神经影像学
DNA甲基化
生物标志物
组学
自编码
医学
疾病
认知
神经科学
限制
计算生物学
生物信息学
脑老化
大脑活动与冥想
人脑
生物标志物发现
脑病
判别式
基因组学
生物
甲基化
人工智能
认知功能衰退
发病年龄
脑组织
认知障碍
作者
Wenrui Cui,Hong Pang,Yi Yang,Muheng Shang,HongDong LI,Lei Du
标识
DOI:10.1109/bibm66473.2025.11356568
摘要
Brain age (BA) is recognized as a significant biomarker for health, closely associated with brain aging, and has been proposed to correlate with the progression of neurodegenerative diseases. Previous studies on brain age prediction predominantly relied on single omics data, limiting the integration of cooperative information from multiple omics data. Additionally, existing brain age prediction methods are susceptible to intermediate features since not all these features are related to brain age. To address these limitations, the study introduces a multiomics attention-based VAE method to predict brain age by integrating neuroimaging data and DNA methylation (DNAm) data, aiming to identify biologically meaningful features truly associated with brain aging. Experimental results show that our method predicts brain age with the MAE of 2.08 years, outperforming the state-of-the-art methods under the same experimental conditions. Furthermore, we estimated the brain age gap in patients with Mild Cognitive Impairment (MCI) and Alzheimer's Disease (AD). The results of both MCI and AD patients exhibited a larger brain age gap compared to the Cognitively Normal (CN) group, indicating the model's discriminative capacity across different diagnostic groups. These findings can assist in the early diagnosis of AD and the formulation of early treatment strategies.
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