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Wild, P.S.* ; Zeller, T.* ; Schillert, A.* ; Szymczak, S.* ; Sinning, C.R.* ; Deiseroth, A.* ; Schnabel, R.B.* ; Lubos, E.* ; Keller, T.* ; Eleftheriadis, M.S.* ; Bickel, C.* ; Rupprecht, H.J.* ; Wilde, S.* ; Rossmann, H.* ; Diemert, P.* ; Cupples, L.A.* ; Perret, C.* ; Erdmann, J.* ; Stark, K.* ; Kleber, M.E.* ; Epstein, S.E.* ; Voight, B.F.* ; Kuulasmaa, K.* ; Li, M.* ; Schäfer, A.S.* ; Klopp, N. ; Braund, P.S.* ; Sager, H.B.* ; Demissie, S.* ; Proust, C.* ; König, I.R.* ; Wichmann, H.-E. ; Reinhard, W.* ; Hoffmann, M.M.* ; Virtamo, J.* ; Burnett, M.S.* ; Siscovick, D.* ; Wiklund, P.G.* ; Qu, L.* ; El Mokthari, N.E.* ; Thompson, J.R.* ; Peters, A. ; Smith, A.V.* ; Yon, E.* ; Baumert, J.J. ; Hengstenberg, C.* ; Marz, W.* ; Amouyel, P.* ; Devaney, J.* ; Schwartz, S.M.* ; Saarela, O.* ; Mehta, N.N.* ; Rubin, D.* ; Silander, K.* ; Hall, A.S.* ; Ferrieres, J.* ; Harris, T.B.* ; Melander, O.* ; Kee, F.* ; Hakonarson, H.* ; Schrezenmeir, J.* ; Gudnason, V.* ; Elosua, R.* ; Arveiler, D.* ; Evans, A.* ; Rader, D.J.* ; Illig, T. ; Schreiber, S.* ; Bis, J.C.* ; Altshuler, D.* ; Kavousi, M.* ; Witteman, J.C.* ; Uitterlinden, A.G.* ; Hofman, A.* ; Folsom, A.R.* ; Barbalic, M.* ; Boerwinkle, E.* ; Kathiresan, S.* ; Reilly, M.P.* ; O'Donnell, C.J.* ; Samani, N.J.* ; Schunkert, H.* ; Cambien, F.* ; Lackner, K.J.* ; Tiret, L.* ; Salomaa, V.* ; Münzel, T.* ; Ziegler, A.* ; Blankenberg, S.*

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

Circ. Cardiovasc. Genet. 4, 403-412 (2011)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
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.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter coronary artery disease; genome-wide association studies; gene expression; genetic variation; genomics; eQTL; eSNP; LIPA
ISSN (print) / ISBN 1942-325X
e-ISSN 1942-3268
Zeitschrift Circulation: Cardiovascular Genetics
Quellenangaben Band: 4, Heft: 4, Seiten: 403-412 Artikelnummer: , Supplement: ,
Verlag Lippincott Williams & Wilkins
Verlagsort Hagerstown, Md
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Research Unit Molecular Epidemiology (AME)
Institute of Epidemiology II (EPI2)