McGarry Bryony L, Jokivarsi Kimmo T, Knight Michael J, Grohn Olli H J, Kauppinen Risto A
School of Experimental Psychology and Clinical Research and Imaging Center Bristol, University of Bristol, Bristol, UK.
Department of Neurobiology, A.I. Virtanen Institute, University of Eastern Finland, Kuopio, Finland.
J Vis Exp. 2017 Sep;2017(127). doi: 10.3791/55277. Epub 2017 Sep 16.
MRI provides a sensitive and specific imaging tool to detect acute ischemic stroke by means of a reduced diffusion coefficient of brain water. In a rat model of ischemic stroke, differences in quantitative T and T MRI relaxation times (qT and qT) between the ischemic lesion (delineated by low diffusion) and the contralateral non-ischemic hemisphere increase with time from stroke onset. The time dependency of MRI relaxation time differences is heuristically described by a linear function and thus provides a simple estimate of stroke onset time. Additionally, the volumes of abnormal qT and qT within the ischemic lesion increase linearly with time providing a complementary method for stroke timing. A (semi)automated computer routine based on the quantified diffusion coefficient is presented to delineate acute ischemic stroke tissue in rat ischemia. This routine also determines hemispheric differences in qT and qT relaxation times and the location and volume of abnormal qT and qT voxels within the lesion. Uncertainties associated with onset time estimates of qT and qT MRI data vary from ± 25 min to ± 47 min for the first 5 hours of stroke. The most accurate onset time estimates can be obtained by quantifying the volume of overlapping abnormal qT and qT lesion volumes, termed 'V' (± 25 min) or by quantifying hemispheric differences in qT relaxation times only (± 28 min). Overall, qT derived parameters outperform those from qT. The current MRI protocol is tested in the hyperacute phase of a permanent focal ischemia model, which may not be applicable to transient focal brain ischemia.
磁共振成像(MRI)通过检测脑水扩散系数降低,提供了一种灵敏且特异的成像工具来检测急性缺血性中风。在缺血性中风大鼠模型中,缺血性病变(由低扩散率描绘)与对侧非缺血性半球之间的定量T1和T2 MRI弛豫时间(qT1和qT2)差异随中风发作后的时间而增加。MRI弛豫时间差异的时间依赖性可通过线性函数进行经验性描述,从而提供中风发作时间的简单估计。此外,缺血性病变内异常qT1和qT2的体积随时间呈线性增加,为中风时间判断提供了一种补充方法。本文提出了一种基于量化扩散系数的(半)自动化计算机程序,用于在大鼠缺血模型中描绘急性缺血性中风组织。该程序还可确定qT1和qT2弛豫时间的半球差异以及病变内异常qT1和qT2体素的位置和体积。对于中风后的前5小时,与qT1和qT2 MRI数据发作时间估计相关的不确定性在±25分钟至±47分钟之间变化。通过量化重叠的异常qT1和qT2病变体积(称为“V”,±25分钟)或仅通过量化qT1弛豫时间的半球差异(±28分钟),可获得最准确的发作时间估计。总体而言,qT1衍生参数优于qT2衍生参数。当前的MRI方案在永久性局灶性缺血模型的超急性期进行了测试,该模型可能不适用于短暂性局灶性脑缺血。