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A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis

Abstract:
Iron is essential for many biological functions and iron deficiency and overload have major health implications. We performed a meta-analysis of three genome-wide association studies from Iceland, the UK and Denmark of blood levels of ferritin (N = 246,139), total iron binding capacity (N = 135,430), iron (N = 163,511) and transferrin saturation (N = 131,471). We found 62 independent sequence variants associating with iron homeostasis parameters at 56 loci, including 46 novel loci. Variants at DUOX2, F5, SLC11A2 and TMPRSS6 associate with iron deficiency anemia, while variants at TF, HFE, TFR2 and TMPRSS6 associate with iron overload. A HBS1L-MYB intergenic region variant associates both with increased risk of iron overload and reduced risk of iron deficiency anemia. The DUOX2 missense variant is present in 14% of the population, associates with all iron homeostasis biomarkers, and increases the risk of iron deficiency anemia by 29%. The associations implicate proteins contributing to the main physiological processes involved in iron homeostasis: iron sensing and storage, inflammation, absorption of iron from the gut, iron recycling, erythropoiesis and bleeding/menstruation.
Publication status:
Published
Peer review status:
Peer reviewed

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Authors


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Funder identifier:
10.13039/501100000274
Grant:
RG/18/13/33946
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Funder identifier:
10.13039/501100000272
Grant:
Senior Investigator Award
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Funder identifier:
10.13039/501100001923
Grant:
NIHR BTRU-2014-10024


Publisher:
Nature Research
Journal:
Communications Biology More from this journal
Volume:
4
Issue:
1
Pages:
156-156
Article number:
156
Publication date:
2021-02-03
DOI:
EISSN:
2399-3642
ISSN:
2399-3642


Language:
English
Keywords:
Pubs id:
1191270
Local pid:
pubs:1191270
Source identifiers:
W3127200818
Deposit date:
2026-03-25
ARK identifier:
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