Department of Clinical Biochemistry, State Key Laboratory of Kidney Disease, Chinese PLA General Hospital, 100853 Beijing, China.
BMC Cardiovasc Disord. 2012 Jul 10;12:51. doi: 10.1186/1471-2261-12-51.
Studies have demonstrated that inflammation has a key role in the pathogenesis of atherosclerosis due to the abnormal gene expressions of multiple cytokines. We established an accurate and precise method to observe gene expression in whole blood that might provide specific diagnostic information for coronary artery disease (CAD) and other related diseases.
The fifteen selected CAD-related genes (IL1B, IL6, IL8, IFNG, MCP-1, VWF, MTHFR, SELL, TNFalpha, ubiquitin, MCSF, ICAM1, ID2, HMOX1 and LDLR) and two housekeeping genes (ACTB and GK) as internal references have been measured simultaneously with a newly developed multiplex polymerase chain reaction (multi-PCR) method. Moreover, the precision was evaluated, and a procedure for distinguishing patients from the normal population has been developed based upon analyses of peripheral blood. A total of 148 subjects were divided into group A (control group without plaques), group B (calcified plaques) and group C (non-calcified plaques, and combination group) according dual-source CT criteria. Gene expression in blood was analyzed by multi-PCR, and levels of glucose and lipids measured in 50 subjects to explore the relationship among them.
The precision results of the multi-PCR system revealed within-run and between-run CV values of 3.695-12.537% and 4.405-13.405%, respectively. The profiles of cytokine gene expression in peripheral blood were set: a positive correlation between glucose and MCSF, HMOX1 or TNFalpha were found. We also found that triglyceride levels were negatively correlated with SELL gene expression in 50 subjects. Compared with controls, gene expression levels of IL1B, IL6, IL8 and MCP-1 increased significantly in group C.
A new multiple gene expression analysis system has been developed. The primary data suggested that gene expression was related to CAD. This system might be used for risk assessment of CVDs and other related diseases.
研究表明,由于多种细胞因子的异常基因表达,炎症在动脉粥样硬化的发病机制中起着关键作用。我们建立了一种准确而精确的方法来观察全血中的基因表达,这可能为冠心病(CAD)和其他相关疾病提供特定的诊断信息。
同时使用新开发的多重聚合酶链反应(multi-PCR)方法测量了 15 个与 CAD 相关的基因(IL1B、IL6、IL8、IFNG、MCP-1、VWF、MTHFR、SELL、TNFalpha、泛素、MCSF、ICAM1、ID2、HMOX1 和 LDLR)和两个管家基因(ACTB 和 GK)。此外,评估了精度,并根据外周血分析开发了一种区分患者和正常人群的程序。根据双源 CT 标准,将 148 例患者分为 A 组(无斑块对照组)、B 组(钙化斑块组)和 C 组(非钙化斑块组和混合组)。通过 multi-PCR 分析血液中的基因表达,并测量 50 例患者的血糖和血脂水平,以探讨它们之间的关系。
multi-PCR 系统的精度结果显示,其在运行内和运行间的 CV 值分别为 3.695-12.537%和 4.405-13.405%。外周血细胞因子基因表达谱设置为:发现葡萄糖与 MCSF、HMOX1 或 TNFalpha 之间存在正相关。我们还发现,在 50 例患者中,甘油三酯水平与 SELL 基因表达呈负相关。与对照组相比,C 组的 IL1B、IL6、IL8 和 MCP-1 基因表达水平显著升高。
我们开发了一种新的多基因表达分析系统。初步数据表明,基因表达与 CAD 有关。该系统可用于 CVD 及其他相关疾病的风险评估。