Society.