4.5 Article

The role of HLA-DRB1 alleles on susceptibility and outcome of a Portuguese Multiple Sclerosis population

Journal

JOURNAL OF THE NEUROLOGICAL SCIENCES
Volume 258, Issue 1-2, Pages 69-74

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jns.2007.02.033

Keywords

multiple sclerosis; HLA; Portugal; DRB1*15; class II

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Background: The association between susceptibility to multiple sclerosis (MS) and HLA-DRB1*15 has been reported in various European populations. Objective: To investigate the relationship between MS, HLA-DRB1*15 and other DRB1 alleles in a Portuguese population and their association with clinical course of MS. Methods: The HLA-DRB1 alleles were analyzed by PCR-SSP in 248 MS patients and 282 healthy controls. In order to relate HLA-DRB1 alleles to disease aggressiveness, patients with relapsing remitting MS and secondary progressive MS were subdivided into 3 groups: 'benign' MS patients who maintain an Extended Disability Status Scale (EDSS) score of : 3 at least 10 years after disease onset; non-benign MS patients with EDSS > 3 after the same period and 'aggressive' MS those with EDSS = 6 within 15 years of disease onset. Results: As expected, a higher frequency of HLA-DRB1*15 was found in MS patients (29.8% vs 19.9%, odds ratio (OR) = 1.72, 95% CI= 1.15-2.56, p = 0.008). The HLA-DRB1*03 allele was positively associated with MS in the overall patient population (22.6% vs 15.6%, OR= 1.58,95% CI= 1.022.45). Concerning disease aggressiveness, HLA-DRB1*15 occurred more frequently in the group with benign disease (42.6% vs 19.9%, OR= 2.99, 95% CI = 1.56-5.72) and in the group with non-benign disease (34.1 % vs 19.9%, OR= 2.09, 95% CI = 1.05-4.16) compared with controls. When time to reach an EDSS = 3 or EDSS = 6 was considered as end point, HLA-DRB1*15 negative patients were found to have a worse prognosis. Conclusions: In this population of Portuguese MS patients, the HLA-DRB1*15 allele is established as a genetic marker for susceptibility to MS and is also associated with a better outcome. (c) 2007 Elsevier B.V All rights reserved.

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