Saur Dorothee, Buchert Ralph, Knab Rene, Weiller Cornelius, Röther Joachim
Department of Neurology, University Medical Center Freiburg, Breisacher Strasse 64, 79106 Freiburg, Germany.
Stroke. 2006 Nov;37(11):2713-9. doi: 10.1161/01.STR.0000244827.36393.8f. Epub 2006 Oct 5.
The mismatch of hypoperfused tissue on perfusion imaging and ischemic tissue on diffusion-weighted imaging is used as a surrogate marker for thrombolytic therapy in the extended time window. Mismatch tissue may recover completely, progress toward infarction, or proceed toward incomplete infarction with selective loss of cortical neurons. We used [(123)I]iomazenil-single-photon emission computed tomography (IMZ-SPECT) to characterize the neuronal integrity of reperfused "tissue at risk of infarction" that appeared morphologically intact on follow-up magnetic resonance imaging (MRI).
Twelve patients with acute stroke with striatocapsular (SC) infarctions were examined with multimodal MRI at days 0, 1, and 7; IMZ-SPECT was performed at days 5 to 15. The PI at day 0, fluid-attenuated inversion recovery (FLAIR) image at day 7, and IMZ-SPECT were coregistered and stereotactically normalized. The mismatch volume of interest (VOI) was defined as the initial PI lesion subtracted by the FLAIR lesion at day 7. An asymmetry ratio (AR) was computed by dividing the mean IMZ uptake of the mismatch VOI by the unaffected mirror VOI. The same AR was computed for signal intensity on FLAIR images at day 7. Three patients with cortical infarctions were included for calibration of the AR. In this group, the VOI consisted of the FLAIR lesion at day 7.
All patients with SC infarctions had a large mismatch of initially hypoperfused (112+/-31 mL; mean+/-SD) and finally infarcted tissue (19+/-14 mL). Mean AR of cortical IMZ uptake was 0.85+/-0.01 in cortical infarctions and 0.95+/-0.03 in SC infarctions; thereby AR showed a continuous distribution from clearly reduced (0.89) to normal (1.01) in SC infarctions. Mean AR for FLAIR signal intensity was 1.84+/-0.14 for cortical infarctions and normal (1.01+0.03) for SC infarctions.
IMZ-SPECT detected a selective loss of cortical neurons in patients with SC infarctions in transient hypoperfused tissue, which was morphologically intact on MRI.
灌注成像显示的灌注不足组织与扩散加权成像显示的缺血组织之间的不匹配,被用作延长时间窗内溶栓治疗的替代标志物。不匹配组织可能完全恢复、进展为梗死,或进展为伴有皮质神经元选择性丢失的不完全梗死。我们使用[(123)I]碘美托咪定单光子发射计算机断层扫描(IMZ-SPECT)来表征在随访磁共振成像(MRI)上形态学完整的再灌注“梗死风险组织”的神经元完整性。
12例患有纹状囊(SC)梗死的急性卒中患者在第0、1和7天接受多模态MRI检查;在第5至15天进行IMZ-SPECT检查。将第0天的灌注成像(PI)、第7天的液体衰减反转恢复(FLAIR)图像和IMZ-SPECT进行配准并立体定向归一化。不匹配感兴趣区(VOI)定义为第7天的FLAIR病变减去初始PI病变。不对称率(AR)通过将不匹配VOI的平均IMZ摄取量除以未受影响的镜像VOI来计算。对第7天FLAIR图像上的信号强度计算相同的AR。纳入3例皮质梗死患者以校准AR。在该组中,VOI由第7天的FLAIR病变组成。
所有SC梗死患者最初灌注不足的组织(112±31 mL;平均值±标准差)与最终梗死组织(19±14 mL)之间存在较大不匹配。皮质梗死中皮质IMZ摄取的平均AR为0.85±0.01,SC梗死中为0.95±0.03;因此,在SC梗死中,AR显示出从明显降低(0.89)到正常(1.01)的连续分布。皮质梗死中FLAIR信号强度的平均AR为1.84±0.14,SC梗死中为正常(1.01±0.03)。
IMZ-SPECT检测到SC梗死患者短暂灌注不足组织中皮质神经元的选择性丢失,该组织在MRI上形态学完整。