Castellanos Mar, Leira Rogelio, Serena Joaquín, Blanco Miguel, Pedraza Salvador, Castillo José, Dávalos Antoni
Department of Neurology, Hospital Universitari Doctor Josep Trueta in affiliation with the UAB, Avda Francia s/n, Girona-17007, Spain.
Stroke. 2004 Jul;35(7):1671-6. doi: 10.1161/01.STR.0000131656.47979.39. Epub 2004 May 27.
Elevated plasma levels of cellular fibronectin (c-Fn) reflect vascular damage, so c-Fn might be a marker of secondary bleeding risk in cerebral ischemia. We investigated whether high plasma levels of c-Fn were associated with hemorrhagic transformation (HT) after treatment with tissue plasminogen activator (tPA) in patients with acute stroke.
Eighty-seven patients (mean age: 67+/-12) received tPA after the ECASS II criteria (mean time to infusion: 160+/-46 minutes; median NIHSS: 12). HT and hypodensity volume were studied on computed tomography (CT) performed 24 to 36 hours after treatment. HT was classified according to the ECASS II definitions. c-Fn and matrix metalloproteinase 9 (MMP-9) levels were determined by ELISA in blood samples obtained before treatment and in 30 healthy subjects.
HT was found in 26 patients (30%); 15 patients had hemorrhagic infarction type 1 (HI-1), 7 had HI-2, and 4 had parenchymal hemorrhage (PH). Median c-Fn concentrations were 1.3, 1.7, 4.2, 5.4, and 7.3 microg/mL in controls, non-HT, HI-1, HI-2, and PH groups, respectively (P<0.001); median MMP-9 values were 54, 87, 154, 176, and 225 ng/mL (P<0.001). Logistic regression analysis showed that only c-Fn plasma levels remained independently associated with HT after adjusting for potential confounders (OR, 2.1; 95% CI, 1.3 to 3.4; P=0.002). Similar results were obtained in the 71 patients treated within 3 hours.
High plasma c-Fn levels are significantly associated with subsequent HT in stroke patients treated with tPA, so plasma c-Fn determinations might be useful in clinical practice to improve the risk/benefit ratio of thrombolytic treatment.
血浆中细胞纤连蛋白(c-Fn)水平升高反映血管损伤,因此c-Fn可能是脑缺血继发性出血风险的一个标志物。我们研究了急性卒中患者接受组织型纤溶酶原激活剂(tPA)治疗后,血浆中高浓度的c-Fn是否与出血性转化(HT)相关。
87例患者(平均年龄:67±12岁)符合欧洲急性卒中协作研究II(ECASS II)标准后接受tPA治疗(平均输注时间:160±46分钟;美国国立卫生研究院卒中量表[NIHSS]中位数:12)。在治疗后24至36小时进行计算机断层扫描(CT),研究HT和低密度体积。HT根据ECASS II的定义进行分类。通过酶联免疫吸附测定(ELISA)法测定治疗前采集的血样以及30名健康受试者血样中的c-Fn和基质金属蛋白酶9(MMP-9)水平。
26例患者(30%)出现HT;15例为1型出血性梗死(HI-1),7例为HI-2,4例为实质出血(PH)。对照组、非HT组、HI-1组、HI-2组和PH组的c-Fn浓度中位数分别为1.3、1.7、4.2、5.4和7.3μg/mL(P<0.001);MMP-9值中位数分别为54、87、154、176和225 ng/mL(P<0.001)。多因素逻辑回归分析显示,在对潜在混杂因素进行校正后,仅血浆c-Fn水平仍与HT独立相关(比值比[OR],2.1;95%置信区间[CI],1.3至3.4;P=0.002)。在3小时内接受治疗的71例患者中也得到了类似结果。
在接受tPA治疗的卒中患者中,血浆c-Fn水平升高与随后的HT显著相关,因此测定血浆c-Fn可能有助于临床实践中改善溶栓治疗的风险/效益比。