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[C反应蛋白基因C1444T多态性与健康人和心肌梗死患者血清C反应蛋白浓度]

[Polymorphism C1444T of C-reactive protein gene and C-reactive protein concentration in blood serum of healthy people and patients with myocardial infarction].

作者信息

Shakhnovich P M, Sukhinina T S, Barsova R M, Sudomoina M A, Rybalkin I N, Shreĭder E V, Vlasik T N, Favorova O O, Ruda M Ia

出版信息

Kardiologiia. 2010;50(8):4-12.

Abstract

UNLABELLED

CRP level is a risk factor of development of ischemic heart disease (IHD) and acute myocardial infarction (MI) in healthy people, while in patients with cardiovascular diseases it is a marker of unfavorable prognosis. It has been shown in recent investigations that individual variations of plasma CRP levels to a great extent are genetically determined. These data constitute a basis for the study of associations of polymorphic variants of the CRP gene with risk of MI in healthy people as well as with unfavorable prognosis in IHD patients.

MATERIAL AND METHODS

We included into the study 232 Russian patients aged 52.3 +/- 10.3 years, 175 men (50.1 +/- 10.6 years) and 57 women (55.2 +/- 10.1 years). Control group comprised 159 Russians without history of cardiovascular diseases and other serious severe concomitant diseases (age 60.5 +/- 14 years), 76 men (age 57.3 +/- 13.9 years ) and 83 women (age 63.1 +/- 14 years). CRP concentration was measured initially (at the moment of hospitalization), on days 3, at discharge, in 1 and 6 months, 1 year after onset of infarction. For genomic typing of C1444T polymorphism of CRP gene we used restriction fragment length analysis of products of polymerase chain reaction (PCR).

RESULTS

Distribution of genotypes of C1444T polymorphism of CRP gene: C/C 51.8%, C/T 35.8%, T/T 12.4% in patients with MI; C/C 55.2%, C/T 40.2%, T/T 4.6% in control group. We found significant difference (p = 0.006, relative risk [RR] 0.3, 95% confidence interval [CI] 0.15-0.74) in frequency of carriers of C1444 allele (sum of C/C and C/T genotypes), which was higher in control group. Correspondingly in the group of patients with MI T/T genotype was met significantly more frequently than in control (p = 0.006, RR 3.0, 95% CI 1.3-6.5), and can be looked upon as risk factor of MI. We found no relation between carriage of CRP alleles/genotypes of CRP and one year prognosis in patients with MI. Analysis of association of the C1444T polymorphism with CRP concentration revealed significant relationship between T/T genotype and higher CRP level.

摘要

未标记

在健康人群中,CRP水平是缺血性心脏病(IHD)和急性心肌梗死(MI)发生的危险因素,而在心血管疾病患者中,它是预后不良的标志物。最近的研究表明,血浆CRP水平的个体差异在很大程度上是由基因决定的。这些数据为研究CRP基因多态性变体与健康人群MI风险以及IHD患者不良预后之间的关联奠定了基础。

材料与方法

我们纳入了232名俄罗斯患者,年龄为52.3±10.3岁,其中男性175名(50.1±10.6岁),女性57名(55.2±10.1岁)。对照组包括159名无心血管疾病史和其他严重伴随疾病的俄罗斯人(年龄60.5±14岁),其中男性76名(年龄57.3±13.9岁),女性83名(年龄63.1±14岁)。在梗死发作后的最初(住院时)、第3天、出院时、1个月和6个月、1年测量CRP浓度。对于CRP基因C1444T多态性的基因分型,我们使用聚合酶链反应(PCR)产物的限制性片段长度分析。

结果

MI患者中CRP基因C1444T多态性的基因型分布:C/C为51.8%,C/T为35.8%,T/T为12.4%;对照组中C/C为55.2%,C/T为40.2%,T/T为4.6%。我们发现C1444等位基因携带者(C/C和C/T基因型之和)的频率存在显著差异(p = 0.006,相对风险[RR] 0.3,95%置信区间[CI] 0.15 - 0.74),对照组中的频率更高。相应地,MI患者组中T/T基因型的出现频率显著高于对照组(p = 0.006,RR 3.0,95% CI 1.3 - 6.5),可被视为MI的危险因素。我们未发现CRP等位基因/基因型携带与MI患者1年预后之间的关系。C1444T多态性与CRP浓度的关联分析显示T/T基因型与较高的CRP水平之间存在显著关系。

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