3.8 Article

Genetic Evidence for PLASMINOGEN as a Shared Genetic Risk Factor of Coronary Artery Disease and Periodontitis

期刊

CIRCULATION-CARDIOVASCULAR GENETICS
卷 8, 期 1, 页码 159-167

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCGENETICS.114.000554

关键词

coronary artery disease; genetic association studies; periodontitis; plasminogen

资金

  1. research grant of the Research Center Inflammation Medicine of the Medical Faculty, Christian-Albrechts-University
  2. Deutsche Forschungsgemeinschaft [KFO208]
  3. Dutch Society of Periodontology
  4. research priority grant from the University of Amsterdam
  5. German Ministry for Education and Research [01EY1103]
  6. Helmholtz Zentrum M(sic)unchen-German Research Center for Environmental Health - German Federal Ministry of Education and Research
  7. State of Bavaria
  8. British Heart Foundation [PG/14/9/30632] Funding Source: researchfish
  9. Public Health Agency [RRG/3282/05] Funding Source: researchfish

向作者/读者索取更多资源

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, 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.

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