Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Charlestown, MA, USA; Harvard Medical School, Boston, MA, USA.
Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Charlestown, MA, USA; Harvard Medical School, Boston, MA, USA.
Neuroimage. 2019 May 1;191:325-336. doi: 10.1016/j.neuroimage.2019.02.036. Epub 2019 Feb 18.
Cerebral white matter exhibits age-related degenerative changes during the course of normal aging, including decreases in axon density and alterations in axonal structure. Noninvasive approaches to measure these microstructural alterations throughout the lifespan would be invaluable for understanding the substrate and regional variability of age-related white matter degeneration. Recent advances in diffusion magnetic resonance imaging (MRI) have leveraged high gradient strengths to increase sensitivity toward axonal size and density in the living human brain. Here, we examined the relationship between age and indices of axon diameter and packing density using high-gradient strength diffusion MRI in 36 healthy adults (aged 22-72) in well-defined central white matter tracts in the brain. A recently validated method for inferring the effective axonal compartment size and packing density from diffusion MRI measurements acquired with 300 mT/m maximum gradient strength was applied to the in vivo human brain to obtain indices of axon diameter and density in the corpus callosum, its sub-regions, and adjacent anterior and posterior fibers in the forceps minor and forceps major. The relationships between the axonal metrics, corpus callosum area and regional gray matter volume were also explored. Results revealed a significant increase in axon diameter index with advancing age in the whole corpus callosum. Similar analyses in sub-regions of the corpus callosum showed that age-related alterations in axon diameter index and axon density were most pronounced in the genu of the corpus callosum and relatively absent in the splenium, in keeping with findings from previous histological studies. The significance of these correlations was mirrored in the forceps minor and forceps major, consistent with previously reported decreases in FA in the forceps minor but not in the forceps major with age. Alterations in the axonal imaging metrics paralleled decreases in corpus callosum area and regional gray matter volume with age. Among older adults, results from cognitive testing suggested an association between larger effective compartment size in the corpus callosum, particularly within the genu of the corpus callosum, and lower scores on the Montreal Cognitive Assessment, largely driven by deficits in short-term memory. The current study suggests that high-gradient diffusion MRI may be sensitive to the axonal substrate of age-related white matter degeneration reflected in traditional DTI metrics and provides further evidence for regionally selective alterations in white matter microstructure with advancing age.
脑白质在正常衰老过程中会发生与年龄相关的退行性变化,包括轴突密度的降低和轴突结构的改变。非侵入性方法来测量这些微观结构变化贯穿整个生命周期将是非常宝贵的,有助于理解与年龄相关的白质退行性变的基质和区域变异性。扩散磁共振成像(MRI)的最新进展利用高梯度强度来提高活体人脑中轴突大小和密度的灵敏度。在这里,我们使用高梯度强度扩散 MRI 检查了 36 名健康成年人(年龄 22-72 岁)大脑中明确界定的中央白质束中年龄与轴突直径和密度指数之间的关系。最近验证的方法用于从具有 300 mT/m 最大梯度强度的扩散 MRI 测量中推断有效轴突隔室大小和包装密度,并将其应用于活体人脑,以获得胼胝体及其亚区的轴突直径和密度指数以及小钳和大钳的前后纤维。还探讨了轴突指标与胼胝体面积和区域灰质体积之间的关系。结果显示,整个胼胝体的轴突直径指数随年龄的增长而显著增加。胼胝体亚区的类似分析表明,与年龄相关的轴突直径指数和轴突密度变化在胼胝体的膝部最为明显,而在压部则相对不存在,与先前的组织学研究结果一致。这些相关性的意义在小钳和大钳中得到了反映,与先前报道的随年龄增长在小钳中 FA 降低但在大钳中没有降低的结果一致。轴突成像指标的变化与胼胝体面积和区域灰质体积随年龄的减少相平行。在老年人中,认知测试的结果表明,胼胝体中特别是在胼胝体的膝部的有效隔室大小较大与蒙特利尔认知评估的较低分数之间存在关联,这主要是由于短期记忆缺陷所致。本研究表明,高梯度扩散 MRI 可能对白质与年龄相关的退行性变的轴突基质敏感,这反映在传统的 DTI 指标中,并为随年龄增长白质微观结构的区域选择性改变提供了进一步证据。