A Variant In the Abo Gene Explains the Variation in Soluble E-Selectin Levels-Results from Dense Genotyping in Two Independent Populations

被引:33
作者
Karakas, Mahir [1 ]
Baumert, Jens [2 ]
Kleber, Marcus E. [1 ,3 ]
Thorand, Barbara [2 ]
Dallmeier, Dhayana [1 ]
Silbernagel, Guenther [4 ]
Grammer, Tanja B. [3 ]
Rottbauer, Wolfgang [1 ]
Meisinger, Christa [2 ]
Illig, Thomas [5 ,6 ]
Maerz, Winfried [3 ,7 ,8 ]
Koenig, Wolfgang [1 ]
机构
[1] Univ Ulm, Med Ctr, Dept Internal Med Cardiol 2, Ulm, Germany
[2] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Inst Epidemiol 2, Neuherberg, Germany
[3] Heidelberg Univ, Med Fac Mannheim, Mannheim Inst Publ Hlth Social & Prevent Med, D-6800 Mannheim, Germany
[4] Univ Tubingen, Dept Internal Med, Div Endocrinol Diabetol Nephrol Vasc Dis & Clin C, D-7400 Tubingen, Germany
[5] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Res Unit Mol Epidemiol, Neuherberg, Germany
[6] Hannover Med Sch, Hannover Unified Biobank, D-3000 Hannover, Germany
[7] Med Univ Graz, Clin Inst Med & Chem Lab Diagnost, Graz, Austria
[8] Synlab Serv GmbH, Synlab Acad, Mannheim, Germany
关键词
INTERCELLULAR-ADHESION MOLECULE-1; RISK; DISEASE; ASSOCIATION; HEART; LOCI; ATHEROSCLEROSIS;
D O I
10.1371/journal.pone.0051441
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Elevated soluble (s) E-selectin levels have been associated with various cardiovascular diseases. Recently, genetic variants in the ABO blood group have been related to E-selectin levels in a small cohort of patients with type 1 diabetes. We evaluated whether this association is reproducible in two large samples of Caucasians. Methodology/Principal Findings: Data of the present study was drawn from the population-based MONICA/KORA Augsburg study (n = 1,482) and the patients-based LURIC study (n = 1,546). A high-density genotyping array (50K IBC Chip) containing single-nucleotide polymorphisms (SNPs) from E-selectin candidate genes selected on known biology of E-selectin metabolism, mouse genetic studies, and human genetic association studies, was used for genotyping. Linear regression analyses with adjustment for age and sex (and survey in KORA) were applied to assess associations between gene variants and sE-selectin concentrations. A number of 12 SNPs (in KORA) and 13 SNPs (in LURIC), all from the ABO blood group gene, were significantly associated with the log-transformed concentration of E-selectin. The strongest association was observed for rs651007 with a change of log-transformed sE-selectin per one copy of the minor allele of -0.37 ng/ml (p = 1.87x10(-103)) in KORA and -0.35 ng/ml (p = 5.11x10(-84)) in LURIC. Inclusion of rs651007 increased the explained sE-selectin variance by 0.256 in KORA and 0.213 in LURIC. All SNPs had minor allele frequencies above 20% showing a substantial gene variation. Conclusions/Significance: Our findings in two independent samples indicate that the genetic variants at the ABO locus affect sE-selectin levels. Since distinct genome-wide association studies linked the ABO gene with myocardial infarction (MI) in the presence of coronary atherosclerosis and with coronary artery disease, these findings may not only enhance our understanding of adhesion molecule biology, but may also provide a focus for several novel research avenues.
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