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Schäfer, A.S.* ; Bochenek, G.* ; Jochens, A.* ; Ellinghaus, D.* ; Dommisch, H.* ; Guzeldemir-Akcakana, E.* ; Graetz, C.* ; Harks, I.* ; Jockel-Schneider, Y.* ; Weinspach, K.* ; Meyle, J.* ; Eickholz, P.* ; Linden, G.J.* ; Cine, N.* ; Nohutcu, R.* ; Weiss, E.* ; Houri-Haddad, Y.* ; Iraqi, F.* ; Folwaczny, M.* ; Noack, B.* ; Strauch, K. ; Gieger, C. ; Waldenberger, M. ; Peters, A. ; Wijmenga, C.* ; Yilmaz, E.* ; Lieb, W.* ; Rosenstiel, P.* ; Doerfer, C.* ; Bruckmann, C.* ; Erdmann, J.* ; König, I.* ; Jepsen, S.* ; Loos, B.G.* ; Schreiber, S.*

Genetic evidence for PLASMINOGEN as a shared genetic risk factor of coronary artery disease and periodontitis.

Circ. Cardiovasc. Genet. 8, 159-167 (2015)
Verlagsversion DOI PMC
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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
BACKGROUND: -Genetic studies demonstrated the presence of risk alleles in the genes ANRIL and CAMTA1/VAMP3 that are shared between coronary artery disease (CAD) and periodontitis. We aimed to identify further shared genetic risk factors to better understand conjoint disease mechanisms. METHODS AND RESULTS: -In-depth genotyping of 46 published CAD risk loci of genome-wide significance in the worldwide largest case-control sample of the severe early-onset phenotype aggressive periodontitis (AgP) with the Illumina Immunochip (600 German AgP cases, 1,448 controls) and the Affymetrix 500K array set (283 German AgP cases and 972 controls) highlighted ANRIL as the major risk gene and revealed further associations with AgP for the gene PLASMINOGEN (PLG) (rs4252120, P=5.9×10(-5), OR=1.27, 95% CI=1.3-1.4 [adjusted for smoking and sex]; 818 cases, 5,309 controls). Subsequent combined analyses of several genome-wide data sets of CAD and AgP suggested TGFBRAP1 to be associated with AgP (rs2679895 P=0.0016, OR=1.27 [95% CI=1.1-1.5]; 703 cases, 2.143 controls) and CAD (P=0.0003, OR=0.84 [95% CI=0.8-0.9]; N=4,117 cases, 5,824 controls). The study further provides evidence that in addition to PLG, the currently known shared susceptibility loci of CAD and periodontitis, ANRIL and CAMTA1/VAMP3, are subjected to TGF-β regulation. CONCLUSIONS: -PLG is the third replicated shared genetic risk factor of atherosclerosis and periodontitis. All known shared risk genes of CAD and periodontitis are members of TGF-β signaling.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Association Study ; Coronary Artery Disease ; Genetic Association ; Periodontitis ; Plasminogen; Genome-wide Association; Factor-beta Receptor; Susceptibility Locus; Tgf-beta; Activation; Replication; Atherosclerosis; Inflammation; Populations; 9p21.3
Sprache englisch
Veröffentlichungsjahr 2015
Prepublished im Jahr 2014
HGF-Berichtsjahr 2014
ISSN (print) / ISBN 1942-325X
e-ISSN 1942-3268
Zeitschrift Circulation: Cardiovascular Genetics
Quellenangaben Band: 8, Heft: 1, Seiten: 159-167 Artikelnummer: , Supplement: ,
Verlag Lippincott Williams & Wilkins
Verlagsort Hagerstown, Md
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Genetic Epidemiology (IGE)
Institute of Epidemiology (EPI)
POF Topic(s) 30501 - Systemic Analysis of Genetic and Environmental Factors that Impact Health
30202 - Environmental Health
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-504100-001
G-504091-004
G-504091-001
G-504000-001
PubMed ID 25466412
DOI 10.1161/CIRCGENETICS.114.000554
WOS ID WOS:000349873200021
Scopus ID 84924544016
Erfassungsdatum 2014-12-05
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