Literature DB >> 21606135

A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.

Philipp S Wild1, Tanja Zeller, Arne Schillert, Silke Szymczak, Christoph R Sinning, Arne Deiseroth, Renate B Schnabel, Edith Lubos, Till Keller, Medea S Eleftheriadis, Christoph Bickel, Hans J Rupprecht, Sandra Wilde, Heidi Rossmann, Patrick Diemert, L Adrienne Cupples, Claire Perret, Jeanette Erdmann, Klaus Stark, Marcus E Kleber, Stephen E Epstein, Benjamin F Voight, Kari Kuulasmaa, Mingyao Li, Arne S Schäfer, Norman Klopp, Peter S Braund, Hendrik B Sager, Serkalem Demissie, Carole Proust, Inke R König, Heinz-Erich Wichmann, Wibke Reinhard, Michael M Hoffmann, Jarmo Virtamo, Mary Susan Burnett, David Siscovick, Per Gunnar Wiklund, Liming Qu, Nour Eddine El Mokthari, John R Thompson, Annette Peters, Albert V Smith, Emmanuelle Yon, Jens Baumert, Christian Hengstenberg, Winfried März, Philippe Amouyel, Joseph Devaney, Stephen M Schwartz, Olli Saarela, Nehal N Mehta, Diana Rubin, Kaisa Silander, Alistair S Hall, Jean Ferrieres, Tamara B Harris, Olle Melander, Frank Kee, Hakon Hakonarson, Juergen Schrezenmeir, Vilmundur Gudnason, Roberto Elosua, Dominique Arveiler, Alun Evans, Daniel J Rader, Thomas Illig, Stefan Schreiber, Joshua C Bis, David Altshuler, Maryam Kavousi, Jaqueline C M Witteman, Andre G Uitterlinden, Albert Hofman, Aaron R Folsom, Maja Barbalic, Eric Boerwinkle, Sekar Kathiresan, Muredach P Reilly, Christopher J O'Donnell, Nilesh J Samani, Heribert Schunkert, Francois Cambien, Karl J Lackner, Laurence Tiret, Veikko Salomaa, Thomas Munzel, Andreas Ziegler, Stefan Blankenberg.   

Abstract

BACKGROUND: eQTL analyses are important to improve the understanding of genetic association results. We performed a genome-wide association and global gene expression study to identify functionally relevant variants affecting the risk of coronary artery disease (CAD). METHODS AND
RESULTS: In a genome-wide association analysis of 2078 CAD cases and 2953 control subjects, we identified 950 single-nucleotide polymorphisms (SNPs) that were associated with CAD at P<10(-3). Subsequent in silico and wet-laboratory replication stages and a final meta-analysis of 21 428 CAD cases and 38 361 control subjects revealed a novel association signal at chromosome 10q23.31 within the LIPA (lysosomal acid lipase A) gene (P=3.7×10(-8); odds ratio, 1.1; 95% confidence interval, 1.07 to 1.14). The association of this locus with global gene expression was assessed by genome-wide expression analyses in the monocyte transcriptome of 1494 individuals. The results showed a strong association of this locus with expression of the LIPA transcript (P=1.3×10(-96)). An assessment of LIPA SNPs and transcript with cardiovascular phenotypes revealed an association of LIPA transcript levels with impaired endothelial function (P=4.4×10(-3)).
CONCLUSIONS: The use of data on genetic variants and the addition of data on global monocytic gene expression led to the identification of the novel functional CAD susceptibility locus LIPA, located on chromosome 10q23.31. The respective eSNPs associated with CAD strongly affect LIPA gene expression level, which was related to endothelial dysfunction, a precursor of CAD.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21606135      PMCID: PMC3157552          DOI: 10.1161/CIRCGENETICS.110.958728

Source DB:  PubMed          Journal:  Circ Cardiovasc Genet        ISSN: 1942-3268


  33 in total

1.  GenABEL: an R library for genome-wide association analysis.

Authors:  Yurii S Aulchenko; Stephan Ripke; Aaron Isaacs; Cornelia M van Duijn
Journal:  Bioinformatics       Date:  2007-03-23       Impact factor: 6.937

