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

MOTIVATION: 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 t...

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Autores principales: Yan, Jinling, Li, Peiluan, Gao, Rong, Li, Ying, Chen, Luonan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8212786/
https://www.ncbi.nlm.nih.gov/pubmed/34150649
http://dx.doi.org/10.3389/fonc.2021.684781
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author Yan, Jinling
Li, Peiluan
Gao, Rong
Li, Ying
Chen, Luonan
author_facet Yan, Jinling
Li, Peiluan
Gao, Rong
Li, Ying
Chen, Luonan
author_sort Yan, Jinling
collection PubMed
description MOTIVATION: 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.
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spelling pubmed-82127862021-06-19 Identifying Critical States of Complex Diseases by Single-Sample Jensen-Shannon Divergence Yan, Jinling Li, Peiluan Gao, Rong Li, Ying Chen, Luonan Front Oncol Oncology MOTIVATION: 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. Frontiers Media S.A. 2021-06-04 /pmc/articles/PMC8212786/ /pubmed/34150649 http://dx.doi.org/10.3389/fonc.2021.684781 Text en Copyright © 2021 Yan, Li, Gao, Li and Chen https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Yan, Jinling
Li, Peiluan
Gao, Rong
Li, Ying
Chen, Luonan
Identifying Critical States of Complex Diseases by Single-Sample Jensen-Shannon Divergence
title Identifying Critical States of Complex Diseases by Single-Sample Jensen-Shannon Divergence
title_full Identifying Critical States of Complex Diseases by Single-Sample Jensen-Shannon Divergence
title_fullStr Identifying Critical States of Complex Diseases by Single-Sample Jensen-Shannon Divergence
title_full_unstemmed Identifying Critical States of Complex Diseases by Single-Sample Jensen-Shannon Divergence
title_short Identifying Critical States of Complex Diseases by Single-Sample Jensen-Shannon Divergence
title_sort identifying critical states of complex diseases by single-sample jensen-shannon divergence
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8212786/
https://www.ncbi.nlm.nih.gov/pubmed/34150649
http://dx.doi.org/10.3389/fonc.2021.684781
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