利用 7 特斯拉核磁共振成像描绘人体岛叶皮层内的活体 T1 加权强度轮廓

Connor Dalby, Austin Jon Dibble, Joana Carvalheiro, Filippo Queirazza, Michele Sevegnani, Monika Harvey, Michele Svanera, Alessio Fracasso
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摘要

在人类中,脑岛皮层在感觉和认知功能中扮演着不可或缺的角色,这一点已经得到了充分的证实,而在人类和非人灵长类动物体内,脑岛的精细解剖细节也得到了广泛的研究。然而,对人类脑岛解剖结构(总体而言)和半岛内分割(特别是)的体内研究却很有限。目前的研究利用 7 特斯拉磁共振成像技术来描绘人类皮层内的 T1 加权强度剖面,作为髓鞘化的间接代表。我们的分析显示,在整个岛叶皮层中,有两个相对较高和较低 T1 加权信号强度的独立集群,分别位于岛叶后部、前部和中部的三个不同皮层位置。后部和前部皮层位置的特征是 T1 加权信号强度升高,而在中间岛叶皮层位置观察到的信号强度较低,这与体外研究结果相符。重要的是,前部高 T1 加权群的检测取决于定义岛叶 ROI 时所选择的脑图谱。我们在两个不同地点(n1 = 21,英国格拉斯哥;n2 = 101,荷兰阿姆斯特丹)获得的两个独立队列中,在个体和群体水平上获得了可靠的体内半岛内解析。这些结果反映了对体内岛叶解剖结构的新认识,同时突出了 7 特斯拉在神经成像中的应用。具体而言,目前的研究还为在 7 特斯拉及以上的频率下研究半岛内的配位铺平了道路,并探讨了对个体化医疗方法的进一步影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Delineating In-Vivo T1-Weighted Intensity Profiles Within the Human Insula Cortex Using 7-Tesla MRI
The integral role of the insula cortex in sensory and cognitive function has been well documented in humans, and fine anatomical details characterising the insula have been extensively investigated ex-vivo in both human and non-human primates. However, in-vivo studies of insula anatomy in humans (in general), and within-insula parcellation (in particular) have been limited. The current study leverages 7 tesla magnetic resonance imaging to delineate T1-weighted intensity profiles within the human cortex, serving as an indirect proxy of myelination. Our analysis revealed two separate clusters of relatively high and low T1-weighted signal intensity across the insula cortex located in three distinct cortical locations within the posterior, anterior, and middle insula. The posterior and anterior cortical locations are characterised by elevated T1-weighted signal intensities, contrasting with lower intensity observed in the middle insular cortical location, compatible with ex-vivo studies. Importantly, the detection of the high T1-weighted anterior cluster is determined by the choice of brain atlas employed to define the insular ROI. We obtain reliable in-vivo within-insula parcellation at the individual and group levels, across two separate cohorts acquired in two separate sites (n1 = 21, Glasgow, UK; n2 = 101, Amsterdam, NL). These results reflect new insights into the insula anatomical structure, in-vivo, while highlighting the use of 7 tesla in neuroimaging. Specifically, the current study also paves the way to study within-insula parcellation at 7 tesla and above, and discusses further implications for individualised medicine approaches.
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