Sequence variant at 4q25 near PITX2 associates with appendicitis

Sci Rep. 2017 Jun 8;7(1):3119. doi: 10.1038/s41598-017-03353-0.

Abstract

Appendicitis is one of the most common conditions requiring acute surgery and can pose a threat to the lives of affected individuals. We performed a genome-wide association study of appendicitis in 7,276 Icelandic and 1,139 Dutch cases and large groups of controls. In a combined analysis of the Icelandic and Dutch data, we detected a single signal represented by an intergenic variant rs2129979 [G] close to the gene PITX2 associating with increased risk of appendicitis (OR = 1.15, P = 1.8 × 10-11). We only observe the association in patients diagnosed in adulthood. The marker is close to, but distinct from, a set of markers reported to associate with atrial fibrillation, which have been linked to PITX2. PITX2 has been implicated in determination of right-left symmetry during development. Anomalies in organ arrangement have been linked to increased prevalence of gastrointestinal and intra-abdominal complications, which may explain the effect of rs2129979 on appendicitis risk.

MeSH terms

  • Alleles
  • Appendicitis / genetics*
  • Chromosomes, Human, Pair 4*
  • Computational Biology / methods
  • Genetic Predisposition to Disease*
  • Genetic Variation*
  • Genome-Wide Association Study*
  • Genotype
  • Homeobox Protein PITX2
  • Homeodomain Proteins / genetics*
  • Humans
  • Molecular Sequence Annotation
  • Odds Ratio
  • Transcription Factors / genetics*

Substances

  • Homeodomain Proteins
  • Transcription Factors