Darekar Gauri, Murad Taslim, Miao Hui-Yuan, Thakuri Deepa S, Chand Ganesh B
Department of Radiology, Mallinckrodt Institute of Radiology, Washington University School of Medicine, St Louis, MO, 63110, United States.
Institute for Informatics, Data Science and Biostatistics, Washington University School of Medicine, St Louis, MO, 63110, United States.
Biol Methods Protoc. 2025 Aug 7;10(1):bpaf051. doi: 10.1093/biomethods/bpaf051. eCollection 2025.
Age is a significant risk factor for mild cognitive impairment (MCI) and Alzheimer's disease (AD) and identifying brain age patterns is critical for comprehending the normal aging and MCI/AD processes. Prior studies have widely established the univariate relationships between brain regions and age, while multivariate associations remain largely unexplored. Herein, various artificial intelligence (AI) models were used to perform brain age prediction using an MRI dataset ( = 825). The optimal AI model was then integrated with the feature importance methods, namely Shapley additive explanations (SHAP), local interpretable model-agnostic explanations, and layer-wise relevance propagation, to identify the significant multivariate brain regions hierarchically involved in this prediction. Our results showed that the deep learning model (referred to as AgeNet) outperformed conventional machine learning models for brain age prediction, and that AgeNet integrated with SHAP (referred to as AgeNet-SHAP) identified all ground-truth perturbed regions as key predictors of brain age in semi-simulation, demonstrating the validity of our methodology. In the experimental dataset, when compared to cognitively normal (CN) participants, MCI exhibited moderate differences in brain regions, whereas AD showed highly robust and widely distributed regional differences. Individualized AgeNet-SHAP regional features further showed associations with clinical severity scores in the AD continuum. These results collectively facilitate data-driven explainable AI approaches for disease progression, diagnostics, prognostics, and personalized medicine efforts.
年龄是轻度认知障碍(MCI)和阿尔茨海默病(AD)的一个重要风险因素,识别脑年龄模式对于理解正常衰老以及MCI/AD进程至关重要。先前的研究广泛确立了脑区与年龄之间的单变量关系,而多变量关联在很大程度上仍未得到探索。在此,使用各种人工智能(AI)模型,利用一个MRI数据集(n = 825)进行脑年龄预测。然后,将最优的AI模型与特征重要性方法,即夏普利值加法解释(SHAP)、局部可解释模型无关解释和逐层相关性传播相结合,以分层识别参与该预测的重要多变量脑区。我们的结果表明,深度学习模型(称为AgeNet)在脑年龄预测方面优于传统机器学习模型,并且与SHAP相结合的AgeNet(称为AgeNet-SHAP)在半模拟中识别出所有真实扰动区域作为脑年龄的关键预测因子,证明了我们方法的有效性。在实验数据集中,与认知正常(CN)参与者相比,MCI在脑区表现出中度差异,而AD则表现出高度稳健且广泛分布的区域差异。个性化的AgeNet-SHAP区域特征进一步显示与AD连续体中的临床严重程度评分相关。这些结果共同促进了用于疾病进展、诊断、预后和个性化医疗的基于数据驱动的可解释AI方法。