正电子发射断层成像中枢神经系统脱髓鞘和再髓鞘。

Benedetta Bodini, Bruno Stankoff
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引用次数: 8

摘要

正电子发射断层扫描(PET)是一种基于注射放射性示踪剂的成像技术,该技术针对脑组织内的特定生物靶点,是一种特殊而敏感的技术,为量化中枢神经系统中的髓磷脂动力学提供了独特的机会。一些苯乙烯和苯并噻唑衍生物已被重新用于PET成像髓磷脂。在脱髓鞘和髓鞘异常模型中,选定的放射性示踪剂被证明可以可靠地量化脱髓鞘和髓鞘再生,从而允许在人类中进行转化。一项使用PET和最有效的苯并噻唑衍生物[11C]PIB对复发性多发性硬化症患者进行的初步研究支持了这样的假设,即该技术能够量化多发性硬化症(MS)病变中的髓磷脂含量,并随着时间的推移捕捉动态脱髓鞘和再髓鞘形成。这项研究首次在体内强调了骨髓鞘再生的个体特征对疾病病程的预后价值。未来,由于新型髓磷脂氟化示踪剂的出现,以及无创定量程序的建立和强大的PET- mr系统的使用,髓磷脂PET的临床应用将得到进一步推进。这将有助于解决关于髓鞘再生发病机制的体内关键未解问题,并在早期治疗试验中衡量新兴的髓鞘再生药物的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Imaging Central Nervous System Demyelination and Remyelination by Positron-Emission Tomography.

Positron Emission Tomography (PET), an imaging technique based on the injection of radiotracers directed against specific biological targets within brain tissues, within brain tissues, is a specific and sensitive technique which offers the unique opportunity to quantify myelin dynamics in the central nervous system. Several stilbene and benzothiazole derivatives have been repurposed to image myelin by PET. In demyelinating and dysmyelinating models, selected radiotracers were shown to reliably quantify demyelination and remyelination, allowing a translational approach in humans. A pilot study in subjects with active relapsing MS using PET and the most available benzothiazole derivative, [11C]PIB, supported the hypothesis that this technique is able to quantify myelin content in multiple sclerosis (MS) lesions and to capture dynamic demyelination and remyelination over time. This study highlighted for the first time in vivo the prognostic value of individual profiles of remyelination on the disease course. In future, the clinical application of myelin PET will be pushed forward thanks to the availability of novel fluorinated tracers for myelin, together with the setting up of non invasive quantification procedures and the use of powerful PET-MR systems. This will enable to address in vivo critical unanswered questions about the pathogenesis of remyelination, and to measure the efficacy of emerging promyelinating drugs in early-phase therapeutic trials.

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