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PDE4D 和 IL-1 基因多态性与汉族人群缺血性脑卒中的关联。

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

机构信息

Department of Neurology, The First Affiliated Hospital of China Medical University, Shenyang 110001, China.

出版信息

Brain Res Bull. 2010 Jan 15;81(1):38-42. doi: 10.1016/j.brainresbull.2009.09.009.

Abstract

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.

摘要

背景

磷酸二酯酶 4D(PDE4D)和白细胞介素-1(IL-1)基因的单核苷酸多态性(SNP)与白人缺血性中风(IS)的发病风险增加相关。然而,目前尚不清楚这种关联是否也可能发生在汉族人群中。

方法

共招募了 371 例 IS 患者和无关的健康对照者,分别通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析 PDE4D(83T/C)、(87T/C)、IL-1(-889C/T)和 IL-1(-511C/T)的 SNP。对该人群中这些 SNP 的基因型和等位基因频率进行了统计学分析。

结果

IS 患者与对照组的 PDE4D(87T/C)和 IL-1(-511C/T)基因型和等位基因频率相似。相比之下,PDE4D(83T/C)的 CC 基因型和 C 等位基因以及 IL-1(-889C/T)的 T 等位基因频率在 IS 患者中显著高于健康对照组(p=0.001,p=0.003 和 p=0.02),独立于传统的危险因素。PDE4D(83T/C)的 CC 基因型的比值比(OR)达到 1.603;95%CI=1.032-2.489;p=0.036,IL-1(-889C/T)的 TT 基因型的 OR 为 1.913;95%CI=1.621-2.375;p=0.034。

结论

PDE4D(83T/C)和 IL-1(-889C/T)的 SNP 与北方汉族人群 IS 的发病风险增加相关。

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