DAPNet:结合疾病临床和分子关联的多视图对比网络,用于疾病进展预测。

IF 3.3 3区 医学 Q2 MEDICAL INFORMATICS
Haoyu Tian, Xiong He, Kuo Yang, Xinyu Dai, Yiming Liu, Fengjin Zhang, Zixin Shu, Qiguang Zheng, Shihua Wang, Jianan Xia, Tiancai Wen, Baoyan Liu, Jian Yu, Xuezhong Zhou
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引用次数: 0

摘要

背景:及时准确地预测疾病进展对于促进各种慢性疾病的早期干预和治疗至关重要。然而,由于疾病进展的复杂性和纵向性,训练深度学习模型所需的临床数据的容量和完整性仍然是一个重大挑战。本研究旨在探索一种新方法,既能降低数据依赖性,又能达到与现有研究相当的预测性能:本研究提出了基于深度学习的疾病进展预测模型 DAPNet,该模型仅利用合并症持续时间(不依赖多模态数据或全面的医疗记录)和生物医学知识图谱中的疾病关联来提供高性能预测。DAPNet 首次将多视图对比学习应用于疾病进展预测任务。与其他有关合并症的研究相比,DAPNet 创新性地整合了分子水平的疾病关联信息,结合了疾病共现和 ICD10,充分挖掘了疾病之间的关联;结果:本研究使用了一个去标识化的临床数据集对 DAPNet 进行了验证,该数据集来自医疗索赔,包括 2714 名患者和 10856 次就诊。同时,还构建了基于 MIMIC-IV 的肾脏数据集(606 名患者),以充分验证其性能。结果表明,DAPNet 在重症肺炎数据集上取得了最先进的性能(F1=0.84,提高了 8.7%),在肾病数据集上的表现优于六个基线模型(F1=0.80,提高了 21.3%)。通过病例分析,我们阐明了DAPNet模型确定的临床和分子关联,这有助于更好地理解和解释潜在的疾病关联,从而为模型提供了可解释性:所提出的 DAPNet 首次利用了合并症持续时间和疾病关联网络,在多视图对比学习的基础上实现了更准确的疾病进展预测,为患者的早期诊断和治疗提供了有价值的见解。基于疾病关联网络,我们的研究增强了疾病进展预测的可解释性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DAPNet: multi-view graph contrastive network incorporating disease clinical and molecular associations for disease progression prediction.

Background: Timely and accurate prediction of disease progress is crucial for facilitating early intervention and treatment for various chronic diseases. However, due to the complicated and longitudinal nature of disease progression, the capacity and completeness of clinical data required for training deep learning models remains a significant challenge. This study aims to explore a new method that reduces data dependency and achieves predictive performance comparable to existing research.

Methods: This study proposed DAPNet, a deep learning-based disease progression prediction model that solely utilizes the comorbidity duration (without relying on multi-modal data or comprehensive medical records) and disease associations from biomedical knowledge graphs to deliver high-performance prediction. DAPNet is the first to apply multi-view graph contrastive learning to disease progression prediction tasks. Compared with other studies on comorbidities, DAPNet innovatively integrates molecular-level disease association information, combines disease co-occurrence and ICD10, and fully explores the associations between diseases; RESULTS: This study validated DAPNet using a de-identified clinical dataset derived from medical claims, which includes 2,714 patients and 10,856 visits. Meanwhile, a kidney dataset (606 patients) based on MIMIC-IV has also been constructed to fully validate its performance. The results showed that DAPNet achieved state-of-the-art performance on the severe pneumonia dataset (F1=0.84, with an improvement of 8.7%), and outperformed the six baseline models on the kidney disease dataset (F1=0.80, with an improvement of 21.3%). Through case analysis, we elucidated the clinical and molecular associations identified by the DAPNet model, which facilitated a better understanding and explanation of potential disease association, thereby providing interpretability for the model.

Conclusions: The proposed DAPNet, for the first time, utilizes comorbidity duration and disease associations network, enabling more accurate disease progression prediction based on a multi-view graph contrastive learning, which provides valuable insights for early diagnosis and treatment of patients. Based on disease association networks, our research has enhanced the interpretability of disease progression predictions.

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来源期刊
CiteScore
7.20
自引率
5.70%
发文量
297
审稿时长
1 months
期刊介绍: BMC Medical Informatics and Decision Making is an open access journal publishing original peer-reviewed research articles in relation to the design, development, implementation, use, and evaluation of health information technologies and decision-making for human health.
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