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arXiv 2604.22018q-bio.NCcs.AIcs.LGeess.SP

用于从动态功能连接中发现神经疾病稳健生物标记物的基础模型

Foundation models for discovering robust biomarkers of neurological disorders from dynamic functional connectivity

College of Computing and Data Science, Nanyang Technological University, Singapore(南洋理工大学计算与数据科学学院,新加坡);Department of Biomedical Engineering and the School of Artificial Intelligence and Data Engineering, Indian Institute of Technology Ropar, India(印度理工学院罗帕尔分校生物医学工程系和人工智能与数据工程学院);College of Instrument and Computer Science, Zhejiang University, China(浙江大学仪器与计算机科学学院)

Deepank Girish, Yi Hao Chan, Sukrit Gupta, Jing Xia, Jagath C. Rajapakse

AI总结:

本文提出RE-CONFIRM框架,评估深度学习模型中潜在生物标记物的稳健性,发现传统指标不足,提出Hub-LoRA技术提升模型性能并产生神经生物学忠实的生物标记物。

摘要:

近年来,几种脑基础模型(FM)已被提出,通过建模动态功能连接(FC)来预测脑疾病。尽管它们展示了出色的模型性能和零或少样本泛化能力,但识别出的潜在生物标记物特征尚未得到充分评估。我们提出RE-CONFIRM框架,用于评估由深度学习(DL)模型包括FM揭示的潜在生物标记物的稳健性。在五个大型自闭症谱系障碍(ASD)、注意缺陷多动障碍(ADHD)和阿尔茨海默病(AD)数据集上的实验发现,尽管常用性能指标能提供对模型预测的直观评估,但不足以评估这些模型识别出的生物标记物的稳健性。RE-CONFIRM指标揭示,简单微调FM会导致模型无法有效捕捉区域枢纽,即使在枢纽已知参与的疾病如ASD和ADHD中也是如此。为此,我们提出Hub-LoRA(低秩适应)作为微调技术,使FM不仅超越定制DL模型,还能产生由元分析支持的神经生物学忠实的生物标记物。RE-CONFIRM具有通用性,可轻松应用于确认基于功能磁共振成像数据集训练的DL模型的稳健性。代码可在:https://github.com/SCSE-Biomedical-Computing-Group/RE-CONFIRM获取。

英文摘要:

Several brain foundation models (FM) have recently been proposed to predict brain disorders by modelling dynamic functional connectivity (FC). While they demonstrate remarkable model performance and zero- or few-shot generalization, the salient features identified as potential biomarkers are yet to be thoroughly evaluated. We propose RE-CONFIRM, a framework for evaluating the robustness of potential biomarker candidates elucidated by deep learning (DL) models including FMs. From experiments on five large datasets of Autism Spectrum Disorder (ASD), Attention-deficit Hyperactivity Disorder (ADHD), and Alzheimer's Disease (AD), we found that although commonly used performance metrics provide an intuitive assessment of model predictions, they are insufficient for evaluating the robustness of biomarkers identified by these models. RE-CONFIRM metrics revealed that simply finetuning FMs leads to models that fail to capture regional hubs effectively, even in disorders where hubs are known to be implicated, such as ASD and ADHD. In view of this, we propose Hub-LoRA (Low-Rank Adaptation) as a fine-tuning technique that enables FMs to not only outperform customised DL models but also produce neurobiologically faithful biomarkers supported by meta-analyses. RE-CONFIRM is generalizable and can be easily applied to ascertain the robustness of DL models trained on functional MRI datasets. Code is available at: https://github.com/SCSE-Biomedical-Computing-Group/RE-CONFIRM.

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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