Matrix metalloproteinase-9 -1562 C/T gene polymorphism in Serbian patients with multiple sclerosis

J Neuroimmunol. 2007 Sep;189(1-2):147-50. doi: 10.1016/j.jneuroim.2007.06.022. Epub 2007 Jul 25.

Abstract

Matrix metalloproteinase-9 (MMP-9) is suggested to play a role in MS by mediating T cell migration across subendothelial basement membrane and by contribution to myelin breakdown. We studied the association of MMP-9 -1562 C/T gene polymorphisms with MS susceptibility and severity in 187 patients from Serbia. The significant decrease in T allele carriership (p = 0.01), was found in female MS patients. In addition, a trend toward lower MSSS in T allele carriers was noticed (CC, mean 5.7 +/- 2.5 vs. CT+TT, mean 4.9 +/- 2.5). Further studies in different populations are needed to resolve the potential influence of MMP-9 gene polymorphism on MS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alleles
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease*
  • Humans
  • Male
  • Matrix Metalloproteinase 9 / genetics*
  • Middle Aged
  • Multiple Sclerosis / genetics*
  • Polymorphism, Single Nucleotide / genetics*
  • Severity of Illness Index
  • Sex Factors
  • Statistics, Nonparametric
  • Yugoslavia / epidemiology

Substances

  • Matrix Metalloproteinase 9