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    DQB1*0602 allele shows a strong association with multiple sclerosis in patients in Malaga, Spain.

    • Autor
      Fernández-Fernández, Óscar; Fernández, Victoria; Alonso, Antonio; Caballero-González, AbelardoAutoridad Universidad de Málaga; Luque, Gloria; Bravo, Mariano; León-Martín, Antonio; Mayorga Mayorga, Cristobalina; Leyva-Fernández, LauraAutoridad Universidad de Málaga; De Ramón Garrido, Enrique
    • Fecha
      2004-04
    • Editorial/Editor
      Springer
    • Palabras clave
      Esclerosis múltiple; Mielina - Enfermedades - Aspectos genéticos
    • Resumen
      Background The human leukocyte antigen (HLA) class II DR2 haplotype (DRB1*1501, DQA1*0102, DQB1*0602) has been associated with multiple sclerosis (MS) in all ethnic groups and very strongly in Caucasians. Aim To investigate the possible HLA class II (DRB1,DQA1 and DQB1) associations with MS in Malaga, southern Spain. Methods We analysed the HLA class II sub-regions DRB1, DQA1 and DQB1 by polymerase chain reaction (PCR) and sequence-specific oligonucleotide probe hybridization (PCR/SSO) for DRB1 and DQB1 and with sequence-specific primers (PCR/SSP) for DRB1 subtypes and DQA1. Possible HLA class II associations with clinical MS characteristics were investigated in 149 subjects with and 160 without MS. Results Associations were detected between MS and the HLA class II alleles DRB1*1501 (45.6 % vs. 21.3%, p=0.001),DQA1*0102 (44% vs. 29.4%, p=0.001) and DQB1*0602 (45% vs. 20.6%, p=0.001). The DR2 haplotype (DRB1*1501, DQA1*0102, DQB1*0602) was associated with MS (43.6 % vs. 20%, p=0.002). DQB1*0602 was the only allele that maintained an association with MS in a logistic regression model. No HLA class II alleles or genotypes were significantly associated with any clinical characteristics of MS. Conclusions Our results confirm the positive association of the DR2 haplotype with MS, particularly the allele DQB1*0602, in the population studied. DR4 was not associated with the disease in Malaga. HLA class II alleles or haplotype were not associated with clinical or demographic characteristics, or clinical form or severity of MS.
    • URI
      https://hdl.handle.net/10630/32581
    • DOI
      https://dx.doi.org/10.1007/s00415-004-0350-2
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    Ficheros
    J Neurol (2004) vol 251, 440–444.pdf (794.9Kb)
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    REPOSITORIO INSTITUCIONAL UNIVERSIDAD DE MÁLAGA
    REPOSITORIO INSTITUCIONAL UNIVERSIDAD DE MÁLAGA
     

     

    REPOSITORIO INSTITUCIONAL UNIVERSIDAD DE MÁLAGA
    REPOSITORIO INSTITUCIONAL UNIVERSIDAD DE MÁLAGA