| Literature DB >> 24405709 |
Vincent Zimmer1, Frank Lammert2.
Abstract
By implementation of novel genotyping technologies, progress in delineating the genetic architecture of acquired liver diseases has been achieved in recent years. The rapid dissemination of genome-wide linkage and association studies has paved the way for the identification of genetic variants that cause or modify non-viral liver diseases as well as the natural and treatment-related outcomes in chronic viral hepatitis. Invaluable genomic data has recently been derived from additional genome-wide association studies (GWAS) of the archetypical cholestatic liver diseases primary sclerosing cholangitis (PSC) and primary biliary cirrhosis (PBC). Beyond providing novel pathobiological insights in need of more sophisticated functional annotation, gene variation might in the future be instrumental in precise risk stratification and the development of genotype-based treatment algorithms. In this regard, the definition of subtypes of acquired liver disease and re-categorization of clinically defined disease phenotypes into a more 'genometype'-based disease classification represents a priority future research direction.Entities:
Keywords: ABC transporter; Cholelithiasis; Cholestasis; Epistasis; Genome-wide association studies
Mesh:
Year: 2013 PMID: 24405709 DOI: 10.1016/j.mam.2013.10.004
Source DB: PubMed Journal: Mol Aspects Med ISSN: 0098-2997