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    Título
    VAV3 Gene Polymorphism Is Associated with Paget's Disease of Bone
    Autor(es)
    Usategui-Martín, Ricardo
    Calero-Paniagua, Ismael
    García Aparicio, JuditUSAL authority
    Corral Gudino, Luís
    Pino Montes, Javier delUSAL authority ORCID
    González Sarmiento, RogelioUSAL authority ORCID
    Palabras clave
    Paget's Disease of Bone
    Gene Polymorphism
    Clasificación UNESCO
    3209 Farmacología
    Fecha de publicación
    2016
    Editor
    Mary Ann Liebert
    Citación
    Usategui-Martín, R., Calero-Paniagua, I., García-Aparicio, J., Corral-Gudino, L., del Pino Montes, J., & González Sarmiento, R. (2016). VAV3 Gene Polymorphism Is Associated with Paget's Disease of Bone. Genetic Testing and Molecular Biomarkers, 20(6), 335-337.
    Resumen
    [EN]Background and aims: Paget's disease of bone (PDB) is a focal bone disorder affecting the skeleton segmentally. The disease affects osteoclasts which increase in size, number, and activity. One of the etiopathogenic hypotheses is that the disease is genetic. It has been reported that Rho GEF Vav3 is an essential factor in the regulation of osteoclast function, and alteration of the VAV3 gene could influence the development of the disease. The aim of our study was to perform an association study between variants of the VAV3 gene and the risk of developing Paget's disease of bone. Patients and methods: The genotypic and allelic distribution of the VAV3 c.892A>T/p.T298S (rs7528153) polymorphism was compared between a cohort of 238 Spanish subjects with PDB and a cohort of 253 healthy subjects. Results: Our results indicated that individuals carrying the VAV3 rs7528153 TT genotype were at a significantly increased risk of developing PDB (p < 0.001, odds ratio [OR] = 3.15, 95% confidence interval [95% CI] = 1.77-5.61). Conclusions: These results suggest that inheriting the VAV3 rs7528153 polymorphism is a likely susceptibility factor for developing Paget's disease of bone.
    URI
    https://hdl.handle.net/10366/162467
    ISSN
    1945-0265
    DOI
    10.1089/gtmb.2015.0292
    Versión del editor
    https://doi.org/10.1089/gtmb.2015.0292
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    • DFIFA. Artículos del Departamento de Fisiología y Farmacología [151]
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