Genome-Wide Association Studies in Primary Biliary Cirrhosis

Aliya F. Gulamhusein, Brian D. Juran, Konstantinos N. Lazaridis

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

Genome-wide association studies (GWASs) have been a significant technological advance in our ability to evaluate the genetic architecture of complex diseases such as primary biliary cirrhosis (PBC). To date, six large-scale studies have been performed that have identified 27 risk loci in addition to human leukocyte antigen (HLA) associated with PBC. The identified risk variants emphasize important disease concepts; namely, that disturbances in immunoregulatory pathways are important in the pathogenesis of PBC and that such perturbations are shared among a diverse number of autoimmune diseases--suggesting the risk architecture may confer a generalized propensity to autoimmunity not necessarily specific to PBC. Furthermore, the impact of non-HLA risk variants, particularly in genes involved with interleukin-12 signaling, and ethnic variation in conferring susceptibility to PBC have been highlighted. Although GWASs have been a critical stepping stone in understanding common genetic variation contributing to PBC, limitations pertaining to power, sample availability, and strong linkage disequilibrium across genes have left us with an incomplete understanding of the genetic underpinnings of disease pathogenesis. Future efforts to gain insight into this missing heritability, the genetic variation that contributes to important disease outcomes, and the functional consequences of associated variants will be critical if practical clinical translation is to be realized.

Original languageEnglish (US)
Pages (from-to)392-401
Number of pages10
JournalSeminars in liver disease
Volume35
Issue number4
DOIs
StatePublished - Nov 1 2015

Keywords

  • autoimmunity
  • genetics
  • genome-wide association studies
  • primary biliary cirrhosis

ASJC Scopus subject areas

  • Hepatology

Fingerprint Dive into the research topics of 'Genome-Wide Association Studies in Primary Biliary Cirrhosis'. Together they form a unique fingerprint.

Cite this