Association of PDE4D and IL-1 gene polymorphism with ischemic stroke in a Han Chinese population

被引:44
|
作者
Li, Nan [1 ]
He, Zhiyi [1 ]
Xu, Jialiang [1 ]
Liu, Fang [1 ]
Deng, Shumin [1 ]
Zhang, Hui [1 ]
机构
[1] China Med Univ, Dept Neurol, Affiliated Hosp 1, Shenyang 110001, Peoples R China
关键词
Inflammation; Polymorphism; PDE4D; IL-1; Association; Ischemic stroke; PHOSPHODIESTERASE 4D GENE; FOLLOW-UP; RISK; ATHEROSCLEROSIS; DISEASE; MECHANISMS; HISTORY; TWINS;
D O I
10.1016/j.brainresbull.2009.09.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: The single-nucleotide polymorphisms (SNPs) of the phosphodiesterase 4D (PDE4D) and interleukin-1 (IL-1) genes are associated with increased risk for the development of ischemic stroke (IS) in whites. However, little is known about whether this association could also occur in Han Chinese. Method: A total of 371 patients with IS and unrelated healthy controls were recruited and the SNPs of the PDE4D (83T/C), (87T/C), IL-1 (-889C/T) and IL-1 (-511C/T) were characterized, respectively, by polymerase chain reactions-restriction fragment length polymorphism (PCR-RFLP). The genotype and allele frequencies of these SNPs in this population were statistically analyzed. Results: The genotype and allele frequencies of the PDE4D (87T/C) and IL-1 (-511C/T) were similar between IS patients and controls. In contrast, the frequencies of CC genotype and C allele of the PDE4D (83T/C) and the T allele frequency of IL-1 (-889C/T) in IS patients were significantly higher than that in healthy controls (p=0.001, p=0.003 and p=0.02, respectively), independent of the conventional risk factors. The values of odds ratio (OR) reached at OR=1.603; 95%CI=1.032-2.489; p=0.036 for the CC genotype of the PDE4D (83T/C) and OR=1.913; 95%CI=1.621-2.375; p=0.034 for the TT genotype of the IL-1 (-889C/T), respectively. Conclusions: the SNPs of the PDE4D (83T/C) and IL-1 (-889C/T) were associated with increased risk for the development of IS in Northern Han Chinese. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:38 / 42
页数:5
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