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本文引用的文献

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Multishell diffusion imaging reveals sex-specific trajectories of early white matter degeneration in normal aging.多壳弥散成像揭示了正常衰老过程中早期白质退化的性别特异性轨迹。
Neurobiol Aging. 2020 Feb;86:191-200. doi: 10.1016/j.neurobiolaging.2019.11.014. Epub 2019 Nov 27.
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MRtrix3: A fast, flexible and open software framework for medical image processing and visualisation.MRtrix3:一个用于医学图像处理和可视化的快速、灵活、开放的软件框架。
Neuroimage. 2019 Nov 15;202:116137. doi: 10.1016/j.neuroimage.2019.116137. Epub 2019 Aug 29.
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Spatial gradients of healthy aging: a study of myelin-sensitive maps.健康老龄化的空间梯度:髓鞘敏感图谱研究。
Neurobiol Aging. 2019 Jul;79:83-92. doi: 10.1016/j.neurobiolaging.2019.03.002. Epub 2019 Mar 12.
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Michigan Neural Distinctiveness (MiND) study protocol: investigating the scope, causes, and consequences of age-related neural dedifferentiation.密歇根神经独特性(MiND)研究方案:探究与年龄相关的神经去分化的范围、成因及后果。
BMC Neurol. 2019 Apr 12;19(1):61. doi: 10.1186/s12883-019-1294-6.
5
Connectivity-enhanced diffusion analysis reveals white matter density disruptions in first episode and chronic schizophrenia.连接增强扩散分析揭示首发和慢性精神分裂症患者的白质密度紊乱。
Neuroimage Clin. 2018 Feb 22;18:608-616. doi: 10.1016/j.nicl.2018.02.015. eCollection 2018.
6
Improvement in White Matter Tract Reconstruction with Constrained Spherical Deconvolution and Track Density Mapping in Low Angular Resolution Data: A Pediatric Study and Literature Review.低角分辨率数据中基于约束球形反卷积和轨迹密度映射的白质纤维束重建改进:一项儿科研究及文献综述
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7
Investigating white matter fibre density and morphology using fixel-based analysis.使用基于固定点的分析方法研究白质纤维密度和形态。
Neuroimage. 2017 Jan 1;144(Pt A):58-73. doi: 10.1016/j.neuroimage.2016.09.029. Epub 2016 Sep 14.
8
White Matter Microstructural Organization Is Higher with Age in Adult Superior Cerebellar Peduncles.成人上小脑脚的白质微结构组织随年龄增长而更复杂。
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9
White matter and memory in healthy adults: Coupled changes over two years.健康成年人的白质与记忆:两年间的耦合变化
Neuroimage. 2016 May 1;131:193-204. doi: 10.1016/j.neuroimage.2015.10.085. Epub 2015 Nov 3.
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Differential aging of cerebral white matter in middle-aged and older adults: A seven-year follow-up.中老年人脑白质的差异老化:一项七年随访研究
Neuroimage. 2016 Jan 15;125:74-83. doi: 10.1016/j.neuroimage.2015.10.030. Epub 2015 Oct 19.

年龄相关的白质差异:使用基于体素的分析理解张量结果。

Age-Related Differences in White Matter: Understanding Tensor-Based Results Using Fixel-Based Analysis.

机构信息

Department of Psychology, University of Michigan, Ann Arbor, MI 48109, USA.

Department of Epidemiology and Biostatistics, Michigan State University, East Lansing, MI 48824, USA.

出版信息

Cereb Cortex. 2021 Jul 5;31(8):3881-3898. doi: 10.1093/cercor/bhab056.

DOI:10.1093/cercor/bhab056
PMID:33791797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8440891/
Abstract

Aging is associated with widespread alterations in cerebral white matter (WM). Most prior studies of age differences in WM have used diffusion tensor imaging (DTI), but typical DTI metrics (e.g., fractional anisotropy; FA) can reflect multiple neurobiological features, making interpretation challenging. Here, we used fixel-based analysis (FBA) to investigate age-related WM differences observed using DTI in a sample of 45 older and 25 younger healthy adults. Age-related FA differences were widespread but were strongly associated with differences in multi-fiber complexity (CX), suggesting that they reflected differences in crossing fibers in addition to structural differences in individual fiber segments. FBA also revealed a frontolimbic locus of age-related effects and provided insights into distinct microstructural changes underlying them. Specifically, age differences in fiber density were prominent in fornix, bilateral anterior internal capsule, forceps minor, body of the corpus callosum, and corticospinal tract, while age differences in fiber cross section were largest in cingulum bundle and forceps minor. These results provide novel insights into specific structural differences underlying major WM differences associated with aging.

摘要

衰老是与脑白质(WM)广泛改变相关的。大多数关于 WM 年龄差异的先前研究都使用了弥散张量成像(DTI),但典型的 DTI 指标(例如分数各向异性;FA)可以反映多种神经生物学特征,这使得解释变得具有挑战性。在这里,我们使用基于固定点的分析(FBA)来研究在使用 DTI 的 45 名老年人和 25 名年轻健康成年人样本中观察到的与年龄相关的 WM 差异。与年龄相关的 FA 差异广泛存在,但与多纤维复杂性(CX)的差异密切相关,这表明它们反映了交叉纤维的差异,而不仅仅是单个纤维段的结构差异。FBA 还揭示了与年龄相关的额叶边缘效应的位置,并提供了对其潜在的不同微观结构变化的深入了解。具体而言,穹窿、双侧内囊前肢、小内囊脚、胼胝体体部和皮质脊髓束中的纤维密度差异在年龄上较为显著,而在扣带束和小内囊脚中的纤维横截面积差异在年龄上最大。这些结果为与衰老相关的主要 WM 差异的基础上的具体结构差异提供了新的见解。