Dallmeier Julian D, Meysami Somayeh, Merrill David A, Raji Cyrus A
1Department of Neuroscience, Center for Applied Medical Research (CIMA), University of Navarra, Pamplona, Spain.
2Neurology, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
Br J Radiol. 2019 Sep;92(1101):20180925. doi: 10.1259/bjr.20180925. Epub 2019 Jul 26.
Chronic traumatic encephalopathy (CTE) is a neurodegenerative disorder that is of epidemic proportions in contact sports athletes and is linked to subconcussive and concussive repetitive head impacts (RHI). Although postmortem analysis is currently the only confirmatory method to diagnose CTE, there has been progress in early detection techniques of fluid biomarkers as well as in advanced neuroimaging techniques. Specifically, promising new methods of diffusion MRI and radionucleotide PET scans could aid in the early detection of CTE.The authors examine early detection methods focusing on various neuroimaging techniques. Advances in structural and diffusion MRI have demonstrated the ability to measure volumetric and white matter abnormalities associated with CTE. Recent studies using radionucleotides such as flortaucipir and F-FDDNP have shown binding patterns that are consistent with the four stages of neurofibrillary tangle (NFT) distribution postmortem. Additional research undertakings focusing on fMRI, MR spectroscopy, susceptibility-weighted imaging, and singlephoton emission CT are also discussed as are advanced MRI methods such as diffusiontensor imaging and arterial spin labeled. Neuroimaging is fast becoming a key instrument in early detection and could prove essential for CTE quantification. This review explores a global approach to early detection.Limited data of CTE biomarkers with postmortem confirmation are available. While some data exist, they are limited by selection bias. It is unlikely that a single test will be sufficient to properly diagnosis and distinguish CTE from other neurodegenerative diseases such as Alzheimer disease or Frontotemporal Dementia. However, with a combination of fluid biomarkers, neuroimaging, and genetic testing, early detection may become possible.
慢性创伤性脑病(CTE)是一种神经退行性疾病,在接触性运动运动员中呈流行态势,与重复性轻度和中度头部撞击(RHI)有关。尽管目前尸检分析是诊断CTE的唯一确诊方法,但在液体生物标志物的早期检测技术以及先进的神经成像技术方面已经取得了进展。具体而言,扩散磁共振成像(MRI)和放射性核素正电子发射断层扫描(PET)扫描等有前景的新方法有助于CTE的早期检测。作者研究了侧重于各种神经成像技术的早期检测方法。结构和扩散MRI的进展已证明有能力测量与CTE相关的体积和白质异常。最近使用诸如氟替卡匹尔和F-FDDNP等放射性核素的研究显示出与死后神经原纤维缠结(NFT)分布的四个阶段一致的结合模式。还讨论了侧重于功能磁共振成像(fMRI)、磁共振波谱(MR spectroscopy)、磁敏感加权成像和单光子发射计算机断层扫描(single-photon emission CT)的其他研究项目,以及诸如扩散张量成像和动脉自旋标记等先进的MRI方法。神经成像正迅速成为早期检测的关键工具,可能对CTE定量至关重要。本综述探讨了早期检测的整体方法。有死后确认的CTE生物标志物的有限数据。虽然存在一些数据,但它们受到选择偏倚的限制。单一测试不太可能足以正确诊断CTE并将其与其他神经退行性疾病(如阿尔茨海默病或额颞叶痴呆)区分开来。然而,通过结合液体生物标志物、神经成像和基因检测,早期检测可能成为可能。