UCLA Stroke Center, Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.
J Neurol Sci. 2012 Feb 15;313(1-2):142-6. doi: 10.1016/j.jns.2011.08.048. Epub 2011 Sep 25.
Early disruption of the blood-brain barrier (BBB) due to severe ischemia can be detected by MRI T2* permeability imaging. In middle cerebral artery (MCA) infarction, pretreatment T2* permeability derangements have been found in 22% of patients and are powerful predictors of hemorrhagic transformation after revascularization therapy. The frequency, clinical correlates, and relation to hemorrhagic transformation of permeability derangements in posterior circulation have not been previously explored, and may differ as ischemia volume and collateral status are different between vertebrobasilar and MCA infarcts.
We analyzed clinical and pretreatment MRI data on consecutive patients undergoing recanalization therapy for acute vertebrobasilar ischemia at a medical center November 2001 through September 2009. Pretreatment MRI permeability images were derived from perfusion source imaging acquisitions. Permeability abnormality was detected as persisting increased signal intensity at later time points in perfusion MRI acquisition, indicating local accumulation of contrast caused by BBB leakage.
Among the 14 patients meeting study entry criteria, mean age was 71.1 years and median pretreatment NIHSS was 20.5. Permeability imaging abnormality was present in 1 of the 14 patients (7%). Among 14 patients, post-treatment parenchymal hematoma occurred in one and more minor degrees of hemorrhagic transformation in four. The one patient with pretreatment permeability abnormality was the patient to develop post-treatment parenchymal hematoma (Fisher's exact test, P=0.07).
Pretreatment permeability abnormality, an indicator of BBB derangements, is an infrequent finding in acute posterior circulation ischemic stroke and may be associated with an increased risk of parenchymal hematoma development undergoing recanalization therapy.
由于严重的缺血,血脑屏障(BBB)的早期破坏可以通过 MRI T2通透性成像检测到。在大脑中动脉(MCA)梗死中,已经在 22%的患者中发现了预处理 T2通透性紊乱,并且是血管再通治疗后出血转化的有力预测指标。尚未探索过后循环通透性紊乱的频率、临床相关性及其与出血转化的关系,并且由于椎基底动脉和 MCA 梗死之间的缺血体积和侧支状态不同,可能会有所不同。
我们分析了 2001 年 11 月至 2009 年 9 月在医疗中心接受急性椎基底动脉缺血再通治疗的连续患者的临床和预处理 MRI 数据。预处理 MRI 通透性图像是从灌注源成像采集衍生而来的。通透性异常是通过在灌注 MRI 采集的后期时间点检测到持续增加的信号强度来检测到的,这表明由于 BBB 渗漏导致局部对比剂积聚。
在符合研究纳入标准的 14 例患者中,平均年龄为 71.1 岁,预处理 NIHSS 中位数为 20.5。14 例患者中有 1 例(7%)存在通透性成像异常。在 14 例患者中,有 1 例发生治疗后实质血肿,4 例发生更轻微程度的出血转化。在接受预处理通透性异常的 1 例患者中,发生了治疗后实质血肿(Fisher 确切检验,P=0.07)。
BBB 紊乱的指标——预处理通透性异常在急性后循环缺血性脑卒中中是一种罕见的发现,并且可能与接受再通治疗后实质血肿发展的风险增加有关。