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Identifying Critical States of Complex Diseases by Single-Sample Jensen-Shannon Divergence.

AbstractMOTIVATION:
The evolution of complex diseases can be modeled as a time-dependent nonlinear dynamic system, and its progression can be divided into three states, i.e., the normal state, the pre-disease state and the disease state. The sudden deterioration of the disease can be regarded as the state transition of the dynamic system at the critical state or pre-disease state. How to detect the critical state of an individual before the disease state based on single-sample data has attracted many researchers' attention.
METHODS:
In this study, we proposed a novel approach, i.e., single-sample-based Jensen-Shannon Divergence (sJSD) method to detect the early-warning signals of complex diseases before critical transitions based on individual single-sample data. The method aims to construct score index based on sJSD, namely, inconsistency index (ICI).
RESULTS:
This method is applied to five real datasets, including prostate cancer, bladder urothelial carcinoma, influenza virus infection, cervical squamous cell carcinoma and endocervical adenocarcinoma and pancreatic adenocarcinoma. The critical states of 5 datasets with their corresponding sJSD signal biomarkers are successfully identified to diagnose and predict each individual sample, and some "dark genes" that without differential expressions but are sensitive to ICI score were revealed. This method is a data-driven and model-free method, which can be applied to not only disease prediction on individuals but also targeted drug design of each disease. At the same time, the identification of sJSD signal biomarkers is also of great significance for studying the molecular mechanism of disease progression from a dynamic perspective.
AuthorsJinling Yan, Peiluan Li, Rong Gao, Ying Li, Luonan Chen
JournalFrontiers in oncology (Front Oncol) Vol. 11 Pg. 684781 ( 2021) ISSN: 2234-943X [Print] Switzerland
PMID34150649 (Publication Type: Journal Article)
CopyrightCopyright © 2021 Yan, Li, Gao, Li and Chen.

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