4.6 Article

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

Journal

PLOS GENETICS
Volume 16, Issue 4, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1008629

Keywords

-

Funding

  1. National Institutes of Health [R01 HL127564]
  2. British Heart Foundation (British Heart Foundation Family Heart Study) [RG2000010]
  3. British Heart Foundation (UK Aneurysm Growth Study) [CS/14/2/30841]
  4. National Institute for Health Research (NIHR Leicester Cardiovascular Biomedical Research Unit Biomedical Research Informatics Centre for Cardiovascular Science) [IS_BRU_0211_20033]
  5. British Heart Foundation
  6. German Federal Ministry of Education and Research (BMBF)
  7. FP7 European Union project CVgenes@target [261123]
  8. Fondation Leducq (CADgenomics: Understanding Coronary Artery Disease Genes) [12CVD02]
  9. Deutsche Forschungsgemeinschaft cluster of excellence Inflammation at Interfaces
  10. Deutsche Forschungsgemeinschaft [SFB 1123]
  11. Programma di ricerca Regione-Universita? 2010-2012 Area 1-Strategic Programmes-Regione EmiliaRomagna
  12. National Heart, Lung, and Blood Institute [HHSN268201300046C, HHSN268201300047C, HHSN268201300048C, HHSN268201300049C, HHSN268201300050C]
  13. National Institute on Minority Health and Health Disparities [HHSN268201300046C, HHSN268201300047C, HHSN268201300048C, HHSN268201300049C, HHSN268201300050C]
  14. National Institute of General Medical Sciences [U54GM115428]
  15. National Human Genome Research Institute [1K08HG010155, 5UM1HG008895]
  16. UK Biobank [7089]
  17. Broad Institute of MIT and Harvard (BroadIgnite)
  18. Massachusetts General Hospital
  19. [RFPS-2007-3-644382]
  20. [RC2 HL103010]
  21. [RC2 HL102923]
  22. [RC2 HL102924]
  23. [5U54HG003067]

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Author summary Cirrhosis is a leading cause of death worldwide. However, the genetic underpinnings of cirrhosis remain poorly understood. In this study, we analyze twelve thousand individuals with cirrhosis and identify a common missense variant in a gene called MARC1 that protects against cirrhosis. Carriers of this missense variant also have lower blood cholesterol levels, lower liver enzyme levels and reduced liver fat. We identify an additional two low-frequency coding variants in MARC1 that are also associated with lower cholesterol levels, lower liver enzyme levels and protection from cirrhosis. Finally, we identify an individual homozygous for a predicted loss-of-function variant in MARC1 who exhibits very low blood LDL cholesterol levels. These genetic findings suggest that MARC1 deficiency may lower blood cholesterol levels and protect against cirrhosis, pointing to MARC1 as a potential therapeutic target for liver disease. Analyzing 12,361 all-cause cirrhosis cases and 790,095 controls from eight cohorts, we identify a common missense variant in the Mitochondrial Amidoxime Reducing Component 1 gene (MARC1 p.A165T) that associates with protection from all-cause cirrhosis (OR 0.91, p = 2.3*10(-11)). This same variant also associates with lower levels of hepatic fat on computed tomographic imaging and lower odds of physician-diagnosed fatty liver as well as lower blood levels of alanine transaminase (-0.025 SD, 3.7*10(-43)), alkaline phosphatase (-0.025 SD, 1.2*10(-37)), total cholesterol (-0.030 SD, p = 1.9*10(-36)) and LDL cholesterol (-0.027 SD, p = 5.1*10(-30)) levels. We identified a series of additional MARC1 alleles (low-frequency missense p.M187K and rare protein-truncating p.R200Ter) that also associated with lower cholesterol levels, liver enzyme levels and reduced risk of cirrhosis (0 cirrhosis cases for 238 R200Ter carriers versus 17,046 cases of cirrhosis among 759,027 non-carriers, p = 0.04) suggesting that deficiency of the MARC1 enzyme may lower blood cholesterol levels and protect against cirrhosis.

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