Literature DB >> 27094239

Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies.

Amit D Joshi1, Charlotte Andersson2, Stephan Buch3, Stefan Stender4, Raymond Noordam5, Lu-Chen Weng6, Peter E Weeke7, Paul L Auer8, Bernhard Boehm9, Constance Chen10, Hyon Choi11, Gary Curhan12, Joshua C Denny13, Immaculata De Vivo14, John D Eicher15, David Ellinghaus16, Aaron R Folsom6, Charles Fuchs17, Manish Gala18, Jeffrey Haessler19, Albert Hofman20, Frank Hu21, David J Hunter22, Harry L A Janssen23, Jae H Kang24, Charles Kooperberg19, Peter Kraft22, Wolfgang Kratzer9, Wolfgang Lieb25, Pamela L Lutsey6, Sarwa Darwish Murad26, Børge G Nordestgaard27, Louis R Pasquale28, Alex P Reiner19, Paul M Ridker29, Eric Rimm30, Lynda M Rose29, Christian M Shaffer31, Clemens Schafmayer32, Rulla M Tamimi33, André G Uitterlinden5, Uwe Völker34, Henry Völzke35, Yoshiyuki Wakabayashi36, Janey L Wiggs37, Jun Zhu36, Dan M Roden31, Bruno H Stricker5, Weihong Tang6, Alexander Teumer38, Jochen Hampe3, Anne Tybjærg-Hansen39, Daniel I Chasman29, Andrew T Chan40, Andrew D Johnson41.   

Abstract

BACKGROUND & AIMS: A genome-wide association study (GWAS) of 280 cases identified the hepatic cholesterol transporter ABCG8 as a locus associated with risk for gallstone disease, but findings have not been reported from any other GWAS of this phenotype. We performed a large-scale, meta-analysis of GWASs of individuals of European ancestry with available prior genotype data, to identify additional genetic risk factors for gallstone disease.
METHODS: We obtained per-allele odds ratio (OR) and standard error estimates using age- and sex-adjusted logistic regression models within each of the 10 discovery studies (8720 cases and 55,152 controls). We performed an inverse variance weighted, fixed-effects meta-analysis of study-specific estimates to identify single-nucleotide polymorphisms that were associated independently with gallstone disease. Associations were replicated in 6489 cases and 62,797 controls.
RESULTS: We observed independent associations for 2 single-nucleotide polymorphisms at the ABCG8 locus: rs11887534 (OR, 1.69; 95% confidence interval [CI], 1.54-1.86; P = 2.44 × 10(-60)) and rs4245791 (OR, 1.27; P = 1.90 × 10(-34)). We also identified and/or replicated associations for rs9843304 in TM4SF4 (OR, 1.12; 95% CI, 1.08-1.16; P = 6.09 × 10(-11)), rs2547231 in SULT2A1 (encodes a sulfoconjugation enzyme that acts on hydroxysteroids and cholesterol-derived sterol bile acids) (OR, 1.17; 95% CI, 1.12-1.21; P = 2.24 × 10(-10)), rs1260326 in glucokinase regulatory protein (OR, 1.12; 95% CI, 1.07-1.17; P = 2.55 × 10(-10)), and rs6471717 near CYP7A1 (encodes an enzyme that catalyzes conversion of cholesterol to primary bile acids) (OR, 1.11; 95% CI, 1.08-1.15; P = 8.84 × 10(-9)). Among individuals of African American and Hispanic American ancestry, rs11887534 and rs4245791 were associated positively with gallstone disease risk, whereas the association for the rs1260326 variant was inverse.
CONCLUSIONS: In this large-scale GWAS of gallstone disease, we identified 4 loci in genes that have putative functions in cholesterol metabolism and transport, and sulfonylation of bile acids or hydroxysteroids.
Copyright © 2016 AGA Institute. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  GWAS; Genetics; Risk Factors; SNP

Mesh:

Substances:

Year:  2016        PMID: 27094239      PMCID: PMC4959966          DOI: 10.1053/j.gastro.2016.04.007

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


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