Matrix metalloproteinase-9-1562 C/T gene polymorphism in Serbian patients with multiple sclerosis
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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 NIS 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. (C) 2007 Elsevier B.V. All rights reserved.
Кључне речи:MMP-9 / gene / polymorphism / multiple sclerosis
Извор:Journal of Neuroimmunology, 2007, 189, 1-2, 147-150
ISSN: 0165-5728 (print)