Literature DB >> 23753274

Extreme bilirubin levels as a causal risk factor for symptomatic gallstone disease.

Stefan Stender1, Ruth Frikke-Schmidt, Børge G Nordestgaard, Anne Tybjærg-Hansen.   

Abstract

IMPORTANCE: In individuals without blockage of their bile ducts, levels of plasma bilirubin likely reflect levels of biliary bilirubin; higher biliary bilirubin levels may increase the risk of gallstone disease.
OBJECTIVE: To test the hypothesis that a lifelong increase in plasma bilirubin levels is a causal risk factor for symptomatic gallstone disease in the general population. DESIGN, SETTING, AND PARTICIPANTS: In a prospective study of the Danish general population (N = 61,212), we first tested whether elevated levels of plasma bilirubin predicted greater risk of symptomatic gallstone disease. Second, taking advantage of mendelian randomization, we tested whether a genetic variant in the bilirubin glucoronidating enzyme UGT1A1 (rs6742078) was associated with increased plasma bilirubin levels and, in turn, with an increased risk of symptomatic gallstone disease. MAIN OUTCOMES AND MEASURES: Plasma bilirubin level and symptomatic gallstone disease.
RESULTS: During 34 years of follow-up, 3374 individuals developed symptomatic gallstone disease. In adjusted analyses, persons with plasma bilirubin levels in the 10th decile had a greater risk of symptomatic gallstone disease compared with those with plasma bilirubin levels in deciles 1 through 9; the hazard ratios (HRs) (95% CIs) were 1.57 (1.26-1.96) overall, 1.36 (1.02-1.82) in women, and 2.00 (1.41-2.83) in men. UGT1A1 genotype explained 20% of the total variation in plasma bilirubin levels and was associated with increases in the mean plasma bilirubin level overall of +16% (+0.09 mg/dL) in GT heterozygotes and +90% (+0.50 mg/dL) in TT homozygotes compared with GG homozygotes, with similar effects in women and men (P for trend <.001 for all). The corresponding HRs (95% CIs) for symptomatic gallstone disease were 1.09 (1.02-1.17) for GT heterozygotes and 1.22 (1.09-1.36) for TT homozygotes vs GG homozygotes and similar in women and men (P for trend = .04-<.001). CONCLUSIONS AND RELEVANCE: These results are compatible with a causal association between extreme levels of plasma bilirubin and increased risk of symptomatic gallstone disease.

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Year:  2013        PMID: 23753274     DOI: 10.1001/jamainternmed.2013.6465

Source DB:  PubMed          Journal:  JAMA Intern Med        ISSN: 2168-6106            Impact factor:   21.873


  18 in total

1.  Gallbladder: High levels of bilirubin as a risk factor for symptomatic gallstone disease.

Authors:  Claire Greenhill
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2013-06-25       Impact factor: 46.802

2.  Safety and metabolic outcomes of resveratrol supplementation in older adults: results of a twelve-week, placebo-controlled pilot study.

Authors:  Stephen D Anton; Chelsea Embry; Michael Marsiske; Xiaomin Lu; Hani Doss; Christiaan Leeuwenburgh; Todd M Manini
Journal:  Exp Gerontol       Date:  2014-05-24       Impact factor: 4.032

3.  Evaluating elevated bilirubin levels in asymptomatic adults.

Authors:  Lisa B VanWagner; Richard M Green
Journal:  JAMA       Date:  2015-02-03       Impact factor: 56.272

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

Authors:  Amit D Joshi; Charlotte Andersson; Stephan Buch; Stefan Stender; Raymond Noordam; Lu-Chen Weng; Peter E Weeke; Paul L Auer; Bernhard Boehm; Constance Chen; Hyon Choi; Gary Curhan; Joshua C Denny; Immaculata De Vivo; John D Eicher; David Ellinghaus; Aaron R Folsom; Charles Fuchs; Manish Gala; Jeffrey Haessler; Albert Hofman; Frank Hu; David J Hunter; Harry L A Janssen; Jae H Kang; Charles Kooperberg; Peter Kraft; Wolfgang Kratzer; Wolfgang Lieb; Pamela L Lutsey; Sarwa Darwish Murad; Børge G Nordestgaard; Louis R Pasquale; Alex P Reiner; Paul M Ridker; Eric Rimm; Lynda M Rose; Christian M Shaffer; Clemens Schafmayer; Rulla M Tamimi; André G Uitterlinden; Uwe Völker; Henry Völzke; Yoshiyuki Wakabayashi; Janey L Wiggs; Jun Zhu; Dan M Roden; Bruno H Stricker; Weihong Tang; Alexander Teumer; Jochen Hampe; Anne Tybjærg-Hansen; Daniel I Chasman; Andrew T Chan; Andrew D Johnson
Journal:  Gastroenterology       Date:  2016-04-16       Impact factor: 22.682

5.  Potential causal role of l-glutamine in sickle cell disease painful crises: A Mendelian randomization analysis.

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Journal:  Blood Cells Mol Dis       Date:  2020-09-10       Impact factor: 3.039

6.  Bilirubin as a potential causal factor in type 2 diabetes risk: a Mendelian randomization study.

Authors:  Ali Abbasi; Petronella E Deetman; Eva Corpeleijn; Ron T Gansevoort; Rijk O B Gans; Hans L Hillege; Pim van der Harst; Ronald P Stolk; Gerjan Navis; Behrooz Z Alizadeh; Stephan J L Bakker
Journal:  Diabetes       Date:  2014-11-03       Impact factor: 9.461

7.  Pleiotropic associations of heterozygosity for the SERPINA1 Z allele in the UK Biobank.

Authors:  Katherine A Fawcett; Kijoung Song; Guoqing Qian; Aliki-Eleni Farmaki; Richard Packer; Catherine John; Nick Shrine; Raquel Granell; Sue Ring; Nicholas J Timpson; Laura M Yerges-Armstrong; Richard Eastell; Louise V Wain; Robert A Scott; Martin D Tobin; Ian P Hall
Journal:  ERJ Open Res       Date:  2021-05-10

8.  The prevalence and risk factors for gallstone disease in taiwanese vegetarians.

Authors:  Yen-Chun Chen; Chia Chiou; Ming-Nan Lin; Chin-Lon Lin
Journal:  PLoS One       Date:  2014-12-18       Impact factor: 3.240

Review 9.  Causal relationship from coffee consumption to diseases and mortality: a review of observational and Mendelian randomization studies including cardiometabolic diseases, cancer, gallstones and other diseases.

Authors:  Ask T Nordestgaard
Journal:  Eur J Nutr       Date:  2021-07-28       Impact factor: 5.614

10.  Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease.

Authors:  Julia Kozlitina; Eriks Smagris; Stefan Stender; Børge G Nordestgaard; Heather H Zhou; Anne Tybjærg-Hansen; Thomas F Vogt; Helen H Hobbs; Jonathan C Cohen
Journal:  Nat Genet       Date:  2014-02-16       Impact factor: 38.330

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