Suppr超能文献

炎症基因多态性与汉族人群缺血性脑卒中的相关性研究。

Association of inflammatory gene polymorphisms with ischemic stroke in a Chinese Han population.

机构信息

Department of Epidemiology, Public Health School, Harbin Medical University, Heilongjiang, China.

出版信息

J Neuroinflammation. 2012 Jul 6;9:162. doi: 10.1186/1742-2094-9-162.

Abstract

BACKGROUND

Inflammatory mechanisms are important in stroke risk, and genetic variations in components of the inflammatory response have been implicated as risk factors for stroke. We tested the inflammatory gene polymorphisms and their association with ischemic stroke in a Chinese Han population.

METHODS

A total of 1,124 ischemic stroke cases and 1,163 controls were genotyped with inflammatory panel strips containing 51 selected inflammatory gene polymorphisms from 35 candidate genes. We tested the genotype-stroke association with logistic regression model.

RESULTS

We found two single nucleotide polymorphisms (SNPs) in CCL11 were associated with ischemic stroke. After adjusting for multiple testing using false discovery rate (FDR) with a 0.20 cut-off point, CCL11 rs4795895 remained statistically significant. We further stratified the study population by their hypertension status. In the hypertensive group, CCR2 rs1799864, CCR5 rs1799987 and CCL11 rs4795895 were nominally associated with increased risk of stroke. In the non-hypertensive group, CCL11 rs3744508, LTC4S rs730012, FCER1B rs569108, TGFB1 rs1800469, LTA rs909253 and CCL11 rs4795895 were associated with ischemic stroke. After correction for multiple testing, CCR2 rs1799864 and CCR5 rs1799987 remained significant in the hypertensive group, and CCL11 rs3744508, LTC4S rs730012, FCER1B rs569108, TGFB1 rs1800469, LTA rs909253 remained significant in the non-hypertensive group.

CONCLUSIONS

Our results indicate that inflammatory genetic variants are associated with increased risk of ischemic stroke in a Chinese Han population, particularly in non-hypertensive individuals.

摘要

背景

炎症机制在中风风险中起重要作用,炎症反应成分中的遗传变异已被认为是中风的危险因素。我们在中国汉族人群中检测了炎症基因多态性及其与缺血性中风的关系。

方法

采用包含 35 个候选基因中 51 个炎症基因多态性的炎症基因谱试剂盒,对 1124 例缺血性中风病例和 1163 例对照进行基因分型。我们使用逻辑回归模型检测基因型与中风的相关性。

结果

我们发现 CCL11 中的两个单核苷酸多态性(SNP)与缺血性中风有关。在使用 FDR 进行多重检验校正(0.20 截断值)后,CCL11 rs4795895 仍然具有统计学意义。我们进一步根据高血压状态对研究人群进行分层。在高血压组中,CCR2 rs1799864、CCR5 rs1799987 和 CCL11 rs4795895 与中风风险增加呈名义相关。在非高血压组中,CCL11 rs3744508、LTC4S rs730012、FCER1B rs569108、TGFB1 rs1800469、LTA rs909253 和 CCL11 rs4795895 与缺血性中风相关。经过多重检验校正后,高血压组中 CCR2 rs1799864 和 CCR5 rs1799987 仍然显著,非高血压组中 CCL11 rs3744508、LTC4S rs730012、FCER1B rs569108、TGFB1 rs1800469、LTA rs909253 仍然显著。

结论

我们的研究结果表明,炎症遗传变异与中国汉族人群缺血性中风风险增加相关,尤其是在非高血压个体中。

相似文献

引用本文的文献

本文引用的文献

2
Genetic associations in diabetic nephropathy: a meta-analysis.糖尿病肾病的遗传关联:荟萃分析。
Diabetologia. 2011 Mar;54(3):544-53. doi: 10.1007/s00125-010-1996-1. Epub 2010 Dec 3.
10
Inflammation and ischaemic stroke.炎症与缺血性中风。
Curr Opin Neurol. 2007 Jun;20(3):334-42. doi: 10.1097/WCO.0b013e32813ba151.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验