Association Study between Functional Polymorphisms of MMP9 Gene Promoter and Multiple Sclerosis Susceptibility in an Iranian Population

Author(s):  
Sima SABBAGH ◽  
Zakiye NADEALI ◽  
Vahid SHAYGANNEJAD ◽  
Majid REZVANI ◽  
Masih SABOORI ◽  
...  

Background: Matrix metalloproteinase-9 (MMP-9) polymorphisms, C−1562 T and -90 (CA) n repeats, which influence transcriptional activity of this gene, are proposed to play a role in MS susceptibility and its development. In the present study, the possible association of MMP-9 polymorphisms in Iranian MS patients is studied. Methods: Association of MMP-9 mentioned gene polymorphisms with MS susceptibility was evaluated in unrelated Iranian subjects referred to Al-Zahra Hospital, Isfahan, Iran during 2014 to 2017. Results: -1562 T allele of MMP-9 was associated with increased MS risk. However, we found no overall significant effect of −90 (CA)n repeat on MS susceptibility. Conclusion: For as much as MMP-9 molecule is a potential target for MS therapy, to determine whether any of MMP-9 polymorphisms influence MS susceptibility in Iranian MS patients or not, concerning the significant influence of T allele on MS susceptibility and the non-significant association regarding CA repeats, further research is needed before proposing any definite conclusion.

2019 ◽  
Vol 55 (10) ◽  
pp. 1266-1272 ◽  
Author(s):  
N. Kh. S. Sadr ◽  
H. Galehdari ◽  
T. Seifi ◽  
N. Delfan ◽  
S. R. Khatami ◽  
...  

2008 ◽  
Vol 205 (1-2) ◽  
pp. 105-109 ◽  
Author(s):  
Yvonne Benešová ◽  
Anna Vašků ◽  
Pavel Štourač ◽  
Magdalena Hladíková ◽  
Michal Beránek ◽  
...  

2013 ◽  
Vol 48 (3) ◽  
pp. 255-256
Author(s):  
Ünsal Yılmaz ◽  
Kıvılcım Gücüyener ◽  
Esra Gürkaş ◽  
Ercan Demir ◽  
Ayşe Serdaroğlu ◽  
...  

2003 ◽  
Vol 9 (6) ◽  
pp. 535-539 ◽  
Author(s):  
Tineke Hooper-van Veen ◽  
Hans M Schrijver ◽  
Antoon Zwiers ◽  
J Bart A Crusius ◽  
Dirk L Knol ◽  
...  

Multiple sclerosis (MS) is a chronic disease of presumed autoimmune origin with a considerable polygenic influence. We have previously observed that a specific allele combination in genes of the interleukin-1 (IL-1) family influenced the progression rate in MS. We have considerably expanded our patient population (492 MS patients and 228 controls). In the present study, we investigated the role of the IL- 1A - 889, IL-1B - 511, IL-1B+3953 and IL-1RN VNTR gene polymorphisms in MS. In addition, we performed preliminary analyses on longitudinal magnetic resonance imaging (MRI) data. We found no associations between the polymorphisms and susceptibility to MS or clinical features. In addition, we observed no significant effect of the polymorphisms on brain or lesion volumes, Based on our data and those from the literature, one can conclude that there is currently no evidence to support a role for the IL-1 genes in MS.


2019 ◽  
Vol 21 (12) ◽  
Author(s):  
Mohsen Saravani ◽  
Mohsen Rokni ◽  
Mehrzad Mehrbani ◽  
Arian Amirkhosravi ◽  
Sanaz Faramarz ◽  
...  

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