Relationship between NF-κB1-94 ins/del ATTG polymorphism and susceptibility of multiple sclerosis in Iranian MS patients

被引:4
|
作者
Zahednasab, Hamid [1 ]
Mesbah-Namin, Seyed Alireza [1 ]
Sahraian, Mohammad Ali [2 ]
Balood, Mohammad [1 ]
Doosti, Rozita [2 ]
机构
[1] Tarbiat Modares Univ, Fac Med Sci, Dept Clin Biochem, Tehran, Iran
[2] Univ Tehran Med Sci, Brain & Spinal Injury Res Ctr, Siria MS Res Ctr, Tehran, Iran
关键词
Multiple sclerosis; NF-kappa B1; Polymorphism; NF-KAPPA-B; GENOME-WIDE ASSOCIATION; PROMOTER POLYMORPHISM; DIAGNOSTIC-CRITERIA; RISK; GUIDELINES;
D O I
10.1016/j.neulet.2013.04.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Multiple sclerosis (MS) is one of the most common neurological diseases of the central nervous system (CNS) which is mediated by the autoimmune reactions against myelin sheath. Both genetic and environmental factors are thought to be involved in the pathogenesis of MS. NF-kappa B1 is one of the most important molecules which regulates the immune functions. NF-kappa B1 -94 ins/del ATTG promoter polymorphism is a well-studied region in NF-kappa B1 gene associated with several common autoimmune diseases such as systemic lupus erythematosus (SLE). Our hypothesis was aimed to address the potential association of NF-kappa B polymorphism and MS. Therefore, we analyzed 200 sex and age matched MS patients along with 200 healthy individuals using PCR-RFLP. The data revealed no significant differences in the frequency of the -94 ins/del ATTG polymorphism in multiple sclerosis patients compared with the control group. To conclude, our study showed no association between -94 ins/del ATTG polymorphism and risk of multiple sclerosis in Iranian patients. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:46 / 49
页数:4
相关论文
共 47 条
  • [31] Correlation between heavy metal exposure and GSTM1 polymorphism in Iranian multiple sclerosis patients
    Aliomrani, Mehdi
    Sahraian, Mohammad A.
    Shirkhanloo, Hamid
    Sharifzadeh, Mohammad
    Khoshayand, Mohammad R.
    Ghahremani, Mohammad H.
    NEUROLOGICAL SCIENCES, 2017, 38 (07) : 1271 - 1278
  • [32] NF-κB1基因启动子-94ins/del ATTG的基因多态性与动脉粥样硬化性脑梗死的关系
    王锐
    张俊和
    陈立杰
    蒋殿飞
    中国神经免疫学和神经病学杂志, 2012, 19 (03) : 231 - 233+237
  • [33] NO ASSOCIATION OF THE NF-κB1-94INS/DELATTG PROMOTER POLYMORPHISM WITH RELAPSE-FREE AND OVERALL SURVIVAL IN PATIENTS WITH SQUAMOUS CELL CARCINOMAS OF THE HEAD AND NECK REGION
    Lehnerdt, G. F.
    Bankfalvi, A.
    Grehl, S.
    Adamzik, M.
    Lang, S.
    Schmid, K. W.
    Siffert, W.
    Riemann, K.
    INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 2008, 21 (04) : 827 - 832
  • [34] The NFKB1 Promoter Polymorphism (-94ins/delATTG) Alters Nuclear Translocation of NF-κB1 in Monocytes after Lipopolysaccharide Stimulation and Is Associated with Increased Mortality in Sepsis
    Adamzik, Michael
    Schaefer, Simon
    Frey, Ulrich H.
    Becker, Arne
    Kreuzer, Maximiliane
    Winning, Sandra
    Frede, Stilla
    Steinmann, Joerg
    Fandrey, Joachim
    Zacharowski, Kai
    Siffert, Winfried
    Peters, Juergen
    Hartmann, Matthias
    ANESTHESIOLOGY, 2013, 118 (01) : 123 - 133
  • [35] HLA class II (DRB1, DQA1 and DQB1) associated genetic susceptibility in Iranian multiple sclerosis (MS) patients
    Amirzargar, A
    Mytilineos, J
    Yousefipour, A
    Farjadian, S
    Scherer, S
    Opelz, G
    Ghaderi, A
    EUROPEAN JOURNAL OF IMMUNOGENETICS, 1998, 25 (04): : 297 - 301
  • [36] Relationship between HLA-DRB1 Genotype and Clinical Response to Interferon-Beta among Iranian Multiple Sclerosis Patients
    Samadzadeh, Sara
    Abolfazli, Roya
    Tabibian, Elnaz
    Shakoori, Abbas
    Sabokbar, Tayebeh
    Dehgolan, Shahram Rahimi
    MULTIPLE SCLEROSIS JOURNAL, 2016, 22 (03) : 412 - 412
  • [37] Relationship between HLA-DRB1 polymorphism and susceptibility or resistance to multiple sclerosis in Caucasians: A meta-analysis of non-family-based studies
    Zhang, Qiong
    Lin, Chun-Ying
    Dong, Qiang
    Wang, Jian
    Wang, Wei
    AUTOIMMUNITY REVIEWS, 2011, 10 (08) : 474 - 481
  • [38] The relationship between L-leucine-7-amido-4-methyl coumarin 1 gene polymorphism and susceptibility to the chronic hepatitis B virus infection in an Iranian population
    Moudi, Bite
    Heidari, Zahra
    Mahmoudzadeh-Sagheb, Hamidreza
    Farrokh, Parisa
    JOURNAL OF RESEARCH IN MEDICAL SCIENCES, 2018, 23
  • [39] Hydrocortisone Fails to Abolish NF-κB1 Protein Nuclear Translocation in Deletion Allele Carriers of the NFKB1 Promoter Polymorphism (-94ins/delATTG) and Is Associated with Increased 30-Day Mortality in Septic Shock
    Schaefer, Simon T.
    Gessner, Sophia
    Scherag, Andre
    Rump, Katharina
    Frey, Ulrich H.
    Siffert, Winfried
    Westendorf, Astrid M.
    Steinmann, Joerg
    Peters, Juergen
    Adamzik, Michael
    PLOS ONE, 2014, 9 (08):
  • [40] The SDF-1 3′A Genetic Variation of the Chemokine SDF-1α (CXCL12) in Parallel with its Increased Circulating Levels is Associated with Susceptibility to MS: A Study on Iranian Multiple Sclerosis Patients
    Azin, Hossein
    Vazirinejad, Reza
    Ahmadabadi, Behzad Nasiri
    Khorramdelazad, Hossein
    Zarandi, Ebrahim Rezazadeh
    Arababadi, Mohammad Kazemi
    Karimabad, Mojgan Noroozi
    Shamsizadeh, Ali
    Rafatpanah, Houshang
    Hassanshahi, Gholamhossein
    JOURNAL OF MOLECULAR NEUROSCIENCE, 2012, 47 (03) : 431 - 436