Analysis of polymorphisms in RIG-I-like receptor genes in German multiple sclerosis patients

Alexander Varzari, Kathrin Bruch, Igor V. Deyneko, Andrew Chan, Joerg T. Epplen, Sabine Hoffjan

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Variation in genes encoding retinoid acid-inducible gene I (RIG-I)-like receptors (RLRs) has been implicated in the pathogenesis of autoimmune disorders. We investigated if polymorphisms in the IFIH1, RIG-. I, LGP2 and VISA genes influence the risk for multiple sclerosis (MS) in a German case-control cohort comprising 716 patients and 706 controls. Evaluation of 18 single nucleotide polymorphisms (SNPs) in the four genes did not reveal significant single-SNP associations with MS risk, but two VISA polymorphisms were modestly associated with age of onset. Further, we provide initial evidence for combinatorial effects of polymorphic variants in the RIG-. I, LGP2 and IFIH1 genes on MS risk.

Original languageEnglish
Pages (from-to)140-144
Number of pages5
JournalJournal of Neuroimmunology
Volume277
Issue number1-2
DOIs
StatePublished - 15 Dec 2014
Externally publishedYes

Keywords

  • Association
  • Combinatorial effect
  • Multiple sclerosis
  • RIG-I-like receptors
  • RLRs

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