Author:
Emdin Connor A.,Haas Mary,Khera Amit V.,Aragam Krishna,Chaffin Mark,Jiang Lan,Wei Wei-Qi,Feng Qiping,Karjalainen Juha,Havulinna Aki,Kiiskinen Tuomo,Bick Alexander,Ardissino Diego,Wilson James G.,Schunkert Heribert,McPherson Ruth,Watkins Hugh,Elosua Roberto,Bown Matthew J,Samani Nilesh J,Baber Usman,Erdmann Jeanette,Gupta Namrata,Danesh John,Saleheen Danish,Daly Mark,Denny Joshua,Gabriel Stacey,Kathiresan Sekar
Abstract
Analyzing 5770 all-cause cirrhosis cases and 572,850 controls from seven cohorts, we identify a missense variant in the Mitochondrial Amidoxime Reducing Component 1 gene (MARC1 p.A165T) that associates with protection from all-cause cirrhosis (OR 0.88, p=2.1*10−8). 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 (−0.012 SD, 1.4*10−8), alkaline phosphatase (−0.019 SD, 6.6*10−9), total cholesterol (−0.037 SD, p=1*10−18) and LDL cholesterol (−0.035 SD, p=7.3*10−16). Carriers of rare protein-truncating variants in MARC1 had lower liver enzyme levels, cholesterol levels, and reduced odds of liver disease (OR 0.19, p= 0.04) suggesting that deficiency of the MARC1 enzyme protects against cirrhosis.
Publisher
Cold Spring Harbor Laboratory
Cited by
5 articles.
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