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Eur J Neurol ; 18(10): 1258-62, 2011 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-21418440

RESUMEN

BACKGROUND AND OBJECTIVE: The HLA-DRB1*15 allele is consistently associated with multiple sclerosis (MS) susceptibility in most studied populations. This study investigated the association between HLA-DRB1 alleles and the presence of oligoclonal immunoglobulin G bands (OCB) in the cerebrospinal fluid (CSF) in a Spanish population with MS. METHODS: The HLA-DRB1 typing was performed in 268 patients with sporadic MS and the detection of OCB in CSF. HLA-DRB1 allelic frequencies were compared between OCB-positive and OCB-negative patients, and both groups were also compared with 1088 unrelated healthy controls. Moreover, we correlated the various HLA-DRB1 genotypes, considering all the combinations of both parental alleles found with the presence or absence of OCB. RESULTS: We found 206 OCB-positive and 62 OCB-negative patients. The HLA-DRB1*15 allele in OCB-positive patients had a higher frequency when compared with OCB-negative patients (39.3% in OCB-positive vs. 16.1% in OCB-negative, OR = 1.38 95% CI = 1.18-1.61, P < 0.001). The other alleles did not show differences. When we compared with controls, the HLA-DRB1*15 allele was associated with the disease only in the OCB-positive patients group. None of the 55 genotypes found showed any association with the presence or absence of OCB. CONCLUSIONS: HLA-DRB1*15 allele is associated with OCB-positive patients with MS when studying a Spanish MS population.


Asunto(s)
Predisposición Genética a la Enfermedad/genética , Cadenas HLA-DRB1/genética , Esclerosis Múltiple/epidemiología , Esclerosis Múltiple/genética , Bandas Oligoclonales/genética , Polimorfismo Genético/genética , Adulto , Alelos , Estudios de Cohortes , Femenino , Predisposición Genética a la Enfermedad/epidemiología , Cadenas HLA-DRB1/inmunología , Humanos , Inmunoglobulina G/líquido cefalorraquídeo , Inmunoglobulina G/genética , Masculino , Esclerosis Múltiple/inmunología , Bandas Oligoclonales/líquido cefalorraquídeo , Polimorfismo Genético/inmunología , Prevalencia , España/epidemiología
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