Endler G, Marsik C, Jilma B, Schickbauer T, Quehenberger P, Mannhalter C
Clinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Vienna, Vienna, Austria.
J Thromb Haemost. 2007 Jun;5(6):1143-8. doi: 10.1111/j.1538-7836.2007.02530.x.
The clinical relevance of decreased coagulation factor XII (FXII) plasma activity as a risk factor for both venous and arterial thrombosis is still discussed controversially. The current study evaluated the predictive value of FXII levels for all-cause mortality in a large Viennese patient cohort.
Individuals, whose FXII activity levels were determined for suspected coagulation disorders or thrombophilia screening between 1991-2003 were included in this study (n = 8936, 51% male, 49% female, median age 43 years). Death/survival was determined by record linkage with the Austrian Death Registry. The median observation period was 5 years covering a total of 46 400 person years; the death rate was 17.1%. For Cox regression analysis, FXII plasma activity was divided into 11 categories of 10% steps with the category of > 100% FXII serving as a reference category.
With decreasing FXII plasma activity, hazard ratios for all-cause mortality gradually increased linearly from 1.0 in the > 100% category to 1.5 (95% CI: 1.2-1.9) in the 80-90% category to 4.7 (95% CI: 3.4-6.5) in the 10-20% category. Similar results were obtained, when only vascular mortality or death as a result of ischemic heart disease was considered. No significant increase in all-cause mortality (HR: 1.4, 95%CI 0.7-2.8) was observed in the small group of FXII-deficient subjects [0-10% category (n = 58)].
This study first demonstrates a strong and almost linear association of FXII plasma activity between 90% and 10% with all-cause mortality in a large Viennese patient cohort. Interestingly, mortality rates are not increased when FXII activity is below 10%, resulting in a U-shaped survival curve.
凝血因子XII(FXII)血浆活性降低作为静脉和动脉血栓形成的危险因素,其临床相关性仍存在争议。本研究评估了FXII水平对维也纳一个大型患者队列全因死亡率的预测价值。
本研究纳入了1991年至2003年间因疑似凝血障碍或血栓形成倾向筛查而测定FXII活性水平的个体(n = 8936,男性51%,女性49%,中位年龄43岁)。通过与奥地利死亡登记处的记录链接确定死亡/存活情况。中位观察期为5年,共计46400人年;死亡率为17.1%。对于Cox回归分析,FXII血浆活性被分为11个类别,以10%的步长划分,FXII > 100%的类别作为参考类别。
随着FXII血浆活性降低,全因死亡率的风险比从FXII > 100%类别中的1.0逐渐线性增加至80 - 90%类别中的1.5(95%置信区间:1.2 - 1.9),再到10 - 20%类别中的4.7(95%置信区间:3.4 - 6.5)。当仅考虑血管性死亡率或缺血性心脏病导致的死亡时,也得到了类似结果。在一小部分FXII缺乏的受试者[0 - 10%类别(n = 58)]中,未观察到全因死亡率有显著增加(风险比:1.4,95%置信区间0.7 - 2.8)。
本研究首次在维也纳一个大型患者队列中证明了FXII血浆活性在90%至10%之间与全因死亡率存在强烈且几乎呈线性的关联。有趣的是,当FXII活性低于10%时死亡率并未增加,从而形成了一条U形生存曲线。