Suppr超能文献

白细胞介素6基因-572C/G多态性与心肌梗死易感性的关联性研究

[Study on linkage between polymorphism of interleukin 6 gene -572C/G and susceptibility to myocardial infarction].

作者信息

Fu Hai-xia, Zhang Jia-ying, Li Geng-shan, Li Yan, Xu Jia-li, Zhao Zi-niu

机构信息

Department of Cardiology, Henan Provincial People's Hospital, Zhengzhou, Henan, 450003 PR China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Jun;23(3):245-9.

Abstract

OBJECTIVE

To observe the polymorphism and gene frequency of interleukin 6 (IL6) gene -572C/G in Chinese Han nationality population, that associating with susceptibility to myocardial infarction(MI) and impacting on the extent of coronary artery lesions; to analyze the function of IL6 gene -572C/G polymorphism.

METHODS

With PCR-RFLP method, IL6 gene -572C/G polymorphism was genotyped to 232 MI patients and 260 healthy adults. The effect of IL6 gene -572C/G polymorphism was observed to the extent of coronary artery lesions and the ability of IL6 production from peripheral blood mononuclear cells (PBMC).

RESULTS

There was IL6 gene -572C/G polymorphism in Chinese Hans. -572CG+GG genotype and G allele were more frequent in patients than in controls (P< 0.01). The relative risk for G allele carrier to suffer from MI was 1.68 times of CC genotype individual (95%CI 1.17-2.41, P< 0.01). However, the distribution of IL6 gene -572C/G polymorphism was no significant difference among patients with single-vessel, two-vessel and three-vessel lesions (P> 0.05). After PBMC cultured for 24 hours, the IL6 concentration in supernatant was significantly higher in subjects with CG genotype than those with CC genotype (P< 0.05).

CONCLUSION

IL6 gene -572G allele may be a genetic susceptibility factor to MI attack of Chinese Hans population, and related to the high expression of IL6.

摘要

目的

观察白细胞介素6(IL6)基因-572C/G在中国汉族人群中的多态性及基因频率,探讨其与心肌梗死(MI)易感性的关系以及对冠状动脉病变程度的影响;分析IL6基因-572C/G多态性的功能。

方法

采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,对232例MI患者和260例健康成年人进行IL6基因-572C/G多态性基因分型。观察IL6基因-572C/G多态性对冠状动脉病变程度及外周血单个核细胞(PBMC)产生IL6能力的影响。

结果

中国汉族人群存在IL6基因-572C/G多态性。患者中-572CG+GG基因型和G等位基因频率高于对照组(P<0.01)。G等位基因携带者患MI的相对风险是CC基因型个体的1.68倍(95%CI 1.17-2.41,P<0.01)。然而,IL6基因-572C/G多态性在单支、双支和三支血管病变患者中的分布无显著差异(P>0.05)。PBMC培养24小时后,CG基因型受试者上清液中IL6浓度显著高于CC基因型受试者(P<0.05)。

结论

IL6基因-572G等位基因可能是中国汉族人群MI发病的遗传易感因素,并与IL6的高表达有关。

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