The Genetics of Primary Biliary Cholangitis: A GWAS and Post-GWAS Update

Primary biliary cholangitis (PBC) is a chronic, progressive cholestatic liver disease in which the small intrahepatic bile ducts are destroyed by autoimmune reactions. Among autoimmune diseases, which are polygenic complex traits caused by the combined contribution of genetic and environmental factors, PBC exhibits the strongest involvement of genetic heritability in disease development. As at December 2022, genome-wide association studies (GWASs) and associated meta-analyses identified approximately 70 PBC susceptibility gene loci in various populations, including those of European and East Asian descent. However, the molecular mechanisms through which these susceptibility loci affect the pathogenesis of PBC are not fully understood. This study provides an overview of current data regarding the genetic factors of PBC as well as post-GWAS approaches to identifying primary functional variants and effector genes in disease-susceptibility loci. Possible mechanisms of these genetic factors in the development of PBC are also discussed, focusing on four major disease pathways identified by in silico gene set analyses, namely, (1) antigen presentation by human leukocyte antigens, (2) interleukin-12-related pathways, (3) cellular responses to tumor necrosis factor, and (4) B cell activation, maturation, and differentiation pathways.

Automated summary

Primary biliary cholangitis (PBC) is a chronic liver disease caused by autoimmune reactions leading to the destruction of small intrahepatic bile ducts. Genetic factors play a significant role in the development of PBC, with approximately 70 susceptibility gene loci identified through genome-wide association studies. However, the specific molecular mechanisms underlying these susceptibility loci and their impact on PBC pathogenesis remain unclear. This study provides an overview of current research on the genetic factors of PBC and discusses potential mechanisms, focusing on four major disease pathways identified through gene set analyses.