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首页> 外文期刊>NeuroImage >An unbiased data-driven age-related structural brain parcellation for the identification of intrinsic brain volume changes over the adult lifespan
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An unbiased data-driven age-related structural brain parcellation for the identification of intrinsic brain volume changes over the adult lifespan

机译:无偏见的数据驱动年龄相关的结构脑局,用于鉴定成人寿命的内在脑体积变化

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This study aims to elucidate age-related intrinsic brain volume changes over the adult lifespan using an unbiased data-driven structural brain parcellation. Anatomical brain images from a cohort of 293 healthy volunteers ranging in age from 21 to 86 years were analyzed using independent component analysis (ICA). ICA-based parcellation identified 192 component images, of which 174 (90.6%) showed a significant negative correlation with age and with some components being more vulnerable to aging effects than others. Seven components demonstrated a convex slope with aging; 3 components had an inverted U-shaped trajectory, and 4 had a U-shaped trajectory. Linear combination of 86 components provided reliable prediction of chronological age with a mean absolute prediction error of approximately 7.2 years. Structural co-variation analysis showed strong interhemispheric, short-distance positive correlations and long-distance, inter-lobar negative correlations. Estimated network measures either exhibited a U-or an inverted U-shaped relationship with age, with the vertex occurring at approximately 45-50 years. Overall, these findings could contribute to our knowledge about healthy brain aging and could help provide a framework to distinguish the normal aging processes from that associated with age-related neurodegenerative diseases.
机译:本研究旨在使用无偏的数据驱动的结构脑局阐明成人寿命的年龄相关的内在脑体积。使用独立的分量分析(ICA)分析来自293岁的健康志愿者的群组的解剖学脑图像从21至86岁分析。基于ICA的局部鉴定了192个组分图像,其中174个成分图像(90.6%)显示出与年龄的显着的负相关性,并且一些组件比其他成分更容易受到老化的效果。七个组件展示了凸起的老化坡度; 3个部件具有倒U形轨迹,4个具有U形轨迹。线性组合为86个组分提供了对时间年龄的可靠预测,其平均绝对预测误差约为7.2岁。结构共变分析显示出强大的互撞性,短距离正相关性和长距离,间距间的负相关性。估计的网络措施要么与年龄的年龄呈现U型或倒U形关系,顶点在大约45-50岁时发生。总体而言,这些发现可能有助于我们对健康脑老化的知识,并有助于提供一个框架,以区分正常老化过程与年龄相关的神经变性疾病相关的正常老化过程。

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