MGAT5 alters the severity of multiple sclerosis

J Neuroimmunol. 2010 Mar 30;220(1-2):120-4. doi: 10.1016/j.jneuroim.2010.01.003. Epub 2010 Feb 1.

Abstract

Multiple Sclerosis (MS) is a genetically complex immune mediated, demyelinating disease of the central nervous system. To date no genetic variants have been unambiguously linked to disease severity. We have conducted a genome wide screen, using Affymetrix Genechip 500K technology, for severity in 1040 MS patients. Two markers within MGAT5, a gene coding for a glycosylation enzyme, were found to be significantly associated with outcome in the screening as well as in an independent population (combined p-values: 2.8 x 10(-6) and 1.5 x 10(-7)).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cohort Studies
  • DNA Mutational Analysis
  • Disability Evaluation
  • Europe
  • Female
  • Genetic Markers / genetics
  • Genetic Predisposition to Disease / genetics*
  • Genetic Testing
  • Genetic Variation / genetics
  • Genome / genetics
  • Genome-Wide Association Study*
  • Genotype
  • Glycosylation
  • Humans
  • Male
  • Multiple Sclerosis / genetics*
  • Multiple Sclerosis / metabolism
  • Multiple Sclerosis / physiopathology
  • N-Acetylglucosaminyltransferases / genetics*
  • Nerve Tissue Proteins / genetics*
  • Oligonucleotide Array Sequence Analysis
  • Severity of Illness Index

Substances

  • Genetic Markers
  • Nerve Tissue Proteins
  • MGAT5B protein, human
  • N-Acetylglucosaminyltransferases