No support for a truncated interferon-alpha 17 allele as risk factor for MS.

Abstract:

:Cytokines have a central role in multiple sclerosis (MS) pathogenesis and may contribute to the aetiology of MS. A polymorphism in the IFNA17 gene with an allele carrying a pre-mature stop codon has been suggested to convey a 26-fold increased risk for MS. We investigated the possible association between this polymorphism and MS using population-based samples from a genetically well-characterized population. The IFNA17 gene variant was found in 2.8% of 327 MS cases and 3.3% of 698 referents (P = 0.64). Thus, our study does not support an association between the IFNA17 allele and risk for MS.

journal_name

Eur J Neurol

authors

Nyström M,Ruuth K,Lundgren E,Sundström P

doi

10.1111/j.1468-1331.2007.01953.x

subject

Has Abstract

pub_date

2007-11-01 00:00:00

pages

1302-4

issue

11

eissn

1351-5101

issn

1468-1331

pii

ENE1953

journal_volume

14

pub_type

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