Schillinger Martin, Exner Markus, Sabeti Schila, Mlekusch Wolfgang, Amighi Jasmin, Handler Sylvia, Quehenberger Peter, Kalifeh Neda, Wagner Oswald, Minar Erich
Department of Angiology, Medical University Vienna, Waehringer Guertel 18-20, A-1090 Vienna, Austria.
Thromb Haemost. 2004 Nov;92(5):1108-13. doi: 10.1160/TH04-05-0311.
High heparin cofactor II (HCII) activity has recently been described to protect from coronary instent restenosis, presumably by inactivating thrombin in injured arteries. In this study, we investigated the association of HCII activity and restenosis after femoropopliteal stenting. We studied 63 consecutive patients with peripheral artery disease who underwent femoropopliteal stent implantation after initial failure of plain balloon angioplasty due to a significant residual stenosis (>30% lumen diameter reduction) or a flow limiting dissection. HCII activity was measured before stenting and patients were followed for median 10 months (interquartile range 6 to 17) for the occurrence of a first instent restenosis, defined as a >50% lumen diameter reduction by color coded duplex sonography and confirmed by angiography. Cumulative freedom from restenosis at 6 and 12 months in patients with lower HCII activity (100%, lower tertile, n=20) was 84% and 35% as compared to 93% and 72% in patients with high HCII activity (>100%, middle and upper tertile, n=43; p=0.024 by Log Rank test). Adjusting for the material of the implanted stents (nitinol vs. Wallstents), patients with a high HCII activity had a 0.39-fold reduced risk for instent restenosis (95% CI 0.17 to 0.90, p=0.028), additional adjustment for diabetes mellitus, poor run-off, critical limb ischemia and cumulative length of the stented segment did not alter the observed effect. Higher activity of heparin cofactor II may exert a protective effect against instent restenosis also in the femoropopliteal vessel area, confirming a prior observation after coronary stenting.
最近有研究表明,高肝素辅因子II(HCII)活性可预防冠状动脉支架再狭窄,可能是通过使受损动脉中的凝血酶失活来实现的。在本研究中,我们调查了股腘动脉支架置入术后HCII活性与再狭窄之间的关系。我们研究了63例连续性外周动脉疾病患者,这些患者因严重残余狭窄(管腔直径减少>30%)或限流性夹层导致单纯球囊血管成形术初始失败后接受了股腘动脉支架植入术。在支架置入术前测量HCII活性,并对患者进行中位数为10个月(四分位间距为6至17个月)的随访,观察首次支架内再狭窄的发生情况,首次支架内再狭窄定义为彩色编码双功超声显示管腔直径减少>50%,并经血管造影证实。HCII活性较低(100%,较低三分位数,n = 20)的患者在6个月和12个月时的累积无再狭窄率分别为84%和35%,而HCII活性较高(>100%,中间和较高三分位数,n = 43)的患者为93%和72%(对数秩检验p = 0.024)。在调整植入支架的材料(镍钛合金支架与Wallstents支架)后,HCII活性高的患者发生支架内再狭窄的风险降低了0.39倍(95%CI 0.17至0.90,p = 0.028),进一步调整糖尿病、流出道不良、严重肢体缺血和支架置入段的累积长度后,观察到的效果未改变。肝素辅因子II的较高活性可能对股腘血管区域的支架内再狭窄也具有保护作用,这证实了冠状动脉支架置入术后的先前观察结果。