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dc.contributor.authorSchaefer, Arne S.
dc.contributor.authorBochenek, Gregor
dc.contributor.authorJochens, Arne
dc.contributor.authorEllinghaus, David
dc.contributor.authorDommisch, Henrik
dc.contributor.authorGuezeldemir-Akcakanat, Esra
dc.contributor.authorGraetz, Christian
dc.contributor.authorHarks, Inga
dc.contributor.authorJockel-Schneider, Yvonne
dc.contributor.authorWeinspach, Knut
dc.contributor.authorMeyle, Joerg
dc.contributor.authorEickholz, Peter
dc.contributor.authorLinden, Gerry J.
dc.contributor.authorCine, Naci
dc.contributor.authorNohutcu, Rahime
dc.contributor.authorWeiss, Ervin
dc.contributor.authorHouri-Haddad, Yael
dc.contributor.authorIraqi, Fuad
dc.contributor.authorFolwaczny, Mathias
dc.contributor.authorNoack, Barbara
dc.contributor.authorStrauch, Konstantin
dc.contributor.authorGieger, Christian
dc.contributor.authorWaldenberger, Melanie
dc.contributor.authorPeters, Annette
dc.contributor.authorWijmenga, Cisca
dc.contributor.authorYilmaz, Engin
dc.contributor.authorLieb, Wolfgang
dc.contributor.authorRosenstiel, Philip
dc.contributor.authorDoerfer, Christof
dc.contributor.authorBruckmann, Corinna
dc.contributor.authorErdmann, Jeannette
dc.contributor.authorKoenig, Inke
dc.contributor.authorJepsen, Soren
dc.contributor.authorLoos, Bruno G.
dc.contributor.authorSchreiber, Stefan
dc.date.accessioned2019-12-16T06:53:30Z
dc.date.available2019-12-16T06:53:30Z
dc.date.issued2015
dc.identifier.issn1942-325X
dc.identifier.urihttps://doi.org/10.1161/CIRCGENETICS.114.000554
dc.identifier.urihttp://hdl.handle.net/11655/19121
dc.description.abstractBackground-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, 1448 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=5.9x10(-5); odds ratio, 1.27; 95% confidence interval, 1.3-1.4 [adjusted for smoking and sex]; 818 cases; 5309 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; odds ratio, 1.27 [95% confidence interval, 1.1-1.5]; 703 cases; 2.143 controls) and CAD (P=0.0003; odds ratio, 0.84 [95% confidence interval, 0.8-0.9]; n=4117 cases; 5824 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 transforming growth factor-beta 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 transforming growth factor-beta signaling.
dc.language.isoen
dc.publisherLippincott Williams & Wilkins
dc.relation.isversionof10.1161/CIRCGENETICS.114.000554
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCardiovascular System & Cardiology
dc.subjectGenetics & Heredity
dc.titleGenetic Evidence For Plasminogen As A Shared Genetic Risk Factor Of Coronary Artery Disease And Periodontitis
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalCirculation-Cardiovascular Genetics
dc.contributor.departmentPeriodontoloji
dc.identifier.volume8
dc.identifier.issue1
dc.identifier.startpage159
dc.identifier.endpage167
dc.description.indexWoS
dc.description.indexScopus


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