A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Stephan Buch - , Kiel University (Author)
  • Clemens Schafmayer - , Kiel University (Author)
  • Henry Völzke - , University of Greifswald (Author)
  • Christian Becker - , University of Cologne, RZPD German Resource Center for Genome Research (Author)
  • Andre Franke - , Kiel University (Author)
  • Huberta Von Eller-Eberstein - , Kiel University (Author)
  • Christian Kluck - , University of Cologne, RZPD German Resource Center for Genome Research (Author)
  • Ingelore Bässmann - , University of Cologne, RZPD German Resource Center for Genome Research (Author)
  • Mario Brosch - , Kiel University (Author)
  • Frank Lammert - , University of Bonn (Author)
  • Juan Francisco Miquel - , Pontificia Universidad Católica de Chile (Author)
  • Flavio Nervi - , Pontificia Universidad Católica de Chile (Author)
  • Michael Wittig - , Kiel University (Author)
  • Dieter Rosskopf - , University of Greifswald (Author)
  • Birgit Timm - , Kiel University (Author)
  • Christine Höll - , Kiel University (Author)
  • Marcus Seeger - , Kiel University (Author)
  • Abdou Elsharawy - , Kiel University (Author)
  • Tim Lu - , Kiel University (Author)
  • Jan Egberts - , Kiel University (Author)
  • Fred Fändrich - , Kiel University (Author)
  • Ulrich R. Fölsch - , Kiel University (Author)
  • Michael Krawczak - , Kiel University (Author)
  • Stefan Schreiber - , Kiel University (Author)
  • Peter Nürnberg - , University of Cologne (Author)
  • Jürgen Tepel - , Kiel University (Author)
  • Jochen Hampe - , Kiel University (Author)

Abstract

With an overall prevalence of 10-20%, gallstone disease (cholelithiasis) represents one of the most frequent and economically relevant health problems of industrialized countries. We performed an association scan of >500,000 SNPs in 280 individuals with gallstones and 360 controls. A follow-up study of the 235 most significant SNPs in 1,105 affected individuals and 873 controls replicated the disease association of SNP A-1791411 in ABCG8 (allelic P value PCCA = 4.1 × 10-9), which was subsequently attributed to coding variant rs11887534 (D19H). Additional replication was achieved in 728 German (P = 2.8 × 10-7) and 167 Chilean subjects (P = 0.02). The overall odds ratio for D19H carriership was 2.2 (95% confidence interval: 1.8-2.6, P = 1.4 × 10-14) in the full German sample. Association was stronger in subjects with cholesterol gallstones (odds ratio = 3.3), suggesting that His19 might be associated with a more efficient transport of cholesterol into the bile.

Details

Original languageEnglish
Pages (from-to)995-999
Number of pages5
JournalNature genetics
Volume39
Issue number8
Publication statusPublished - Aug 2007
Peer-reviewedYes
Externally publishedYes

External IDs

PubMed 17632509
ORCID /0000-0003-2928-015X/work/146166312

Keywords

Sustainable Development Goals

ASJC Scopus subject areas