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全基因组荟萃分析产生 46 个新的与铁稳态生物标志物相关的位点。

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

机构信息

The National Institute for Health Research Blood and Transplant Research Unit in Donor Health and Genomics at the University of Cambridge, University of Cambridge, Cambridge, UK.

British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.

出版信息

Commun Biol. 2021 Feb 3;4(1):156. doi: 10.1038/s42003-020-01575-z.

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.

摘要

铁对于许多生物学功能都是必不可少的,铁缺乏和铁过载对健康有重大影响。我们对来自冰岛、英国和丹麦的三项全基因组关联研究进行了荟萃分析,这些研究的对象是铁蛋白水平(N=246139)、总铁结合能力(N=135430)、铁(N=163511)和转铁蛋白饱和度(N=131471)。我们在 56 个基因座中发现了 62 个与铁稳态参数相关的独立序列变异,包括 46 个新基因座。DUOX2、F5、SLC11A2 和 TMPRSS6 中的变异与缺铁性贫血相关,而 TF、HFE、TFR2 和 TMPRSS6 中的变异与铁过载相关。HBS1L-MYB 基因间区域的变异与铁过载风险增加和缺铁性贫血风险降低均相关。该 DUOX2 错义变异在人群中存在于 14%,与所有铁稳态生物标志物相关,使缺铁性贫血的风险增加 29%。这些关联表明,这些变异所涉及的蛋白质参与了铁稳态的主要生理过程:铁感应和储存、炎症、肠道铁吸收、铁循环利用、红细胞生成和出血/月经。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3689/7859200/4b5fd957624f/42003_2020_1575_Fig1_HTML.jpg

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