人类皮层的高分辨率扩散张量成像揭示了健康寿命中的非线性轨迹。

Imaging neuroscience (Cambridge, Mass.) Pub Date : 2025-08-20 eCollection Date: 2025-01-01 DOI:10.1162/IMAG.a.115
J Alejandro Acosta-Franco, Graham Little, Christian Beaulieu
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引用次数: 0

摘要

人类皮层在整个生命周期中经历了显著的宏观结构和微观结构变化,这可以通过高分辨率扩散张量成像(DTI)来评估。在健康个体中,弥散在皮层表面的垂直方向更大,与神经元体和根尖树突对齐。本研究检测了190名健康个体(5-74岁)的DTI指标,以表征神经发育和衰老过程中规范的皮层变化。全脑DTI数据以1.5 mm各向同性分辨率获得,3T时仅需3:36分钟即可获得1000 s/mm²的b值。仅对扩散图像进行皮质分割,以获得总皮质和五个脑叶的厚度、径向性、分数各向异性(FA)、平均(MD)、轴向(AD)和径向扩散率(RD),并与年龄进行比较。皮层厚度呈指数下降,这与扩散度量横截面年龄轨迹不同。FA、MD、AD和RD呈u型轨迹,在成年期(~20-40岁)达到最小值。相比之下,辐射量呈立方型,儿童期下降,20-55岁稳定,55岁后再次下降,早期变化最大的是颞叶和枕叶,晚年下降的是额叶和顶叶。儿童期较大的DTI变化可能反映了切向纤维髓鞘形成的增加,以及神经元轴突、体细胞和树突的生长,而老年的变化可能表明细胞体密度和半径的减少。这项研究为未来研究神经发育和神经退行性疾病提供了基础。
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 tensor imaging of the human cortex reveals non-linear trajectories over the healthy lifespan.

The human cortex undergoes significant macrostructural and microstructural changes across the lifespan, which can be assessed using high-resolution diffusion tensor imaging (DTI). In healthy individuals, diffusion is typically greater perpendicular to the cortical surface, aligning with neuronal bodies and apical dendrites. This study examined DTI metrics in 190 healthy individuals (ages 5-74 years) to characterize normative cortical changes across neurodevelopment and aging. Whole-brain DTI data were acquired with 1.5 mm isotropic resolution and a b-value of 1000 s/mm² acquired in only 3:36 minutes at 3T. Cortical segmentation was performed exclusively on diffusion images to yield thickness, radiality, fractional anisotropy (FA), mean (MD), axial (AD), and radial diffusivity (RD) in total cortex as well as five lobes and were compared versus age. Cortical thickness decreased exponentially which differed from the diffusion metric cross-sectional age trajectories. FA, MD, AD, and RD exhibited u-shaped trajectories reaching minimum values in adulthood (~20-40 years). In contrast, radiality showed a cubic pattern, declining in childhood, stabilizing from 20-55 years, then decreasing again after 55, with the largest early-life changes in the temporal and occipital lobes and later-life declines in the frontal and parietal lobes. Steeper childhood DTI changes may reflect increased myelination of tangential fibers, as well as the growth of neuronal axons, somata, and dendrites, while elderly changes likely indicate reduced cell body density and radius. This study provides a baseline for future research into neurodevelopment and neurodegenerative diseases across the lifespan.

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