Paraoxonase 1 activity and polymorphisms in multiple sclerosis patients

被引:0
|
作者
Monika Ďurfinová
Radka Bartová
L’ubica Procházková
Darina Petrleni čová
Pavel Sýkora
Vanda Repiská
机构
[1] Comenius University,Institute of Medical Chemistry, Biochemistry and Clinical Biochemistry, Faculty of Medicine
[2] Comenius University,2nd Department of Neurology, Faculty of Medicine
[3] Department of Surgery,Institute of Medical Biology, Genetic and Clinical Genetics, Faculty of Medicine
[4] Comenius University,undefined
来源
Biologia | 2015年 / 70卷
关键词
paraoxonase; genetic polymorphism; multiple sclerosis;
D O I
暂无
中图分类号
学科分类号
摘要
The pathophysiology of multiple sclerosis (MS) includes also the vascular abnormalities. Recent reports on changes in venous cerebrospinal outflow and the investigation of immunomodulatory properties of several vascular mediators on the molecular level have added new information to hypotheses on vascular pathology as determining factor in the pathophysiology of MS. We assessed changes in serum paraoxonase 1 (PON1) activities in MS patients and polymorphism of PON1 as a risk factor for MS. The main role of serum PON1 is hydrolysis of lipid peroxides and protection of low-density lipoprotein particles from oxidation. These events could play a role in lowering the risk of atherogenesis and vascular complications development in MS. There are controversial results about association of two main polymorphisms in paraoxonase coding region (PON1 55L/M, PON1 192Q/R) and risk of MS in different populations. Our results support studies that PON1 polymorphisms are probably not a risk factor of MS development.
引用
收藏
页码:1672 / 1676
页数:4
相关论文
共 50 条
  • [31] RAGE Gene Polymorphisms in Patients with Multiple Sclerosis
    Zoltán Tiszlavicz
    Zsofia Gyulai
    Krisztina Bencsik
    Zoltán Szolnoki
    Ágnes Katalin Kocsis
    Ferenc Somogyvári
    László Vécsei
    Yvette Mándi
    Journal of Molecular Neuroscience, 2009, 39 : 360 - 365
  • [32] RAGE Gene Polymorphisms in Patients with Multiple Sclerosis
    Tiszlavicz, Zoltan
    Gyulai, Zsofia
    Bencsik, Krisztina
    Szolnoki, Zoltan
    Kocsis, Agnes Katalin
    Somogyvari, Ferenc
    Vecsei, Laszlo
    Mandi, Yvette
    JOURNAL OF MOLECULAR NEUROSCIENCE, 2009, 39 (03) : 360 - 365
  • [33] Paraoxonase1 (An Antioxidant): A Marker of Treatment Response in Multiple Sclerosis?
    Csepany, Tunde
    Racz, Lilla
    Padra, Janos
    Mezei, Zsolt
    Csiba, Laszlo
    Paragh, Gyorgy
    Seres, Ildiko
    NEUROLOGY, 2013, 80
  • [34] Genetic analysis of SLC11A1 polymorphisms in multiple sclerosis patients
    Comabella, M
    Altet, L
    Peris, F
    Villoslada, P
    Sánchez, A
    Montalban, X
    MULTIPLE SCLEROSIS JOURNAL, 2004, 10 (06) : 618 - 620
  • [35] CTLA4 exon 1 and promoter polymorphisms in patients with multiple sclerosis
    Yousefipour, G.
    Erfani, N.
    Momtahan, M.
    Moghaddasi, H.
    Ghaderi, A.
    ACTA NEUROLOGICA SCANDINAVICA, 2009, 120 (06): : 424 - 429
  • [36] Paraoxonase 1 Activity and Survival in Sepsis Patients
    Inal, Volkan
    Yamanel, Levent
    Taskin, Gurhan
    Tapan, Serkan
    Comert, Bilgin
    BALKAN MEDICAL JOURNAL, 2015, 32 (02) : 183 - 188
  • [37] Paraoxonase 1 activity does not change in stable and progressive type of multiple sclerosis but decreases during relapse of the disease
    Jamroz-Wisniewska, A.
    Bartosik-Psujek, H.
    Beltowski, J.
    Stelmasiak, Z.
    JOURNAL OF NEUROLOGY, 2008, 255 : 141 - 142
  • [38] DRA promoter polymorphisms in Australian multiple sclerosis patients
    Bennetts, B
    Teutsch, S
    Stewart, G
    HUMAN IMMUNOLOGY, 1996, 47 (1-2) : O145 - O145
  • [39] Polymorphisms of apolipoprotein E and Japanese patients with multiple sclerosis
    Niino, M
    Kikuchi, S
    Fukazawa, T
    Yabe, I
    Tashiro, K
    MULTIPLE SCLEROSIS JOURNAL, 2003, 9 (04) : 382 - 386
  • [40] GENETIC POLYMORPHISMS OF HUMAN β-DEFENSINS IN PATIENTS WITH MULTIPLE SCLEROSIS
    Szekeres, Marta
    Somogyvari, Ferenc
    Bencsik, Krisztina
    Szolnoki, Zoltan
    Vecsei, Laszlo
    Mandi, Yvette
    IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE, 2015, 68 (3-4): : 127 - 133