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Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration

Wilman, Henry R. ; Atabaki Pasdar, Naeimeh LU orcid ; Franks, Paul LU ; Giordano, Giuseppe LU ; Pomares-Millan, Hugo LU orcid ; Fitipaldi, Hugo LU ; Mutie, Pascal LU ; Klintenberg, Maria LU and Yaghootkar, Hanieh (2019) In Journal of Hepatology 71(3). p.594-602
Abstract
Background & Aims: Excess liver iron content is common and is linked to the risk of hepatic and extrahepatic diseases. We aimed to identify genetic variants influencing liver iron content and use genetics to understand its link to other traits and diseases. Methods: First, we performed a genome-wide association study (GWAS) in 8,289 individuals from UK Biobank, whose liver iron level had been quantified by magnetic resonance imaging, before validating our findings in an independent cohort (n = 1,513 from IMI DIRECT). Second, we used Mendelian randomisation to test the causal effects of 25 predominantly metabolic traits on liver iron content. Third, we tested phenome-wide associations between liver iron variants and 770 traits and... (More)
Background & Aims: Excess liver iron content is common and is linked to the risk of hepatic and extrahepatic diseases. We aimed to identify genetic variants influencing liver iron content and use genetics to understand its link to other traits and diseases. Methods: First, we performed a genome-wide association study (GWAS) in 8,289 individuals from UK Biobank, whose liver iron level had been quantified by magnetic resonance imaging, before validating our findings in an independent cohort (n = 1,513 from IMI DIRECT). Second, we used Mendelian randomisation to test the causal effects of 25 predominantly metabolic traits on liver iron content. Third, we tested phenome-wide associations between liver iron variants and 770 traits and disease outcomes. Results: We identified 3 independent genetic variants (rs1800562 [C282Y] and rs1799945 [H63D] in HFE and rs855791 [V736A] in TMPRSS6) associated with liver iron content that reached the GWAS significance threshold (p <5 × 10−8). The 2 HFE variants account for ∼85% of all cases of hereditary haemochromatosis. Mendelian randomisation analysis provided evidence that higher central obesity plays a causal role in increased liver iron content. Phenome-wide association analysis demonstrated shared aetiopathogenic mechanisms for elevated liver iron, high blood pressure, cirrhosis, malignancies, neuropsychiatric and rheumatological conditions, while also highlighting inverse associations with anaemias, lipidaemias and ischaemic heart disease. Conclusion: Our study provides genetic evidence that mechanisms underlying higher liver iron content are likely systemic rather than organ specific, that higher central obesity is causally associated with higher liver iron, and that liver iron shares common aetiology with multiple metabolic and non-metabolic diseases. Lay summary: Excess liver iron content is common and is associated with liver diseases and metabolic diseases including diabetes, high blood pressure, and heart disease. We identified 3 genetic variants that are linked to an increased risk of developing higher liver iron content. We show that the same genetic variants are linked to higher risk of many diseases, but they may also be associated with some health advantages. Finally, we use genetic variants associated with waist-to-hip ratio as a tool to show that central obesity is causally associated with increased liver iron content. © 2019 European Association for the Study of the Liver (Less)
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author collaboration
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Genetics, Genome-wide association study, Iron, Magnetic resonance imaging, Metabolic syndrome, Metabolism
in
Journal of Hepatology
volume
71
issue
3
pages
594 - 602
publisher
Elsevier
external identifiers
  • scopus:85068854139
  • pmid:31226389
ISSN
0168-8278
DOI
10.1016/j.jhep.2019.05.032
language
English
LU publication?
yes
additional info
Export Date: 25 July 2019
id
61d10647-2504-43f7-91ab-9010f171cb62
alternative location
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85068854139&doi=10.1016%2fj.jhep.2019.05.032&partnerID=40&md5=6a589d89b2a35b38fccec18c2c5c6c4b
date added to LUP
2019-07-25 09:40:25
date last changed
2024-05-28 21:21:49
@article{61d10647-2504-43f7-91ab-9010f171cb62,
  abstract     = {{Background &amp; Aims: Excess liver iron content is common and is linked to the risk of hepatic and extrahepatic diseases. We aimed to identify genetic variants influencing liver iron content and use genetics to understand its link to other traits and diseases. Methods: First, we performed a genome-wide association study (GWAS) in 8,289 individuals from UK Biobank, whose liver iron level had been quantified by magnetic resonance imaging, before validating our findings in an independent cohort (n = 1,513 from IMI DIRECT). Second, we used Mendelian randomisation to test the causal effects of 25 predominantly metabolic traits on liver iron content. Third, we tested phenome-wide associations between liver iron variants and 770 traits and disease outcomes. Results: We identified 3 independent genetic variants (rs1800562 [C282Y] and rs1799945 [H63D] in HFE and rs855791 [V736A] in TMPRSS6) associated with liver iron content that reached the GWAS significance threshold (p &lt;5 × 10−8). The 2 HFE variants account for ∼85% of all cases of hereditary haemochromatosis. Mendelian randomisation analysis provided evidence that higher central obesity plays a causal role in increased liver iron content. Phenome-wide association analysis demonstrated shared aetiopathogenic mechanisms for elevated liver iron, high blood pressure, cirrhosis, malignancies, neuropsychiatric and rheumatological conditions, while also highlighting inverse associations with anaemias, lipidaemias and ischaemic heart disease. Conclusion: Our study provides genetic evidence that mechanisms underlying higher liver iron content are likely systemic rather than organ specific, that higher central obesity is causally associated with higher liver iron, and that liver iron shares common aetiology with multiple metabolic and non-metabolic diseases. Lay summary: Excess liver iron content is common and is associated with liver diseases and metabolic diseases including diabetes, high blood pressure, and heart disease. We identified 3 genetic variants that are linked to an increased risk of developing higher liver iron content. We show that the same genetic variants are linked to higher risk of many diseases, but they may also be associated with some health advantages. Finally, we use genetic variants associated with waist-to-hip ratio as a tool to show that central obesity is causally associated with increased liver iron content. © 2019 European Association for the Study of the Liver}},
  author       = {{Wilman, Henry R. and Atabaki Pasdar, Naeimeh and Franks, Paul and Giordano, Giuseppe and Pomares-Millan, Hugo and Fitipaldi, Hugo and Mutie, Pascal and Klintenberg, Maria and Yaghootkar, Hanieh}},
  issn         = {{0168-8278}},
  keywords     = {{Genetics; Genome-wide association study; Iron; Magnetic resonance imaging; Metabolic syndrome; Metabolism}},
  language     = {{eng}},
  month        = {{06}},
  number       = {{3}},
  pages        = {{594--602}},
  publisher    = {{Elsevier}},
  series       = {{Journal of Hepatology}},
  title        = {{Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration}},
  url          = {{http://dx.doi.org/10.1016/j.jhep.2019.05.032}},
  doi          = {{10.1016/j.jhep.2019.05.032}},
  volume       = {{71}},
  year         = {{2019}},
}