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    Título
    Val247Leu beta2-glycoprotein-I allelic variant is associated with antiphospholipid syndrome: Systematic review and meta-analysis
    Autor(es)
    Chamorro Fernández, Antonio JavierAutoridad USAL ORCID
    Marcos Martín, MiguelAutoridad USAL ORCID
    Mirón Canelo, José AntonioAutoridad USAL ORCID
    Cervera, R.
    Espinosa, G.
    Palabras clave
    Antiphospholipid syndrome
    Beta 2-Glycoprotein I
    Genetics
    Polymorphism
    Systematic review
    Meta-analysis
    Fecha de publicación
    2012
    Editor
    Elsevier
    Citación
    Chamorro, A. J., Marcos, M., Mirón-Canelo, J. A., Cervera, R., & Espinosa, G. (2012). Val247Leu beta2-glycoprotein-I allelic variant is associated with antiphospholipid syndrome: systematic review and meta-analysis. Autoimmunity reviews, 11(10), 705-712.
    Resumen
    [EN] Previous studies have suggested that the possession of the Val/Val genotype of the Val247Leu polymorphism of the β2-glycoproteinI (β2-GPI) gene may be associated with antiphospholipid syndrome (APS), and, among patients with APS, with the production of anti-β2-GPI antibodies or the development of thrombosis. Given the controversial results reported, the aim of this work is to combine previous findings by means of a systematic review and a meta-analysis. Methods: We retrieved studies analyzing the genotype of the above-mentioned polymorphism among patients with APS by means of electronic database search. A meta-analysis was conducted in a random effects model and calculations of odds ratio (OR) and confidence intervals (CI) were done. Sensitivity analysis and tests for heterogeneity of the results were performed. Results: Eight previous studies analyzed the association of APS, anti-β2-GPI antibodies and/or thrombosis with the Val247Leu polymorphism. After meta-analysis, patients with APS had a significantly higher prevalence of the Val/ Val genotype of this genetic variant when compared with controls (OR=2.04; 95% CI: 1.12, 3.73; P=0.02). Among patients with APS, those with anti-β2-GPI antibodies had a higher prevalence of this genotype (OR=1.73; 95% CI: 1.04, 2.87; P=0.03). No significant results were found for the presence of arterial or venous thrombosis. Conclusions: Val/Val genotype of β2-GPI gene is associated with a significant excess risk to suffer from APS and, among patients with APS, to have anti-β2-GPI antibodies. No definite conclusions can be made regarding the association of this polymorphism with thrombosis among APS patients. © 20
    URI
    https://hdl.handle.net/10366/154045
    ISSN
    1568-9972
    DOI
    10.1016/j.autrev.2011.12.006
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