Bray Signe
Departments of Radiology and Pediatrics, Cumming School of Medicine, University of Calgary, 2500 University Ave NW, Calgary AB, T2N1N4, Canada.
Child and Adolescent Imaging Research (CAIR) Program, 2888 Shaganappi Trail NW, Calgary, AB, T3B 6A8, Canada.
Hum Brain Mapp. 2017 May;38(5):2398-2407. doi: 10.1002/hbm.23526. Epub 2017 Jan 24.
Healthy brain development involves changes in brain structure and function that are believed to support cognitive maturation. However, understanding how structural changes such as grey matter thinning relate to functional changes is challenging. To gain insight into structure-function relationships in development, the present study took a data driven approach to define age-related patterns of variation in gray matter volume (GMV), cerebral blood flow (CBF) and blood-oxygen level dependent (BOLD) signal variation (fractional amplitude of low-frequency fluctuations; fALFF) in 59 healthy children aged 7-18 years, and examined relationships between modalities. Principal components analysis (PCA) was applied to each modality in parallel, and participant scores for the top components were assessed for age associations. We found that decompositions of CBF, GMV and fALFF all included components for which scores were significantly associated with age. The dominant patterns in GMV and CBF showed significant (GMV) or trend level (CBF) associations with age and a strong spatial overlap, driven by increased signal intensity in default mode network (DMN) regions. GMV, CBF and fALFF additionally showed components accounting for 3-5% of variability with significant age associations. However, these patterns were relatively spatially independent, with small-to-moderate overlap between modalities. Independence of age effects was further demonstrated by correlating individual subject maps between modalities: CBF was significantly less correlated with GMV and fALFF in older children relative to younger. These spatially independent effects of age suggest that the parallel decline observed in global GMV and CBF may not reflect spatially synchronized processes. Hum Brain Mapp 38:2398-2407, 2017. © 2017 Wiley Periodicals, Inc.
健康的大脑发育涉及大脑结构和功能的变化,这些变化被认为有助于认知成熟。然而,理解诸如灰质变薄等结构变化与功能变化之间的关系具有挑战性。为了深入了解发育过程中的结构-功能关系,本研究采用数据驱动的方法来定义59名7至18岁健康儿童的灰质体积(GMV)、脑血流量(CBF)和血氧水平依赖(BOLD)信号变化(低频波动分数振幅;fALFF)的年龄相关变化模式,并检查各模态之间的关系。主成分分析(PCA)并行应用于每个模态,并评估顶级成分的参与者分数与年龄的关联。我们发现,CBF、GMV和fALFF的分解都包括与年龄显著相关的成分。GMV和CBF的主要模式显示出与年龄的显著(GMV)或趋势水平(CBF)关联以及强烈的空间重叠,这是由默认模式网络(DMN)区域信号强度增加驱动的。GMV、CBF和fALFF还显示出占变异性3 - 5%且与年龄有显著关联的成分。然而,这些模式在空间上相对独立,各模态之间的重叠较小到中等。通过关联各模态之间的个体受试者图谱进一步证明了年龄效应的独立性:与年幼儿童相比,年龄较大儿童的CBF与GMV和fALFF的相关性显著降低。这些年龄的空间独立效应表明,在全球GMV和CBF中观察到的平行下降可能并不反映空间同步过程。《人类大脑图谱》38:2398 - 2407,2017年。© 2017威利期刊公司。