A Polymorphism Within the MBP Gene Is Associated With a Higher Relapse Number in Male Patients of Multiple Sclerosis

Myelin basic protein (MBP) is thought to be one of the key autoantigens in multiple sclerosis (MS) development. A recent study described the association of the single nucleotide polymorphism (SNP) rs12959006, within the gene, with a higher risk of relapse and worse prognosis. We aim at studying pote...

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Veröffentlicht in:Frontiers in immunology 2020-05, Vol.11, p.771-771
Hauptverfasser: Espino-Paisán, Laura, Agudo-Jiménez, Teresa, Rosales-Martínez, Isabel, López-Cotarelo, Pilar, García-Martínez, María Ángel, Domínguez-Mozo, María Inmaculada, Pérez-Pérez, Silvia, Dieli-Crimi, Romina, Comabella, Manuel, Urcelay, Elena, Álvarez-Lafuente, Roberto
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Sprache:eng
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Zusammenfassung:Myelin basic protein (MBP) is thought to be one of the key autoantigens in multiple sclerosis (MS) development. A recent study described the association of the single nucleotide polymorphism (SNP) rs12959006, within the gene, with a higher risk of relapse and worse prognosis. We aim at studying potential associations of this SNP to MS in an independent population. Clinical data of the first 5 years of the disease were collected retrospectively from 291 MS confirmed patients. polymorphism rs12959006 was genotyped in all patients. Associations with EDSS, number of relapses and serology for Herpesvirus 6 (HHV-6) and Epstein Barr (EBV) viruses were studied. Lymphocyte activation measured by CD69 expression was also analyzed according to sex and rs12959006 genotype. The rs12959006 polymorphism contributed significantly to a higher number of relapses at 5 years after onset only in male patients (rs12959006 TT β = 0.74 [0.36-1.09]; = 7 × 10 ). Titers of anti-HHV6 IgG antibodies showed also a mild association with relapses, both in male and female patients (β = 0.01 [0.01-0.02]; = 3.7 × 10 ). Both the genetic variation in and HHV-6 infection aid in predicting a higher number of relapses during the first years of MS. The association described in rs12959006 T is exclusive to male patients.
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2020.00771