4.6 Article

PINNet: a deep neural network with pathway prior knowledge for Alzheimer's disease

Journal

FRONTIERS IN AGING NEUROSCIENCE
Volume 15, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fnagi.2023.1126156

Keywords

Alzheimer's disease; machine learning; transcriptomics; biomarkers; bioinformatics; protein-protein interaction network; interpretable machine learning

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Researchers propose a pathway information-based neural network (PINNet) to predict Alzheimer's Disease (AD) patients and analyze blood and brain transcriptomic signatures using an interpretable deep learning model. PINNet incorporates pathway prior knowledge from databases and reveals essential pathways and genes for predicting AD. Experimental results demonstrate that PINNet performs well in predicting AD using blood and brain gene expressions, outperforming or being similar to deep learning models without pathway information. Pathway analysis reveals enriched pathways related to cell migration, PI3K-Akt signaling, MAPK signaling, apoptosis, protein ubiquitination, and T-cell activation.
Introduction: Identification of Alzheimer's Disease (AD)-related transcriptomic signatures fromblood is important for early diagnosis of the disease. Deep learning techniques are potent classifiers for AD diagnosis, but most have been unable to identify biomarkers because of their lack of interpretability. Methods: To address these challenges, we propose a pathway information-based neural network (PINNet) to predict AD patients and analyze blood and brain transcriptomic signatures using an interpretable deep learning model. PINNet is a deep neural network (DNN) model with pathway prior knowledge from either the Gene Ontology or Kyoto Encyclopedia of Genes and Genomes databases. Then, a backpropagation-based model interpretation method was applied to reveal essential pathways and genes for predicting AD. Results: The performance of PINNet was compared with a DNN model without a pathway. Performances of PINNet outperformed or were similar to those of DNN without a pathway using blood and brain gene expressions, respectively. Moreover, PINNet considers more AD-related genes as essential features than DNN without a pathway in the learning process. Pathway analysis of protein-protein interaction modules of highly contributed genes showed that AD-related genes in blood were enriched with cell migration, PI3K-Akt, MAPK signaling, and apoptosis in blood. The pathways enriched in the brain module included cell migration, PI3K-Akt, MAPK signaling, apoptosis, protein ubiquitination, and t-cell activation. Discussion: By integrating prior knowledge about pathways, PINNet can reveal essential pathways related to AD. The source codes are available at https://github. com/DMCB-GIST/PINNet.

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