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Related Experiment Video

Updated: Jul 6, 2026

Induction and Diverse Assessment Indicators of Experimental Autoimmune Encephalomyelitis
06:19

Induction and Diverse Assessment Indicators of Experimental Autoimmune Encephalomyelitis

Published on: September 9, 2022

EVI5 is a risk gene for multiple sclerosis.

I A Hoppenbrouwers1, Y S Aulchenko, G C Ebers

  • 1Department of Neurology, MS Centre ErasMS, Erasmus MC, Rotterdam, The Netherlands.

Genes and Immunity
|April 11, 2008
PubMed
Summary
This summary is machine-generated.

This study identifies the EVI5 gene as a novel risk locus for multiple sclerosis (MS). Further research is needed to uncover the complete genetic basis of MS.

Related Experiment Videos

Last Updated: Jul 6, 2026

Induction and Diverse Assessment Indicators of Experimental Autoimmune Encephalomyelitis
06:19

Induction and Diverse Assessment Indicators of Experimental Autoimmune Encephalomyelitis

Published on: September 9, 2022

Area of Science:

  • Genetics
  • Immunology
  • Neurology

Background:

  • The human leukocyte antigen (HLA)-DRB1 locus is a primary genetic risk factor for multiple sclerosis (MS).
  • Previous genome-wide studies identified single-nucleotide polymorphisms (SNPs) in IL2RA and IL7RA associated with MS risk.
  • Thirteen additional SNPs showed consistent but less significant associations with MS.

Purpose of the Study:

  • To verify the association of previously identified SNPs with MS in a Dutch genetically isolated population.
  • To identify novel genetic risk factors for MS.

Main Methods:

  • Genotyping of SNPs in 46 MS patients and 194 controls from a Dutch population.
  • Replication analysis in an independent cohort of 1318 MS patients (Canadian Collaborative Project on the Genetic Susceptibility to MS).
  • Transmission disequilibrium testing (TDT) was employed for risk effect validation.

Main Results:

  • The EVI5 gene on chromosome 1 was confirmed as a novel MS risk gene, exhibiting higher odds ratios (ORs 2.01 and 1.9; P=0.01) than previously reported.
  • The risk effect of EVI5 was validated in a larger MS cohort, showing a weak but significant association (OR 1.15; P=0.03 and OR 1.15; P=0.04) via TDT.
  • Apart from the HLA locus, EVI5 emerged as a significant genetic risk factor for MS.

Conclusions:

  • EVI5 is confirmed as a novel genetic risk locus for multiple sclerosis.
  • Despite identifying EVI5, a substantial portion of the genetic underpinnings of MS remains to be elucidated.
  • Further genetic studies are warranted to fully understand MS susceptibility.