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

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 reproduc...

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Autores principales: Karakas, Mahir, Baumert, Jens, Kleber, Marcus E., Thorand, Barbara, Dallmeier, Dhayana, Silbernagel, Günther, Grammer, Tanja B., Rottbauer, Wolfgang, Meisinger, Christa, Illig, Thomas, März, Winfried, Koenig, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532506/
https://www.ncbi.nlm.nih.gov/pubmed/23300549
http://dx.doi.org/10.1371/journal.pone.0051441
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author Karakas, Mahir
Baumert, Jens
Kleber, Marcus E.
Thorand, Barbara
Dallmeier, Dhayana
Silbernagel, Günther
Grammer, Tanja B.
Rottbauer, Wolfgang
Meisinger, Christa
Illig, Thomas
März, Winfried
Koenig, Wolfgang
author_facet Karakas, Mahir
Baumert, Jens
Kleber, Marcus E.
Thorand, Barbara
Dallmeier, Dhayana
Silbernagel, Günther
Grammer, Tanja B.
Rottbauer, Wolfgang
Meisinger, Christa
Illig, Thomas
März, Winfried
Koenig, Wolfgang
author_sort Karakas, Mahir
collection PubMed
description 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 = 1.87×10(−103)) in KORA and −0.35 ng/ml (p = 5.11×10(−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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spelling pubmed-35325062013-01-08 A Variant In the Abo Gene Explains the Variation in Soluble E-Selectin Levels—Results from Dense Genotyping in Two Independent Populations Karakas, Mahir Baumert, Jens Kleber, Marcus E. Thorand, Barbara Dallmeier, Dhayana Silbernagel, Günther Grammer, Tanja B. Rottbauer, Wolfgang Meisinger, Christa Illig, Thomas März, Winfried Koenig, Wolfgang PLoS One Research Article 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 = 1.87×10(−103)) in KORA and −0.35 ng/ml (p = 5.11×10(−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. Public Library of Science 2012-12-28 /pmc/articles/PMC3532506/ /pubmed/23300549 http://dx.doi.org/10.1371/journal.pone.0051441 Text en © 2012 Karakas et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Karakas, Mahir
Baumert, Jens
Kleber, Marcus E.
Thorand, Barbara
Dallmeier, Dhayana
Silbernagel, Günther
Grammer, Tanja B.
Rottbauer, Wolfgang
Meisinger, Christa
Illig, Thomas
März, Winfried
Koenig, Wolfgang
A Variant In the Abo Gene Explains the Variation in Soluble E-Selectin Levels—Results from Dense Genotyping in Two Independent Populations
title A Variant In the Abo Gene Explains the Variation in Soluble E-Selectin Levels—Results from Dense Genotyping in Two Independent Populations
title_full A Variant In the Abo Gene Explains the Variation in Soluble E-Selectin Levels—Results from Dense Genotyping in Two Independent Populations
title_fullStr A Variant In the Abo Gene Explains the Variation in Soluble E-Selectin Levels—Results from Dense Genotyping in Two Independent Populations
title_full_unstemmed A Variant In the Abo Gene Explains the Variation in Soluble E-Selectin Levels—Results from Dense Genotyping in Two Independent Populations
title_short A Variant In the Abo Gene Explains the Variation in Soluble E-Selectin Levels—Results from Dense Genotyping in Two Independent Populations
title_sort variant in the abo gene explains the variation in soluble e-selectin levels—results from dense genotyping in two independent populations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532506/
https://www.ncbi.nlm.nih.gov/pubmed/23300549
http://dx.doi.org/10.1371/journal.pone.0051441
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