通过表面积建模实现脑区精细化年龄预测,提升临床可解释性。
SurfAge-Net: A Hierarchical Surface-Based Network for Interpretable Fine-Grained Brain Age Prediction
- 基于脑表面多形态指标,捕捉局部发育模式
- 区域平均误差0.45周,优于现有方法
- 适合神经发育异常早期筛查与机制研究
脑年龄预测是评估脑健康状态、检测神经发育及神经退行性疾病偏差的重要工具。然而,现有方法多聚焦全脑预测,忽视了脑成熟过程中的显著区域异质性,难以发现局部异常轨迹。为此,本文提出一种新型球面表面对应的脑年龄预测网络(SurfAge-Net),融合多种形态度量,增强鲁棒性与临床可解释性。SurfAge-Net引入皮层组织的连接组学原则,通过空间-通道混合机制与侧化感知注意力,显式建模脑区内部及双半球间依赖关系,精准刻画各目标区域特有的协调成熟模式。在三个胎儿及新生儿数据集上验证,SurfAge-Net表现优异(全局平均绝对误差MAE=0.54周,区域MAE=0.45周,单位为孕周/产后周),并在外部队列中展现出强泛化能力。该模型生成空间精确、生物可解释的皮层成熟图谱,有效识别异常发育群体中的异质性延迟与区域特异性异常。结果表明,细粒度脑年龄预测为推进神经发育研究和早期临床评估提供了新范式。
原文摘要 · Abstract (English)
Brain age prediction serves as a powerful framework for assessing brain status and detecting deviations associated with neurodevelopmental and neurodegenerative disorders. However, most existing approaches emphasize whole-brain age prediction and therefore overlook the pronounced regional heterogeneity of brain maturation that is crucial for detecting localized atypical trajectories. To address this limitation, we propose a novel spherical surface-based brain age prediction network (SurfAge-Net) that leverages multiple morphological metrics to capture region-specific developmental patterns with enhanced robustness and clinical interpretability. SurfAge-Net establishes a new modeling paradigm by incorporating the connectomic principles of cortical organization: it explicitly models both intra- and inter-hemispheric dependencies through a spatial-channel mixing and a lateralization-aware attention mechanism, enabling the network to characterize the coordinate maturation pattern uniquely associated with each target region. Validated on three fetal and neonatal datasets, SurfAge-Net outperforms existing approaches (global MAE = 0.54, regional MAE = 0.45 in gestational/postmenstrual weeks) and demonstrates strong generalizability across external cohorts. Importantly, it provides spatially precise and biologically interpretable maps of cortical maturation, effectively identifying heterogeneous delays and regional-specific abnormalities in atypical developmental populations. These results established fine-grained brain age prediction as a promising paradigm for advancing neurodevelopmental research and supporting early clinical assessment.
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