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酰化刺激蛋白及其受体基因多态性与汉族和回族人群冠心病的关联

Association of acylation-stimulating protein and receptor gene polymorphisms with coronary heart disease in Han and Hui populations.

作者信息

Jiang Honglei, Liu Xiangju, Wang Dong, Guo Fang, Liu Jidong, Liang Xiaotang, Xing Zhaoqin, Cao Chunlin

机构信息

Department of Cardiology, Shandong Provincial Hospital Affiliated to Shandong University Jinan 250021, Shandong, China.

Department of Geriatrics, Qilu Hospital of Shandong University Jinan 250012, Shandong, China.

出版信息

Int J Clin Exp Med. 2015 Oct 15;8(10):18779-85. eCollection 2015.

Abstract

OBJECTIVE

This study was to analyze the acylation-stimulating protein (ASP) (301T>C) and C5a-like receptor 2 (C5L2) (698C>T) gene polymorphisms in Han and Hui populations, and investigate their association with coronary heart disease (CHD).

METHODS

245 Han CHD patients and 110 Hui CHD patients from Shandong, Jinan, China were included in this study. Biochemical analysis was performed to assess the blood sugar and lipid levels in these patients, and the TaqMan genotyping assay was used to determine the genotype distribution.

RESULTS

Our results showed that the C allele frequency in the ASP (301T>C) polymorphism in the Hui population was significantly higher than normal controls, while no significant differences were observed in the Han population, which might contribute to the genetic susceptibility of CHD in the Hui population. Moreover, for C5L2 (698C>T) gene polymorphism in both Han and Hui populations, the frequencies of the C/T genotype and T allele were significantly higher in the CHD patients compared with normal controls. Moreover, there were slight differences in the association of ASP and C5L2 gene polymorphisms with blood sugar and lipid levels between Han and Hui populations.

CONCLUSIONS

Our results suggest differential ASP and C5L2 genotype distributions between Han and Hui patients, which might be associated with the different CHD-related genetic susceptibilities in these populations. These findings might contribute to a better understanding of the etiology and pathogenesis of CHD in different regions and populations.

摘要

目的

本研究旨在分析汉族和回族人群中酰化刺激蛋白(ASP)(301T>C)和C5a样受体2(C5L2)(698C>T)基因多态性,并探讨它们与冠心病(CHD)的关联。

方法

本研究纳入了来自中国济南山东的245例汉族冠心病患者和110例回族冠心病患者。进行生化分析以评估这些患者的血糖和血脂水平,并使用TaqMan基因分型测定法确定基因型分布。

结果

我们的结果显示,回族人群中ASP(301T>C)多态性的C等位基因频率显著高于正常对照组,而汉族人群中未观察到显著差异,这可能导致回族人群中冠心病的遗传易感性。此外,对于汉族和回族人群中的C5L2(698C>T)基因多态性,与正常对照组相比,冠心病患者中C/T基因型和T等位基因的频率显著更高。此外,汉族和回族人群中ASP和C5L2基因多态性与血糖和血脂水平的关联存在细微差异。

结论

我们的结果表明汉族和回族患者之间ASP和C5L2基因型分布存在差异,这可能与这些人群中不同的冠心病相关遗传易感性有关。这些发现可能有助于更好地理解不同地区和人群中冠心病的病因和发病机制。

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