Four variants in transferrin and HFE genes as potential markers of iron deficiency anaemia risk: An association study in menstruating women

Background: Iron deficiency anaemia is a worldwide health problem in which environmental, physiologic and genetic factors play important roles. The associations between iron status biomarkers and single nucleotide polymorphisms (SNPs) known to be related to iron metabolism were studied in menstruati...

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Detalles Bibliográficos
Autores: Blanco-Rojo R., Baeza-Richer C., Lápez-Parra A.M., Pérez-Granados A.M., Brichs A., Bertoncini S., Buil A., Arroyo-Pardo E., Soria J.M., Vaquero M.P.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2011
País:España
Institución:Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
Repositorio:r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
OAI Identifier:oai:iibsantpau.fundanetsuite.com:p10553
Acceso en línea:https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10553
https://www.scopus.com/inward/record.uri?eid=2-s2.0-80053487857&doi=10.1186%2f1743-7075-8-69&partnerID=40&md5=0bffa488f3f687edae125883ecc6dcc8
Access Level:acceso abierto
Palabra clave:aspartic acid
cysteine
ferritin
hemoglobin
HFE protein
histidine
transferrin
tryptophan
adult
allele
article
Caucasian
female
ferritin blood level
gene mutation
genetic association
genetic variability
hematocrit
hemoglobin blood level
heterozygosity
high risk population
homozygosity
human
iron deficiency anemia
mean corpuscular volume
menstruation
single nucleotide polymorphism
transferrin blood level
Descripción
Sumario:Background: Iron deficiency anaemia is a worldwide health problem in which environmental, physiologic and genetic factors play important roles. The associations between iron status biomarkers and single nucleotide polymorphisms (SNPs) known to be related to iron metabolism were studied in menstruating women. Methods. A group of 270 Caucasian menstruating women, a population group at risk of iron deficiency anaemia, participated in the study. Haematological and biochemical parameters were analysed and 10 selected SNPs were genotyped by minisequencing assay. The associations between genetic and biochemical data were analysed by Bayesian Model Averaging (BMA) test and decision trees. Dietary intake of a representative subgroup of these volunteers (n = 141) was assessed, and the relationship between nutrients and iron biomarkers was also determined by linear regression. Results: Four variants, two in the transferrin gene (rs3811647, rs1799852) and two in the HFE gene (C282Y, H63D), explain 35% of the genetic variation or heritability of serum transferrin in menstruating women. The minor allele of rs3811647 was associated with higher serum transferrin levels and lower transferrin saturation, while the minor alleles of rs1799852 and the C282Y and H63D mutations of HFE were associated with lower serum transferrin levels. No association between nutrient intake and iron biomarkers was found. Conclusions: In contrast to dietary intake, these four SNPs are strongly associated with serum transferrin. Carriers of the minor allele of rs3811647 present a reduction in iron transport to tissues, which might indicate higher iron deficiency anaemia risk, although the simultaneous presence of the minor allele of rs1799852 and HFE mutations appear to have compensatory effects. Therefore, it is suggested that these genetic variants might potentially be used as markers of iron deficiency anaemia risk. © 2011 Blanco-Rojo et al; licensee BioMed Central Ltd.