Nuclear Medicine and PET Center, Hyogo College of Medicine, 1-1 Mukogawa, Nishinomiya, Japan.
Ann Nucl Med. 2010 Nov;24(9):629-38. doi: 10.1007/s12149-010-0421-7. Epub 2010 Oct 16.
Neuroimaging in ischemic stroke continues to be one of the most developing fields in nuclear medicine. Many studies have established the efficacy of blood flow and metabolism measurements in acute ischemic stroke. Although the release of recombinant tissue plasminogen activator in clinical practice has minimized the use of SPECT or PET in the first few hours of ischemic stroke onset, implementing these techniques into a set of initial examinations is still beneficial to exclude risky patients for reperfusion therapy beyond several hours after onset. Rescuing of viable tissue suffering ischemic penumbra is an important target of early therapeutic strategy. Ischemic penumbra can be visualized by means of perfusion imaging, central type benzodiazepine receptor imaging, and hypoxy imaging. In the later phase of subacute ischemic stroke, inflammation and apoptosis can be visualized by means of peripheral-type benzodiazepine receptor imaging and annexin V imaging, respectively. Imaging of the penumbra and cellular responses will help evaluate the effects of drugs and interventions for ischemic stroke, suggesting its potential as a marker of the efficacy of future therapeutic regimens.
神经影像学在缺血性卒中领域一直是核医学中发展最为迅速的领域之一。许多研究已经证实了血流和代谢测量在急性缺血性卒中中的有效性。尽管在临床实践中使用重组组织型纤溶酶原激活剂已最大限度地减少了 SPECT 或 PET 在缺血性卒中超急性期的应用,但将这些技术纳入一组初始检查中对于排除发病数小时后进行再灌注治疗的风险患者仍然是有益的。挽救处于缺血半暗带的存活组织是早期治疗策略的一个重要目标。可以通过灌注成像、中央型苯二氮䓬受体成像和缺氧成像来显示缺血半暗带。在亚急性缺血性卒中的后期,可以通过外周型苯二氮䓬受体成像和膜联蛋白 V 成像分别显示炎症和细胞凋亡。半暗带和细胞反应的成像将有助于评估缺血性卒中药物和干预措施的效果,提示其作为未来治疗方案疗效标志物的潜力。