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A Genome-Wide Association Study of Circulating Galectin-3

Galectin-3 is a lectin involved in fibrosis, inflammation and proliferation. Increased circulating levels of galectin-3 have been associated with various diseases, including cancer, immunological disorders, and cardiovascular disease. To enhance our knowledge on galectin-3 biology we performed the f...

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Autores principales: de Boer, Rudolf A., Verweij, Niek, van Veldhuisen, Dirk J., Westra, Harm-Jan, Bakker, Stephan J. L., Gansevoort, Ron T., Muller Kobold, Anneke C., van Gilst, Wiek H., Franke, Lude, Leach, Irene Mateo, van der Harst, Pim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467202/
https://www.ncbi.nlm.nih.gov/pubmed/23056639
http://dx.doi.org/10.1371/journal.pone.0047385
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author de Boer, Rudolf A.
Verweij, Niek
van Veldhuisen, Dirk J.
Westra, Harm-Jan
Bakker, Stephan J. L.
Gansevoort, Ron T.
Muller Kobold, Anneke C.
van Gilst, Wiek H.
Franke, Lude
Leach, Irene Mateo
van der Harst, Pim
author_facet de Boer, Rudolf A.
Verweij, Niek
van Veldhuisen, Dirk J.
Westra, Harm-Jan
Bakker, Stephan J. L.
Gansevoort, Ron T.
Muller Kobold, Anneke C.
van Gilst, Wiek H.
Franke, Lude
Leach, Irene Mateo
van der Harst, Pim
author_sort de Boer, Rudolf A.
collection PubMed
description Galectin-3 is a lectin involved in fibrosis, inflammation and proliferation. Increased circulating levels of galectin-3 have been associated with various diseases, including cancer, immunological disorders, and cardiovascular disease. To enhance our knowledge on galectin-3 biology we performed the first genome-wide association study (GWAS) using the Illumina HumanCytoSNP-12 array imputed with the HapMap 2 CEU panel on plasma galectin-3 levels in 3,776 subjects and follow-up genotyping in an additional 3,516 subjects. We identified 2 genome wide significant loci associated with plasma galectin-3 levels. One locus harbours the LGALS3 gene (rs2274273; P = 2.35×10(−188)) and the other locus the ABO gene (rs644234; P = 3.65×10(−47)). The variance explained by the LGALS3 locus was 25.6% and by the ABO locus 3.8% and jointly they explained 29.2%. Rs2274273 lies in high linkage disequilibrium with two non-synonymous SNPs (rs4644; r(2) = 1.0, and rs4652; r(2) = 0.91) and wet lab follow-up genotyping revealed that both are strongly associated with galectin-3 levels (rs4644; P = 4.97×10(−465) and rs4652 P = 1.50×10(−421)) and were also associated with LGALS3 gene-expression. The origins of our associations should be further validated by means of functional experiments.
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spelling pubmed-34672022012-10-10 A Genome-Wide Association Study of Circulating Galectin-3 de Boer, Rudolf A. Verweij, Niek van Veldhuisen, Dirk J. Westra, Harm-Jan Bakker, Stephan J. L. Gansevoort, Ron T. Muller Kobold, Anneke C. van Gilst, Wiek H. Franke, Lude Leach, Irene Mateo van der Harst, Pim PLoS One Research Article Galectin-3 is a lectin involved in fibrosis, inflammation and proliferation. Increased circulating levels of galectin-3 have been associated with various diseases, including cancer, immunological disorders, and cardiovascular disease. To enhance our knowledge on galectin-3 biology we performed the first genome-wide association study (GWAS) using the Illumina HumanCytoSNP-12 array imputed with the HapMap 2 CEU panel on plasma galectin-3 levels in 3,776 subjects and follow-up genotyping in an additional 3,516 subjects. We identified 2 genome wide significant loci associated with plasma galectin-3 levels. One locus harbours the LGALS3 gene (rs2274273; P = 2.35×10(−188)) and the other locus the ABO gene (rs644234; P = 3.65×10(−47)). The variance explained by the LGALS3 locus was 25.6% and by the ABO locus 3.8% and jointly they explained 29.2%. Rs2274273 lies in high linkage disequilibrium with two non-synonymous SNPs (rs4644; r(2) = 1.0, and rs4652; r(2) = 0.91) and wet lab follow-up genotyping revealed that both are strongly associated with galectin-3 levels (rs4644; P = 4.97×10(−465) and rs4652 P = 1.50×10(−421)) and were also associated with LGALS3 gene-expression. The origins of our associations should be further validated by means of functional experiments. Public Library of Science 2012-10-09 /pmc/articles/PMC3467202/ /pubmed/23056639 http://dx.doi.org/10.1371/journal.pone.0047385 Text en © 2012 de Boer 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
de Boer, Rudolf A.
Verweij, Niek
van Veldhuisen, Dirk J.
Westra, Harm-Jan
Bakker, Stephan J. L.
Gansevoort, Ron T.
Muller Kobold, Anneke C.
van Gilst, Wiek H.
Franke, Lude
Leach, Irene Mateo
van der Harst, Pim
A Genome-Wide Association Study of Circulating Galectin-3
title A Genome-Wide Association Study of Circulating Galectin-3
title_full A Genome-Wide Association Study of Circulating Galectin-3
title_fullStr A Genome-Wide Association Study of Circulating Galectin-3
title_full_unstemmed A Genome-Wide Association Study of Circulating Galectin-3
title_short A Genome-Wide Association Study of Circulating Galectin-3
title_sort genome-wide association study of circulating galectin-3
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467202/
https://www.ncbi.nlm.nih.gov/pubmed/23056639
http://dx.doi.org/10.1371/journal.pone.0047385
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