Interleukin-18 promoter polymorphisms and risk of ischemic stroke

被引:31
作者
Zhang, Na [1 ]
Yu, Jin-Tai [1 ]
Yu, Nan-Nan [1 ]
Lu, Rui-Chun [1 ]
Ma, Teng [2 ]
Wang, Nai-Dong [3 ]
Miao, Dan [1 ]
Song, Jing-Hui [3 ]
Tan, Lan [1 ]
机构
[1] Qingdao Univ, Dept Neurol, Qingdao Municipal Hosp, Sch Med, Qingdao 266071, Shandong, Peoples R China
[2] Qingdao Hiser Hosp, Dept Neurol, Qingdao, Shandong, Peoples R China
[3] Qingdao Univ, Affiliated Hosp, Coll Med, Dept Neurol, Qingdao, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Ischemic stroke; Inflammation; Interleukin-18; Polymorphisms; HUMAN ATHEROSCLEROTIC PLAQUES; RHEUMATOID-ARTHRITIS PATIENTS; NECROSIS-FACTOR-ALPHA; MYOCARDIAL-INFARCTION; GENE POLYMORPHISMS; CORONARY-ARTERY; ATRIAL-FIBRILLATION; INTERFERON-GAMMA; ASSOCIATION; CYTOKINE;
D O I
10.1016/j.brainresbull.2010.01.008
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Ischemic stroke (IS) is a major cause of morbidity and mortality around the world. Interleukin-18 (IL-18) plays an important role in the pathogenesis of IS and IL-18 promoter polymorphisms have been shown to be associated with levels of expression of IL-18. We investigated the association of two functional polymorphisms in IL-18 promoter, -607C/A (rs1946518) and -137G/C (rs187238), with the risk of ischemic stroke in a Han Chinese population of 423 patients and 384 healthy controls matched for sex and age. The results revealed that the -607C allele was associated with an increased risk of IS with an odds ratios (OR) of 1.358 (P = 0.002, power = 100%) and the presence of the -137G allele was correlated with increased the risk of IS in the subtype of patients with large artery atherosclerosis (LAA)(OR = 1.583, P = 0.02, power = 94%). Patients with the -607C/-137G haplotype also had significantly increased risk of IS compared to controls (CR = 1.341, P = 0.005, power = 100%). Our findings suggest that these functional polymorphisms in the IL-18 promoter are involved in development of IS in the Han Chinese population. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:590 / 594
页数:5
相关论文
共 57 条
[1]
IL-18 gene polymorphisms affect IL-18 production capability by monocytes [J].
Arimitsu, J ;
Hirano, T ;
Higa, S ;
Kawal, M ;
Naka, T ;
Ogata, A ;
Shima, Y ;
Fujimoto, M ;
Yamadori, T ;
Hagiwara, K ;
Ohgawara, T ;
Kuwabara, Y ;
Kawase, I ;
Tanaka, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 342 (04) :1413-1416
[2]
Interleukin-18 gene polymorphisms and haplotypes in patients with oral lichen planus: a study in an ethnic Chinese cohort [J].
Bai, J. ;
Zhang, Y. ;
Lin, M. ;
Zeng, X. ;
Wang, Z. ;
Shen, J. ;
Jiang, L. ;
Gao, F. ;
Chen, Q. .
TISSUE ANTIGENS, 2007, 70 (05) :390-397
[3]
The IL-6 G-174C polymorphism may be associated with ischaemic stroke in patients without a history of hypertension [J].
Balding, J ;
Livingstone, WJ ;
Pittock, SJ ;
Mynett-Johnson, L ;
Ahern, T ;
Hodgson, A ;
Smith, OP .
IRISH JOURNAL OF MEDICAL SCIENCE, 2004, 173 (04) :200-203
[4]
Inflammatory system gene polymorphism and the risk of stroke: A case-control study in an Indian population [J].
Banerjee, Indranil ;
Gupta, Veena ;
Ahmed, Tanveer ;
Faizaan, Mohammad ;
Agarwal, Puneet ;
Ganesh, Subramaniam .
BRAIN RESEARCH BULLETIN, 2008, 75 (01) :158-165
[5]
Variation in inflammation-related genes and risk of incident nonfatal myocardial infarction or ischemic stroke [J].
Bis, Joshua C. ;
Heckbert, Susan R. ;
Smith, Nicholas L. ;
Reiner, Alexander P. ;
Rice, Kenneth ;
Lumley, Thomas ;
Hindorff, Lucia A. ;
Marciante, Kristin D. ;
Enquobahrie, Daniel A. ;
Monks, Stephanie A. ;
Psaty, Bruce M. .
ATHEROSCLEROSIS, 2008, 198 (01) :166-173
[6]
Interleukin 18 gene polymorphisms predict risk and outcome of Alzheimer's disease [J].
Bossu, Paola ;
Ciaramella, Antonio ;
Moro, Maria Luisa ;
Bellincampi, Lorenza ;
Bernardini, Sergio ;
Federici, Giorgio ;
Trequattrini, Alberto ;
Macciardi, Fabio ;
Spoletini, Ilaria ;
Di Iulio, Fulvia ;
Caltagirone, Carlo ;
Spalletta, Gianfranco .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2007, 78 (08) :807-811
[7]
The pro-atherogenic cytokine interleukin-18 induces CXCL16 expression in rat aortic smooth muscle cells via MyD88, interleukin-1 receptor-associated kinase, tumor necrosis factor receptor-associated factor 6, c-Src, phosphatidylinositol 3-kinase, Akt, c-Jun N-terminal kinase, and activator protein-1 signaling [J].
Chandrasekar, B ;
Mummidi, S ;
Valente, AJ ;
Patel, DN ;
Bailey, SR ;
Freeman, GL ;
Hatano, M ;
Tokuhisa, T ;
Jensen, LE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (28) :26263-26277
[8]
Interferon-gamma-inducing factor, a novel cytokine, enhances Fas ligand-mediated cytotoxicity of murine T helper 1 cells [J].
Dao, T ;
Ohashi, K ;
Kayano, T ;
Kurimoto, M ;
Okamura, H .
CELLULAR IMMUNOLOGY, 1996, 173 (02) :230-235
[9]
Dinarello CA, 2002, CLIN EXP RHEUMATOL, V20, pS1
[10]
Arlequin (version 3.0): An integrated software package for population genetics data analysis [J].
Excoffier, Laurent ;
Laval, Guillaume ;
Schneider, Stefan .
EVOLUTIONARY BIOINFORMATICS, 2005, 1 :47-50