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Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology.
- Source :
-
Nature communications [Nat Commun] 2021 Feb 05; Vol. 12 (1), pp. 816. Date of Electronic Publication: 2021 Feb 05. - Publication Year :
- 2021
-
Abstract
- Serum liver enzyme concentrations are the most frequently-used laboratory markers of liver disease, a major cause of mortality. We conduct a meta-analysis of genome-wide association studies of liver enzymes from UK BioBank and BioBank Japan. We identified 160 previously-unreported independent alanine aminotransferase, 190 aspartate aminotransferase, and 199 alkaline phosphatase genome-wide significant associations, with some affecting multiple different enzymes. Associated variants implicate genes that demonstrate diverse liver cell type expression and promote a range of metabolic and liver diseases. These findings provide insight into the pathophysiology of liver and other metabolic diseases that are associated with serum liver enzyme concentrations.
- Subjects :
- Alanine Transaminase blood
Alkaline Phosphatase blood
Aspartate Aminotransferases blood
Biological Specimen Banks
Endothelial Cells enzymology
Endothelial Cells pathology
Gene Expression Regulation
Genome-Wide Association Study
Hepatocytes enzymology
Hepatocytes pathology
Humans
Japan
Killer Cells, Natural enzymology
Killer Cells, Natural pathology
Kupffer Cells enzymology
Kupffer Cells pathology
Liver pathology
Liver Diseases blood
Liver Diseases classification
Liver Diseases pathology
Quantitative Trait Loci
Quantitative Trait, Heritable
Single-Cell Analysis
United Kingdom
Alanine Transaminase genetics
Alkaline Phosphatase genetics
Aspartate Aminotransferases genetics
Genome, Human
Liver enzymology
Liver Diseases genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 12
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 33547301
- Full Text :
- https://doi.org/10.1038/s41467-020-20870-1