Department of Bioinformatics, Fraunhofer Institute for Algorithms and Scientific Computing (SCAI), Sankt Augustin, Germany.
Bonn-Aachen International Center for Information Technology (B-IT), University of Bonn, Bonn, Germany.
PLoS Comput Biol. 2023 Feb 13;19(2):e1009894. doi: 10.1371/journal.pcbi.1009894. eCollection 2023 Feb.
Modeling biological mechanisms is a key for disease understanding and drug-target identification. However, formulating quantitative models in the field of Alzheimer's Disease is challenged by a lack of detailed knowledge of relevant biochemical processes. Additionally, fitting differential equation systems usually requires time resolved data and the possibility to perform intervention experiments, which is difficult in neurological disorders. This work addresses these challenges by employing the recently published Variational Autoencoder Modular Bayesian Networks (VAMBN) method, which we here trained on combined clinical and patient level gene expression data while incorporating a disease focused knowledge graph. Our approach, called iVAMBN, resulted in a quantitative model that allowed us to simulate a down-expression of the putative drug target CD33, including potential impact on cognitive impairment and brain pathophysiology. Experimental validation demonstrated a high overlap of molecular mechanism predicted to be altered by CD33 perturbation with cell line data. Altogether, our modeling approach may help to select promising drug targets.
建立生物机制模型是理解疾病和确定药物靶点的关键。然而,由于缺乏对相关生化过程的详细了解,阿尔茨海默病领域的定量建模面临挑战。此外,微分方程系统的拟合通常需要时间分辨数据和进行干预实验的可能性,而这在神经疾病中是困难的。这项工作通过使用最近发表的变分自动编码器模块化贝叶斯网络(VAMBN)方法来应对这些挑战,我们在这项研究中,对联合临床和患者水平的基因表达数据进行了训练,同时纳入了一个专注于疾病的知识图谱。我们的方法称为 iVAMBN,得到了一个定量模型,使我们能够模拟假定药物靶点 CD33 的下调表达,包括对认知障碍和大脑病理生理学的潜在影响。实验验证表明,通过 CD33 干扰预测的分子机制与细胞系数据有很高的重叠。总之,我们的建模方法可能有助于选择有前途的药物靶点。