Osteopontin polymorphisms and disease course in multiple sclerosis.

Journal Article

Osteopontin (OPN), also known as early T-cell activating gene (Eta-1), has been recently shown to be a critical factor in the progression of experimental autoimmune encephalomyelitis, and perhaps multiple sclerosis (MS). Here we investigated whether the 327T/C, 795C/T, 1128A/G or 1284A/C single-nucleotide polymorphisms in the OPN gene were correlated with susceptibility or any of the several clinical end points in a cohort of 821 MS patients. Overall, we observed no evidence of genetic association between the OPN polymorphisms and MS. Although not reaching statistical significance, a modest trend for association with disease course was detected in patients carrying at least one wild-type 1284A allele, suggesting an effect on disease course. Patients with this genotype were less likely to have a mild disease course and were at increased risk for a secondary-progressive clinical type.

Full Text

Duke Authors

Cited Authors

  • Caillier, S; Barcellos, LF; Baranzini, SE; Swerdlin, A; Lincoln, RR; Steinman, L; Martin, E; Haines, JL; Pericak-Vance, M; Hauser, SL; Oksenberg, JR; Multiple Sclerosis Genetics Group,

Published Date

  • June 2003

Published In

Volume / Issue

  • 4 / 4

Start / End Page

  • 312 - 315

PubMed ID

  • 12761568

International Standard Serial Number (ISSN)

  • 1466-4879

Digital Object Identifier (DOI)

  • 10.1038/sj.gene.6363952

Language

  • eng

Conference Location

  • England