在 7 T 下对未固定的死后婴儿大脑进行高分辨率弥散成像

Wenchuan Wu, Sebastian W Rieger, L. Baxter, Eleri Adams, Jesper L. R. Andersson, Maria M. Cobo, Foteini Andritsou, Matteo Bastiani, Ria Evans Fry, Robert Frost, Sean Fitzgibbon, S. Foxley, Darren Fowler, Chris Gallagher, A. Howard, J. Hajnal, Fiona Moultrie, V. Monk, David A Porter, Daniel Papp, Anthony Price, J. Sallet, Michael Sanders, Dominic Wilkinson, Rebeccah Slater, Karla L. Miller
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摘要

摘要 婴儿大脑的弥散核磁共振成像可研究大脑发育过程中成熟纤维的组织结构。死后成像有可能通过使用长扫描时间来实现高分辨率,从而对小结构进行精确评估。死后弥散核磁共振成像的技术开发主要集中在对固定组织的扫描上,这种扫描方式不受温度漂移等影响,因为温度漂移会导致未固定组织退化。如果能够扫描完整身体中未固定的组织,就可以在不捐献器官的情况下进行死后研究,但这也带来了新的技术挑战。本文介绍了我们在新生儿发展中人类连接组项目(dHCP)背景下的扫描设置、方案优化和组织保护方法。一个主要的考虑因素是,鉴于超高磁场强度下的能量沉积,需要在扫描过程中保护未固定组织的完整性。我们展示了该研究首批招募的两名受试者之一的研究结果,该受试者于出生后第 46 天(月龄后 29+6 周)死亡,展示了高质量的弥散核磁共振成像数据。我们发现弥散特性的改变与之前报道的死后变化一致。初步的体素分析和束谱分析与年龄匹配的体内 dHCP 数据进行了比较。这些结果表明,可以通过获取未固定组织的高质量、高分辨率死后数据来探索发育中的人类大脑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-resolution diffusion imaging in the unfixed post-mortem infant brain at 7 T
Abstract Diffusion MRI of the infant brain allows investigation of the organizational structure of maturing fibers during brain development. Post-mortem imaging has the potential to achieve high resolution by using long scan times, enabling precise assessment of small structures. Technical development for post-mortem diffusion MRI has primarily focused on scanning of fixed tissue, which is robust to effects like temperature drift that can cause unfixed tissue to degrade. The ability to scan unfixed tissue in the intact body would enable post-mortem studies without organ donation, but poses new technical challenges. This paper describes our approach to scan setup, protocol optimization, and tissue protection in the context of the Developing Human Connectome Project (dHCP) of neonates. A major consideration was the need to preserve the integrity of unfixed tissue during scanning in light of energy deposition at ultra-high magnetic field strength. We present results from one of the first two subjects recruited to the study, who died on postnatal day 46 at 29+6 weeks postmenstrual age, demonstrating high-quality diffusion MRI data. We find altered diffusion properties consistent with post-mortem changes reported previously. Preliminary voxel-wise and tractography analyses are presented with comparison to age-matched in vivo dHCP data. These results show that high-quality, high-resolution post-mortem data of unfixed tissue can be acquired to explore the developing human brain.
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