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炎症系统基因多态性与中风风险:一项针对印度人群的病例对照研究。

Inflammatory system gene polymorphism and the risk of stroke: a case-control study in an Indian population.

作者信息

Banerjee Indranil, Gupta Veena, Ahmed Tanveer, Faizaan Mohammad, Agarwal Puneet, Ganesh Subramaniam

机构信息

Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur 208016, India.

出版信息

Brain Res Bull. 2008 Jan 31;75(1):158-65. doi: 10.1016/j.brainresbull.2007.08.007. Epub 2007 Sep 24.

Abstract

Sequence variations in genes involved in inflammation system are known to contribute to the risk of cardiovascular diseases (CVD) including stroke. In this study, we performed a genetic association study on the single nucleotide polymorphisms (SNPs) present in the genes CD14 (-159 C/T), TNFalpha (-308 G/A), IL-1alpha (-889 C/T), IL-6 (-174 G/C), PSMA6 (-8 C/G), and PDE4D (SNP83 T/C, respectively) in order to discern their possible role in the susceptibility to stroke in a North Indian population. These SNPs were previously found to be associated with CVD through their contribution to inflammation. A case-control design was used to examine 176 stroke patients (112 ischemic and 64 hemorrhagic stroke patients) and 212 unrelated healthy control individuals. After adjustment for the confounding risk factors, the IL-1alpha -889 T allele carriers (TT+CT) were found to be strongly associated with both forms of stroke (OR=2.56; 95% CI=1.53-4.29; P=0.0004). The CC genotype of PDE4D was found to be associated only with ischemic stroke (OR=2.02; 95% CI=1.08-3.76; P=0.03). None of the variants tested for the CD14, TNFalpha, IL-6, and PSMA6 genes found to confer risk for stroke in the study population. In conclusion, the -889 C/T and SNP83 T/C SNPs of the IL-1alpha and PDE4D genes, respectively, appear to be genetic risk factors for stroke in our study population.

摘要

已知炎症系统相关基因的序列变异会增加包括中风在内的心血管疾病(CVD)风险。在本研究中,我们对CD14(-159 C/T)、TNFα(-308 G/A)、IL-1α(-889 C/T)、IL-6(-174 G/C)、PSMA6(-8 C/G)和PDE4D(分别为SNP83 T/C)基因中的单核苷酸多态性(SNP)进行了基因关联研究,以确定它们在北印度人群中风易感性中的可能作用。此前发现这些SNP通过对炎症的影响与CVD相关。采用病例对照设计,研究了176例中风患者(112例缺血性中风和64例出血性中风患者)和212名无亲缘关系的健康对照个体。在对混杂风险因素进行校正后,发现IL-1α -889 T等位基因携带者(TT+CT)与两种类型的中风均密切相关(OR=2.56;95%CI=1.53-4.29;P=0.0004)。发现PDE4D的CC基因型仅与缺血性中风相关(OR=2.02;95%CI=1.08-3.76;P=0.03)。在研究人群中,未发现CD14、TNFα、IL-6和PSMA6基因检测的任何变异会增加中风风险。总之,在我们的研究人群中,IL-1α基因的-889 C/T和PDE4D基因的SNP83 T/C SNP似乎是中风的遗传风险因素。

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