2.  A common variant on chromosome 9p21 affects the risk of myocardial infarction.

Authors:  Anna Helgadottir; Gudmar Thorleifsson; Andrei Manolescu; Solveig Gretarsdottir; Thorarinn Blondal; Aslaug Jonasdottir; Adalbjorg Jonasdottir; Asgeir Sigurdsson; Adam Baker; Arnar Palsson; Gisli Masson; Daniel F Gudbjartsson; Kristinn P Magnusson; Karl Andersen; Allan I Levey; Valgerdur M Backman; Sigurborg Matthiasdottir; Thorbjorg Jonsdottir; Stefan Palsson; Helga Einarsdottir; Steinunn Gunnarsdottir; Arnaldur Gylfason; Viola Vaccarino; W Craig Hooper; Muredach P Reilly; Christopher B Granger; Harland Austin; Daniel J Rader; Svati H Shah; Arshed A Quyyumi; Jeffrey R Gulcher; Gudmundur Thorgeirsson; Unnur Thorsteinsdottir; Augustine Kong; Kari Stefansson
Journal:  Science       Date:  2007-05-03       Impact factor: 47.728

Review 3.  Overexpression of lysosomal acid lipase and other proteins in atherosclerosis.

Authors:  Oliver Zschenker; Till Illies; Detlev Ameis
Journal:  J Biochem       Date:  2006-07       Impact factor: 3.387

4.  A common allele on chromosome 9 associated with coronary heart disease.

Authors:  Ruth McPherson; Alexander Pertsemlidis; Nihan Kavaslar; Alexandre Stewart; Robert Roberts; David R Cox; David A Hinds; Len A Pennacchio; Anne Tybjaerg-Hansen; Aaron R Folsom; Eric Boerwinkle; Helen H Hobbs; Jonathan C Cohen
Journal:  Science       Date:  2007-05-03       Impact factor: 47.728

5.  Relative impact of nucleotide and copy number variation on gene expression phenotypes.

Authors:  Barbara E Stranger; Matthew S Forrest; Mark Dunning; Catherine E Ingle; Claude Beazley; Natalie Thorne; Richard Redon; Christine P Bird; Anna de Grassi; Charles Lee; Chris Tyler-Smith; Nigel Carter; Stephen W Scherer; Simon Tavaré; Panagiotis Deloukas; Matthew E Hurles; Emmanouil T Dermitzakis
Journal:  Science       Date:  2007-02-09       Impact factor: 47.728

6.  In situ localization of the genetic locus encoding the lysosomal acid lipase/cholesteryl esterase (LIPA) deficient in Wolman disease to chromosome 10q23.2-q23.3.

Authors:  R A Anderson; N Rao; R S Byrum; C B Rothschild; D W Bowden; R Hayworth; M Pettenati
Journal:  Genomics       Date:  1993-01       Impact factor: 5.736

7.  A splice junction mutation causes deletion of a 72-base exon from the mRNA for lysosomal acid lipase in a patient with cholesteryl ester storage disease.

Authors:  H Klima; K Ullrich; C Aslanidis; P Fehringer; K J Lackner; G Schmitz
Journal:  J Clin Invest       Date:  1993-12       Impact factor: 14.808

8.  Genetic and biochemical evidence that CESD and Wolman disease are distinguished by residual lysosomal acid lipase activity.

Authors:  C Aslanidis; S Ries; P Fehringer; C Büchler; H Klima; G Schmitz
Journal:  Genomics       Date:  1996-04-01       Impact factor: 5.736

9.  Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

Authors: 
Journal:  Nature       Date:  2007-06-07       Impact factor: 49.962

10.  Genomewide association analysis of coronary artery disease.

Authors:  Nilesh J Samani; Jeanette Erdmann; Alistair S Hall; Christian Hengstenberg; Massimo Mangino; Bjoern Mayer; Richard J Dixon; Thomas Meitinger; Peter Braund; H-Erich Wichmann; Jennifer H Barrett; Inke R König; Suzanne E Stevens; Silke Szymczak; David-Alexandre Tregouet; Mark M Iles; Friedrich Pahlke; Helen Pollard; Wolfgang Lieb; Francois Cambien; Marcus Fischer; Willem Ouwehand; Stefan Blankenberg; Anthony J Balmforth; Andrea Baessler; Stephen G Ball; Tim M Strom; Ingrid Braenne; Christian Gieger; Panos Deloukas; Martin D Tobin; Andreas Ziegler; John R Thompson; Heribert Schunkert
Journal:  N Engl J Med       Date:  2007-07-18       Impact factor: 91.245

View more
  65 in total

Review 1.  Understanding the genetics of coronary artery disease through the lens of noninvasive imaging.

