Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

• Published in: Nature communications Vol. 5; no. 1; p. 4926
• Main Authors: Benyamin, Beben, Esko, Tonu, Ried, Janina S., Radhakrishnan, Aparna, Vermeulen, Sita H., Traglia, Michela, Gögele, Martin, Anderson, Denise, Broer, Linda, Podmore, Clara, Luan, Jian’an, Kutalik, Zoltan, Sanna, Serena, van der Meer, Peter, Tanaka, Toshiko, Wang, Fudi, Westra, Harm-Jan, Franke, Lude, Mihailov, Evelin, Milani, Lili, Hälldin, Jonas, Winkelmann, Juliane, Meitinger, Thomas, Thiery, Joachim, Peters, Annette, Waldenberger, Melanie, Rendon, Augusto, Jolley, Jennifer, Sambrook, Jennifer, Kiemeney, Lambertus A., Sweep, Fred C., Sala, Cinzia F., Schwienbacher, Christine, Pichler, Irene, Hui, Jennie, Demirkan, Ayse, Isaacs, Aaron, Amin, Najaf, Steri, Maristella, Waeber, Gérard, Verweij, Niek, Powell, Joseph E., Nyholt, Dale R., Heath, Andrew C., Madden, Pamela A. F., Visscher, Peter M., Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G., Hernandez, Dena, Bandinelli, Stefania, van der Harst, Pim, Uda, Manuela, Vollenweider, Peter, Scott, Robert A., Langenberg, Claudia, Wareham, Nicholas J., van Duijn, Cornelia, Beilby, John, Pramstaller, Peter P., Hicks, Andrew A., Ouwehand, Willem H., Oexle, Konrad, Gieger, Christian, Metspalu, Andres, Camaschella, Clara, Toniolo, Daniela, Swinkels, Dorine W., Whitfield, John B.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 29.10.2014; Nature Publishing Group
• Subjects: 692/420/2489/144; 692/699/317; Adult; Chromosomes, Human, Pair 7 - genetics; Ferritins - metabolism; Gene Expression Regulation; Genetic Association Studies; Genetic Loci; Genetic Predisposition to Disease; Hemochromatosis - blood; Hemochromatosis - genetics; Homeostasis - genetics; Humanities and Social Sciences; Humans; Iron - blood; Iron - metabolism; Lipids - blood; multidisciplinary; Phenotype; Polymorphism, Single Nucleotide - genetics; Reproducibility of Results; Risk Factors; Science; Science (multidisciplinary); Transferrin - metabolism
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/ncomms5926

Variation in body iron is associated with or causes diseases, including anaemia and iron overload. Here, we analyse genetic association data on biochemical markers of iron status from 11 European-population studies, with replication in eight additional cohorts (total up to 48,972 subjects). We find 11 genome-wide-significant ( P <5 × 10 −8 ) loci, some including known iron-related genes ( HFE, SLC40A1, TF, TFR2, TFRC, TMPRSS6 ) and others novel ( ABO, ARNTL , FADS2, NAT2 , TEX14 ). SNPs at ARNTL, TF , and TFR2 affect iron markers in HFE C282Y homozygotes at risk for hemochromatosis. There is substantial overlap between our iron loci and loci affecting erythrocyte and lipid phenotypes. These results will facilitate investigation of the roles of iron in disease. Iron deficiency is the leading cause of anaemia and is known to compromise immune function. Here, the authors identify several new genes associated with iron status in European populations and provide insight into how iron levels may be linked to the risk of metabolic disease.