Previous studies reported an association with multiple sclerosis (MS) of distinct HLA-class I markers, namely HLA-A*02, HLA-Cw*05 and MOG-142L. In this work, we tested the association with MS of A*02 and Cw*05 in 1273 Italian MS patients and 1075 matched controls, which were previously analyzed for MOG-142, and explored the relationship among these three markers in modulating MS risk. HLA-A*02 conferred a statistically robust MS protection (odds ratio, OR=0.61; 95% confidence intervals, CI=0.51-0.72, P<10(-9)), which was independent of DRB1*15 and of any other DRB1* allele and remained similar after accounting for the other two analyzed class I markers. Conversely, the protective effect we previously observed for MOG-142L was secondary to its linkage disequilibrium with A*02. Cw*05 was not associated considering the whole sample, but its presence significantly enhanced the protection in the HLA-A*02-positive group, independently of DRB1: the OR conferred by A*02 in Cw*05-positive individuals (0.22, 95% CI=0.13-0.38) was significantly lower than in Cw*05-negative individuals (0.69, 95% CI=0.58-0.83) with a significant (P=4.94 x 10(-5)) multiplicative interaction between the two markers. In the absence of A*02, Cw*05 behaved as a risk factor, particularly in combination with DRB1*03 (OR=3.89, P=0.0006), indicating that Cw*05 might be a marker of protective or risk haplotypes, respectively.

HLA-class I markers and multiple sclerosis susceptibility in the Italian population / L., Bergamaschi; M. A., Leone; M. E., Fasano; F. R., Guerini; D., Ferrante; E., Bolognesi; N., Barizzone; L., Corrado; P., Naldi; C., Agliardi; E., Dametto; Salvetti, Marco; A., Visconti; D., Galimberti; E., Scarpini; M., Vercellino; R., Bergamaschi; F., Monaco; D., Caputo; P., Momigliano Richiardi; S., D'Alfonso. - In: GENES AND IMMUNITY. - ISSN 1466-4879. - 11:2(2010), pp. 173-180. [10.1038/gene.2009.101]

HLA-class I markers and multiple sclerosis susceptibility in the Italian population

SALVETTI, Marco;
2010

Abstract

Previous studies reported an association with multiple sclerosis (MS) of distinct HLA-class I markers, namely HLA-A*02, HLA-Cw*05 and MOG-142L. In this work, we tested the association with MS of A*02 and Cw*05 in 1273 Italian MS patients and 1075 matched controls, which were previously analyzed for MOG-142, and explored the relationship among these three markers in modulating MS risk. HLA-A*02 conferred a statistically robust MS protection (odds ratio, OR=0.61; 95% confidence intervals, CI=0.51-0.72, P<10(-9)), which was independent of DRB1*15 and of any other DRB1* allele and remained similar after accounting for the other two analyzed class I markers. Conversely, the protective effect we previously observed for MOG-142L was secondary to its linkage disequilibrium with A*02. Cw*05 was not associated considering the whole sample, but its presence significantly enhanced the protection in the HLA-A*02-positive group, independently of DRB1: the OR conferred by A*02 in Cw*05-positive individuals (0.22, 95% CI=0.13-0.38) was significantly lower than in Cw*05-negative individuals (0.69, 95% CI=0.58-0.83) with a significant (P=4.94 x 10(-5)) multiplicative interaction between the two markers. In the absence of A*02, Cw*05 behaved as a risk factor, particularly in combination with DRB1*03 (OR=3.89, P=0.0006), indicating that Cw*05 might be a marker of protective or risk haplotypes, respectively.
2010
myelin oligodendrocyte glycoprotein; hla-class i markers; genetic association; multiple sclerosis; extended hla haplotypes
01 Pubblicazione su rivista::01a Articolo in rivista
HLA-class I markers and multiple sclerosis susceptibility in the Italian population / L., Bergamaschi; M. A., Leone; M. E., Fasano; F. R., Guerini; D., Ferrante; E., Bolognesi; N., Barizzone; L., Corrado; P., Naldi; C., Agliardi; E., Dametto; Salvetti, Marco; A., Visconti; D., Galimberti; E., Scarpini; M., Vercellino; R., Bergamaschi; F., Monaco; D., Caputo; P., Momigliano Richiardi; S., D'Alfonso. - In: GENES AND IMMUNITY. - ISSN 1466-4879. - 11:2(2010), pp. 173-180. [10.1038/gene.2009.101]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/108445
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