Primary Biliary Cholangitis in British Columbia First Nations: Clinical features and discovery of novel genetic susceptibility loci

Liver Int. 2018 May;38(5):940-948. doi: 10.1111/liv.13686. Epub 2018 Jan 23.

Abstract

Background & aims: Primary Biliary Cholangitis (PBC) is a chronic autoimmune liver disease characterized by destruction of intrahepatic bile ducts, portal inflammation and cirrhosis. Although rare in most populations, it is prevalent and often familial in British Columbia First Nations. We hypothesized that major genetic factors increased the risk in First Nations.

Methods: In all, 44 individuals with Primary Biliary Cholangitis and 61 unaffected relatives from 32 First Nations families participated. Family history and co-morbidities were documented. Medical records were reviewed and available biopsies were re-reviewed by our team pathologist. Genotyping was performed on DNA from 36 affected persons and 27 unaffected relatives using the Affymetrix Human Mapping 500K Array Set. MERLIN software was used to carry out multipoint parametric and nonparametric linkage analysis. Candidate genes were identified and entered into InnateDB and KEGG software to identify potential pathways affecting pathogenesis.

Results: In all, 34% of families were multiplex. Fifty per cent of cases and 33% of unaffected relatives reported other autoimmune disease. Three genomic regions (9q21, 17p13 and 19p13) produced LOD scores of 2.3 or greater suggestive of linkage, but no single linkage peak reached statistical significance. Candidate genes identified in the three regions suggested involvement of IL17, NFκB, IL6, JAK-STAT, IFNγ and TGFβ immune signalling pathways. Specifically, four genes-ACT1, PIN1, DNMT1 and NTN1-emerged as having roles in these pathways that may influence Primary Biliary Cholangitis pathogenesis.

Conclusions: Our whole genome linkage study results reflect the multifactorial nature of Primary Biliary Cholangitis, support previous studies suggesting signalling pathway involvement and identify new candidate genes for consideration.

Keywords: First Nations; Indigenous; Primary Biliary Cholangitis; genetic linkage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Adult
  • Autoimmune Diseases / ethnology
  • Autoimmune Diseases / genetics
  • British Columbia / ethnology
  • Case-Control Studies
  • DNA (Cytosine-5-)-Methyltransferase 1 / genetics
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • Indians, North American / genetics*
  • Liver Cirrhosis, Biliary / ethnology*
  • Liver Cirrhosis, Biliary / genetics*
  • Lod Score
  • Male
  • Middle Aged
  • NIMA-Interacting Peptidylprolyl Isomerase / genetics
  • Netrin-1 / genetics
  • Tumor Necrosis Factor Receptor-Associated Peptides and Proteins / genetics

Substances

  • Adaptor Proteins, Signal Transducing
  • NIMA-Interacting Peptidylprolyl Isomerase
  • NTN1 protein, human
  • TRAF3IP2 protein, human
  • Tumor Necrosis Factor Receptor-Associated Peptides and Proteins
  • Netrin-1
  • DNA (Cytosine-5-)-Methyltransferase 1
  • DNMT1 protein, human
  • PIN1 protein, human