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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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Detalles Bibliográficos
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
Descripción
Sumario: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.