Authors:  Eunice Yang; Jose D Vargas; David A Bluemke
Journal:  Expert Rev Cardiovasc Ther       Date:  2012-01

Review 2.  Genetics of human cardiovascular disease.

Authors:  Sekar Kathiresan; Deepak Srivastava
Journal:  Cell       Date:  2012-03-16       Impact factor: 41.582

3.  Prediction of Causal Candidate Genes in Coronary Artery Disease Loci.

Authors:  Ingrid Brænne; Mete Civelek; Baiba Vilne; Antonio Di Narzo; Andrew D Johnson; Yuqi Zhao; Benedikt Reiz; Veronica Codoni; Thomas R Webb; Hassan Foroughi Asl; Stephen E Hamby; Lingyao Zeng; David-Alexandre Trégouët; Ke Hao; Eric J Topol; Eric E Schadt; Xia Yang; Nilesh J Samani; Johan L M Björkegren; Jeanette Erdmann; Heribert Schunkert; Aldons J Lusis
Journal:  Arterioscler Thromb Vasc Biol       Date:  2015-08-20       Impact factor: 8.311

4.  Single nucleotide polymorphisms in an intergenic chromosome 2q region associated with tissue factor pathway inhibitor plasma levels and venous thromboembolism.

Authors:  J Dennis; V Truong; D Aïssi; A Medina-Rivera; S Blankenberg; M Germain; M Lemire; L Antounians; M Civelek; R Schnabel; P Wells; M D Wilson; P-E Morange; D-A Trégouët; F Gagnon
Journal:  J Thromb Haemost       Date:  2016-09-17       Impact factor: 5.824

5.  Linkage analysis incorporating gene-age interactions identifies seven novel lipid loci: the Family Blood Pressure Program.

Authors:  Jeannette Simino; Rezart Kume; Aldi T Kraja; Stephen T Turner; Craig L Hanis; Wayne Sheu; Ida Chen; Cashell Jaquish; Richard S Cooper; Aravinda Chakravarti; Thomas Quertermous; Eric Boerwinkle; Steven C Hunt; D C Rao
Journal:  Atherosclerosis       Date:  2014-04-26       Impact factor: 5.162

Review 6.  Lysosomal acid lipase and lipid metabolism: new mechanisms, new questions, and new therapies.

Authors:  Hanrui Zhang
Journal:  Curr Opin Lipidol       Date:  2018-06       Impact factor: 4.776

7.  Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four US populations: the Population Architecture using Genomics and Epidemiology (PAGE) study.

Authors:  Lili Zhang; Petra Buzkova; Christina L Wassel; Mary J Roman; Kari E North; Dana C Crawford; Jonathan Boston; Kristin D Brown-Gentry; Shelley A Cole; Ewa Deelman; Robert Goodloe; Sarah Wilson; Gerardo Heiss; Nancy S Jenny; Neal W Jorgensen; Tara C Matise; Bob E McClellan; Alejandro Q Nato; Marylyn D Ritchie; Nora Franceschini; W H Linda Kao
Journal:  Atherosclerosis       Date:  2013-03-13       Impact factor: 5.162

8.  Physiological difference in autophagic flux in macrophages from 2 mouse strains regulates cholesterol ester metabolism.

Authors:  Peggy Robinet; Brian Ritchey; Jonathan D Smith
Journal:  Arterioscler Thromb Vasc Biol       Date:  2013-03-14       Impact factor: 8.311

9.  Frequency of the cholesteryl ester storage disease common LIPA E8SJM mutation (c.894G>A) in various racial and ethnic groups.

Authors:  Stuart A Scott; Benny Liu; Irina Nazarenko; Suparna Martis; Julia Kozlitina; Yao Yang; Charina Ramirez; Yumi Kasai; Tommy Hyatt; Inga Peter; Robert J Desnick
Journal:  Hepatology       Date:  2013-07-29       Impact factor: 17.425

Review 10.  Genetics of coronary artery disease and myocardial infarction--2013.

Authors:  Thorsten Kessler; Jeanette Erdmann; Heribert Schunkert
Journal:  Curr Cardiol Rep       Date:  2013-06       Impact factor: 2.931

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.