Alterations in KLRB1 gene expression and a Scandinavian multiple sclerosis association study of the KLRB1 SNP rs4763655

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Helle Bach Søndergaard
  • Sellebjerg, Finn Thorup
  • Jan Hillert
  • Tomas Olsson
  • Ingrid Kockum
  • Magdalena Lindén
  • Inger-Lise Mero
  • Kjell-Morten Myhr
  • Elisabeth G Celius
  • Hanne F Harbo
  • Jeppe Romme Christensen
  • Lars Börnsen
  • Sørensen, Per Soelberg
  • Annette Bang Oturai
Multiple sclerosis (MS) is a complex autoimmune disease affecting genetically susceptible individuals. A genome-wide association study performed by the International MS Genetics Consortium identified several putative susceptibility genes; among these, the KLRB1 gene is represented by the single-nucleotide polymorphism rs4763655. We could confirm a marginally significant association between rs4763655 and MS (P=0.046, odds ratio=1.06 (1.00-1.13)) in a large Scandinavian case-control study of 5367 MS patients and 4485 controls. The expression of KLRB1 in blood from MS patients was higher compared with healthy controls (P
OriginalsprogEngelsk
TidsskriftEuropean Journal of Human Genetics
Vol/bind19
Udgave nummer10
Sider (fra-til)1100-3
Antal sider4
ISSN1018-4813
DOI
StatusUdgivet - 2011

ID: 40194303