Meade T W, Ruddock V, Stirling Y, Chakrabarti R, Miller G J
MRC Epidemiology and Medical Care Unit, Wolfson Institute of Preventive Medicine, Medical College of St Bartholomew's Hospital, London, UK.
Lancet. 1993 Oct 30;342(8879):1076-9. doi: 10.1016/0140-6736(93)92062-x.
Fibrinolytic activity (FA) was measured by dilute blood clot lysis time at entry to the Northwick Park Heart Study in 1382 white men aged 40-64, of whom 179 subsequently experienced episodes of ischaemic heart disease during a mean follow-up period of 16.1 years. There was a significant interaction between age and low FA (p = 0.02) with respect to ischaemic heart disease: a difference of one standard deviation in FA was associated with a difference of about 40% in ischaemic heart disease risk (p = 0.002) in those aged 40-54 at entry. The FA association remained after adjusting for plasma fibrinogen. High fibrinogen concentrations themselves were also associated with ischaemic heart disease, as was high factor VII activity with fatal events. Low FA in younger men may exert a long-term influence by impairing the removal of fibrin deposits that contribute to atherogenesis. Low FA appears to be a leading determinant of ischaemic heart disease in younger men and methods of enhancing fibrinolytic activity, whether by life-style changes or pharmacologically, should be considered.
在诺思威克公园心脏研究开始时,对1382名年龄在40至64岁的白人男性测定了纤溶活性(FA),方法是采用稀释血块溶解时间。其中179人在平均16.1年的随访期内随后发生了缺血性心脏病发作。就缺血性心脏病而言,年龄与低FA之间存在显著交互作用(p = 0.02):在研究开始时年龄为40至54岁的人群中,FA相差一个标准差与缺血性心脏病风险相差约40%相关(p = 0.002)。在调整血浆纤维蛋白原后,FA的关联仍然存在。高纤维蛋白原浓度本身也与缺血性心脏病相关,高因子VII活性与致命事件相关。年轻男性的低FA可能通过损害有助于动脉粥样硬化形成的纤维蛋白沉积物的清除而产生长期影响。低FA似乎是年轻男性缺血性心脏病的主要决定因素,应考虑通过改变生活方式或药物手段来提高纤溶活性的方法。