Matrix metalloproteinase-9 genotypes and haplotypes are associated with multiple sclerosis and with the degree of disability of the disease

J Neuroimmunol. 2009 Sep 29;214(1-2):128-31. doi: 10.1016/j.jneuroim.2009.07.004. Epub 2009 Jul 24.

Abstract

Multiple sclerosis (MS) is an autoimmune disease causing severe neurological disability. This study was carried out in order to determine whether the MMP-9 C(-1562)T and (CA)(13-25) polymorphisms are associated with MS. A total of 165 patients (92 whites/73 mulattos) and 191 controls (96 whites/95 mulattos) were enrolled in the study. While no difference in C(-1562)T polymorphism was observed between MS and healthy subjects, (CA)(n) genotypes and alleles were associated with MS. Moreover, the haplotypes are not associated with MS but seem to be relevant to the clinical status of MS. Thus the (CA)(n) polymorphism may contribute to MS susceptibility, but C(-1562)T and (CA)(n) haplotypes may modulate disease severity.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Brazil / epidemiology
  • Case-Control Studies
  • Disability Evaluation*
  • Disabled Persons*
  • Female
  • Genetic Predisposition to Disease
  • Genotype
  • Haplotypes
  • Humans
  • Male
  • Matrix Metalloproteinase 9 / genetics*
  • Middle Aged
  • Multiple Sclerosis / enzymology
  • Multiple Sclerosis / ethnology
  • Multiple Sclerosis / genetics*
  • Polymorphism, Single Nucleotide*
  • Severity of Illness Index

Substances

  • Matrix Metalloproteinase 9