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在WOSCOPS研究中,凝血因子XII 46C>T基因多态性与冠心病(CHD)风险的关联。

Association of the factor XII 46C>T polymorphism with risk of coronary heart disease (CHD) in the WOSCOPS study.

作者信息

Zito Francesco, Lowe Gordon D O, Rumley Ann, McMahon Alex D, Humphries Steve E

机构信息

Centre for Cardiovascular Genetics, Royal Free and University College London Medical School, London WC1E 6JJ, UK.

出版信息

Atherosclerosis. 2002 Nov;165(1):153-8. doi: 10.1016/s0021-9150(02)00196-x.

Abstract

AIM

To evaluate the contribution of the 46C>T polymorphism of the Factor XII (FXII) gene to risk for coronary heart disease (CHD) in the West of Scotland Coronary Prevention Study (WOSCOPS) of men with high cholesterol.

BACKGROUND

WOSCOPS is a primary prevention trial that demonstrated the effectiveness of pravastatin in reducing morbidity and mortality from CHD. FXII is a protein of the contact system that plays a key role in both coagulation and fibrinolysis. Elevated activated FXII (FXIIa) levels have been previously associated with CHD. Plasma FXIIa levels are strongly determined by a 46C>T polymorphism in the FXII gene.

RESULTS

441 CHD cases and 990 controls were genotyped. The frequency of TT homozygotes was 8.3% in controls and 11.8% in cases (P=0.04). When compared with the CC+CT group (after adjustment for age, blood pressure, BMI, fibrinogen and lipid levels) the TT genotype was an independent risk factor for CHD (OR 1.48 95% CI 1.01-2.17), an effect that was only significant in the pravastatin group (OR 1.95 95% CI 1.09-3.47) and not in the placebo group (OR 1.20, 95%CI 0.72-2.02). Compared with risk in the placebo group as a whole (reference group), and after adjustment for other risk factors, men with the CC or CT genotype, but not the TT genotype showed a significant benefit from pravastatin treatment (OR, respectively, 0.61 (0.46-0.81) and 0.56 (0.40-0.79) compared with 1.10 (0.64-1.96). In a subgroup of these men, subjects with the TT genotype had, as expected, baseline levels of FXIIa that were 50% lower than those with the CC genotype, with CT subjects having intermediate levels (P<0.001 by Kruskal-Wallis test).

CONCLUSIONS

The TT genotype of the FXII 46C>T polymorphism is associated with a high risk of CHD in men with high cholesterol. We hypothesise that reduced fibrinolysis in these men, as a consequence of lower plasma FXIIa, may be the mechanism leading to higher risk, and that pravastatin treatment may enhance this effect.

摘要

目的

在苏格兰西部冠心病预防研究(WOSCOPS)中,评估高胆固醇男性人群中凝血因子 XII(FXII)基因46C>T多态性对冠心病(CHD)风险的影响。

背景

WOSCOPS是一项一级预防试验,证实了普伐他汀在降低冠心病发病率和死亡率方面的有效性。FXII是接触系统中的一种蛋白质,在凝血和纤维蛋白溶解过程中起关键作用。此前,活化的FXII(FXIIa)水平升高与冠心病有关。血浆FXIIa水平很大程度上由FXII基因中的46C>T多态性决定。

结果

对441例冠心病患者和990例对照进行基因分型。TT纯合子在对照组中的频率为8.3%,在病例组中为11.8%(P = 0.04)。与CC + CT组相比(调整年龄、血压、体重指数、纤维蛋白原和血脂水平后),TT基因型是冠心病的独立危险因素(OR 1.48,95%CI 1.01 - 2.17),这种效应仅在普伐他汀组中显著(OR 1.95,95%CI 1.09 - 3.47),而在安慰剂组中不显著(OR 1.20,95%CI 0.72 - 2.02)。与整个安慰剂组(参照组)的风险相比,并调整其他危险因素后,CC或CT基因型的男性,但不是TT基因型的男性,从普伐他汀治疗中显示出显著益处(OR分别为0.61(0.46 - 0.81)和0.56(0.40 - 0.79),而TT基因型男性为1.10(0.64 - 1.96))。在这些男性的一个亚组中,正如预期的那样,TT基因型受试者的FXIIa基线水平比CC基因型受试者低50%,CT基因型受试者的水平处于中间(经Kruskal - Wallis检验,P < 0.001)。

结论

FXII基因46C>T多态性的TT基因型与高胆固醇男性患冠心病的高风险相关。我们推测,这些男性由于血浆FXIIa水平较低导致纤维蛋白溶解减少,可能是导致风险升高的机制,并且普伐他汀治疗可能会增强这种效应。

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