摘要
目的探讨冠状动脉粥样硬化性心脏病(简称冠心病)患者血白细胞分化抗原14(CD14)基因C(-260)T多态性与血清超敏C反应蛋白(Hs-CRP)水平的关系。方法对240例冠心病患者应用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术检测CD14基因多态性并测定Hs-CRP水平,分析两者之间的关系。结果240例冠心病患者CD14基因C(-260)T多态性:呈TT基因型106例(44.2%)、TC基因型82例(34.1%)、CC基因型52例(21.7%)。Hs-CRP水平:TT基因型患者Hs-CRP(4.5±2.1)mg/L与TC基因型患者[(2.7±1.2)mg/L]及CC基因型患者[(2.9±1.1)mg/L]比较差异有统计学意义(t=10.10、8.85,均P<0.05):Hs-CRP>3.0mg/L的TT基因型高危患者占79.2%,与TC基因型高危患者(50.00%)及CC基因型高危患者(36.5%)比较,差异有统计学意义(χ2=17.75、28.04,均P<0.05)。结论T等位基因纯合子可能是冠心病炎症反应的独立影响因素,CD14基因变异可能与冠心病炎症反应有关。
Objective To investigate the relationship of serum levels of high sensitivity C-reactive protein (Hs-CRP) with CD14 C-260T promoter polymorphism in patients with coronary heart disease (CHD). Methods Serum levels of Hs-CRP were determined in 240 patients with coronary heart disease. C-260T promoter polymorphism of the CD14 gene was screened by PCR-RELP assay. Results The genotype distribution of the C-260T polymorphism of the CD14 gene was as follows:TT in 106 of 240 patients (44. 2% ), TC in 82 of 240 patients(34. 1% ) and CC in 52 of 240 patients(21.7% ). Patients with TI' subtype had increased Hs-CRP levels compared with carriers of the C allele ( P〈0. 05 ) . A higher percentage of T allele homozygotes had Hs-CRP levels 〉3 mg/L (P〈0. 05 ). Conclusion This study indicated T allele homozygotes of CD14 gene may be an inde- pendent risk factor in systemic inflammation with stable CHD.
出处
《四川医学》
CAS
2009年第8期1313-1315,共3页
Sichuan Medical Journal