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跨人群理解大脑衰老:结构分析的综合框架

Understanding Brain Aging Across Populations: A Comprehensive Framework for Structural Analysis

Alphin J Thottupattu, Jayanthi Sivaswamy, Bharath Holla, Jithender Saini

AI总结:

本研究针对全球人口老龄化背景下不同种族人群大脑衰老结构差异问题,提出结合FSL-FAST组织分割与微分同胚变换连续模型的双路径分析框架,在四人群MRI数据集上验证,为全球跨人群脑衰老结构比较提供了开创性方法。

摘要:

在全球人口老龄化的背景下,理解不同人群间独特的神经衰老模式至关重要。本研究旨在揭示考虑不同种族背景的衰老大脑结构变异。研究采用双管齐下的方法,分析了来自印度、中国、日本和高加索人群的MRI数据。首先开展了群体分析,通过FSL-FAST(FSL的自动分割工具)进行组织分割,检测灰质(GM)、白质(WM)和脑脊液(CSF)。随后采用基于连续模型的分析,将衰老定义为一种微分同胚变换,这一方法支持详细的人群内和人群间分析,并检测了各人群相对于印度人群的整体解剖结构及年龄相关距离。研究获得了大脑变形随时间变化的空间分布的详细见解,尤其关注相对于参考时间点的解剖学变化。所提出的综合结构比较框架应用于包含四个不同人群的样本数据集,是在全球范围内比较大脑衰老相关结构差异的开创性工作。后续使用更大数据集、并基于不同标准在群体间应用该分析的研究,将进一步深化我们对衰老相关变化的理解。

英文摘要:

Understanding distinct neurological aging patterns across various populations is vital in the context of a globally aging populace. This study seeks to unravel the structural variations in the aging brain, taking into consideration different ethnic backgrounds. MRI data from Indian, Chinese, Japanese, and Caucasian populations were analyzed using a two-pronged approach. Initially, a group analysis was performed involving tissue segmentation through FSL-FAST, examining gray matter (GM), white matter (WM), and cerebrospinal fluid (CSF). Subsequently, a continuous model-based analysis was employed, defining aging as a diffeomorphic transformation, which facilitated a detailed intra- and inter-population analysis, and examined both global anatomy and age-dependent distances of each population in comparison to the Indian population. Detailed insights into the spatial distribution of brain deformations over time were obtained, with particular focus on anatomical changes relative to a reference time point. The proposed comprehensive structural comparison framework, applied to a sample dataset encompassing four distinct populations, represents a pioneering effort to compare structural differences related to brain aging on a global scale. Subsequent studies utilizing larger datasets and applying the proposed analysis across groups based on various criteria will further advance our understanding of aging-related changes.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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