Wild J M, Wardlaw J M, Marshall I, Warlow C P
Department of Medical Physics, University of Edinburgh, Western General Hospital, Edinburgh, UK.
Stroke. 2000 Dec;31(12):3008-14. doi: 10.1161/01.str.31.12.3008.
It is generally considered that tissue that appears abnormal on T2 MRI is already infarcted and that any penumbra lies outside the T2-visible lesion. We investigated the distribution of infarcted tissue using proton spectroscopic MRI.
In patients with symptoms of acute hemispheric ischemic stroke, imaged within a maximum of 3 days of stroke, we explored the distribution of N:-acetylaspartate (NAA), a marker of intact neurons, within and around the abnormal (hyperintense) areas on T2-weighted MR images, using proton spectroscopic MRI.
In 11 patients, imaged 24 to 72 hours after stroke onset, there was little evidence of damaged neurons (reduced NAA) beyond the margins of hyperintensity on the T2 image. However, within the abnormal T2 area, there were statistically significant differences in the amount of NAA (ie, the proportion of intact neurons) between areas that were obviously abnormal on T2 (very hyperintense) and those that were only slightly abnormal (slightly hyperintense).
The extent and degree of hyperintensity of the T2-visible lesion directly reflect the amount of neuronal damage; lack of a T2-visible lesion would suggest predominantly intact neurons at the time of imaging. We hypothesize that once tissue damage has reached a critical (probably irreversible) level, the T2 image quickly becomes abnormal without any significant time lag between the pathological staging of the infarct and its visualization on T2. Further testing in a larger study with information on blood flow levels would be required to confirm this.
一般认为,在T2加权磁共振成像(MRI)上显示异常的组织已发生梗死,且任何半暗带都位于T2可见病变之外。我们使用质子磁共振波谱成像研究梗死组织的分布情况。
对于急性半球缺血性卒中症状患者,在卒中发生后最多3天内进行成像,我们使用质子磁共振波谱成像,探究T2加权磁共振图像上异常(高信号)区域内及周围N-乙酰天门冬氨酸(NAA,完整神经元的标志物)的分布情况。
在11例卒中发作后24至72小时成像的患者中,T2图像上高信号边缘以外几乎没有受损神经元(NAA降低)的证据。然而,在T2异常区域内,T2上明显异常(非常高信号)的区域与仅轻微异常(轻微高信号)的区域之间,NAA含量(即完整神经元的比例)存在统计学显著差异。
T2可见病变的高信号范围和程度直接反映神经元损伤的程度;缺乏T2可见病变提示成像时神经元主要保持完整。我们推测,一旦组织损伤达到临界(可能不可逆)水平,T2图像会迅速变得异常,梗死的病理分期与其在T2上的显影之间没有明显的时间滞后。需要在一项更大规模的研究中进一步测试,结合血流水平信息来证实这一点。