Kelleher C C, Mitropoulos K A, Imeson J, Meade T W, Martin J C, Reeves B E, Hughes L O
MRC Epidemiology and Medical Care Unit, Wolfson Institute of Preventive Medicine, Medical College of St. Bartholomew's Hospital, London, UK.
Atherosclerosis. 1992 Nov;97(1):67-73. doi: 10.1016/0021-9150(92)90052-i.
In order to evaluate whether Hageman factor (XII) is increased in survivors of myocardial infarction and whether this in turn influences factor VII coagulant activity (VIIc), we examined the coagulation and lipoprotein profiles in 82 subjects, 51 of whom had a definite history of myocardial infarction and 31 healthy volunteers invited from a local general practice register for a cardiovascular screen. Both serum cholesterol (P = 0.03) and plasma fibrinogen levels (P = 0.02) were significantly elevated in cases compared with controls. There were no significant differences in coagulant activities, and in particular factor XII concentration was not significantly different between groups. Furthermore, in 47 of the subjects, 28 of whom had a history of myocardial infarction, a more detailed analysis, including measurement of VIIc after overnight incubation of plasma at 4 degrees C, was undertaken. Approximately half the subjects in either group showed some evidence of activation, though history of myocardial infarction was not in itself a significant predictor of this. All measures of XII concentration related positively to VIIc after cold activation, the strongest being the measure of amidolytic activity following activation of factor XII (XIIAm) (r = 0.5, P < 0.01). In addition, XIIa, a measure of activity due to enzymes derived from factor XII, related strongly to many of the measured lipoprotein variables, particularly VLDL cholesterol and triglycerides, supporting the hypothesis that negatively charged molecules such as free fatty acids on larger lipoprotein particles provide the contact surface necessary to activate factor XII. The findings confirm the importance of this alternative pathway in leading to activation of factor VII.
为了评估心肌梗死幸存者中凝血因子Ⅻ是否升高,以及这是否反过来影响凝血因子Ⅶ的凝血活性(Ⅶc),我们检测了82名受试者的凝血和脂蛋白谱,其中51名有明确的心肌梗死病史,31名是从当地普通诊所登记册中邀请来进行心血管筛查的健康志愿者。与对照组相比,病例组的血清胆固醇(P = 0.03)和血浆纤维蛋白原水平(P = 0.02)均显著升高。凝血活性方面无显著差异,特别是两组之间的凝血因子Ⅻ浓度无显著差异。此外,在47名受试者中,其中28名有心肌梗死病史,进行了更详细的分析,包括在4℃下将血浆过夜孵育后测量Ⅶc。两组中约一半的受试者显示出一些激活迹象,尽管心肌梗死病史本身并不是这种情况的显著预测因素。冷激活后,所有凝血因子Ⅻ浓度的测量指标均与Ⅶc呈正相关,最强的是凝血因子Ⅻ激活后的酰胺水解活性测量指标(ⅫAm)(r = 0.5,P < 0.01)。此外,凝血因子Ⅻa是凝血因子Ⅻ衍生酶活性的测量指标,与许多测量的脂蛋白变量密切相关,特别是极低密度脂蛋白胆固醇和甘油三酯,支持了这样一种假设,即较大脂蛋白颗粒上的游离脂肪酸等带负电荷分子提供了激活凝血因子Ⅻ所需的接触表面。这些发现证实了这条替代途径在导致凝血因子Ⅶ激活中的重要性。