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 language | English |
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Pages (from-to) | 140-144 |
Number of pages | 5 |
Journal | Journal of Neuroimmunology |
Volume | 277 |
Issue number | 1-2 |
DOIs | |
State | Published - 15 Dec 2014 |
Externally published | Yes |
Keywords
- Association
- Combinatorial effect
- Multiple sclerosis
- RIG-I-like receptors
- RLRs