Zito Francesco, Lowe Gordon D O, Rumley Ann, McMahon Alex D, Humphries Steve E
Centre for Cardiovascular Genetics, Royal Free and University College London Medical School, London WC1E 6JJ, UK.
Atherosclerosis. 2002 Nov;165(1):153-8. doi: 10.1016/s0021-9150(02)00196-x.
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.
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.
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).
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.
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。
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。
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)。
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。