Evidence map›Paper›PMID 29073904›Full record

ArticleJournal of translational medicine2017

Detecting the tipping points in a three-state model of complex diseases by temporal differential networks.

Pei Chen, Yongjun Li, Xiaoping Liu, Rui Liu, Luonan Chen

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Article in Journal of translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

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31citing papers in PubMed
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3 · Its place in the literature

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31 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Pei ChenSchool of Computer Science and Engineering, South China University of Technology, Guangzhou, 510640, China.
Yongjun LiSchool of Computer Science and Engineering, South China University of Technology, Guangzhou, 510640, China.
Xiaoping LiuSchool of Mathematics and Statistics, Shandong University at Weihai, Weihai, 264209, China.
Rui LiuSchool of Mathematics, South China University of Technology, Guangzhou, 510640, China. scliurui@scut.edu.cn.
Luonan ChenCollaborative Research Center for Innovative Mathematical Modelling, University of Tokyo, Tokyo, 153-8505, Japan. lnchen@sibs.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe progression of complex diseases, such as diabetes and cancer, is generally a nonlinear process with three stages, i.e., normal state, pre-disease state, and disease state, where the pre-disease state is a critical state or tipping point immediately preceding the disease state. Traditional biomarkers aim to identify a disease state by exploiting the information of differential expressions for the observed molecules, but may fail to detect a pre-disease state because there are generally little significant differences between the normal and pre-disease states. Thus, it is challenging to signal the pre-disease state, which actually implies the disease prediction.

methodsIn this work, by exploiting the information of differential associations among the observed molecules between the normal and pre-disease states, we propose a temporal differential network based computational method to accurately signal the pre-disease state or predict the occurrence of severe disease. The theoretical foundation of this work is the quantification of the critical state using dynamical network biomarkers.

resultsConsidering that there is one stationary Markov process before reaching the tipping point, a novel index, inconsistency score (I-score), is proposed to quantitatively measure the change of the stationary processes from the normal state so as to detect the onset of pre-disease state. In other words, a drastic increase of I-score implies the high inconsistency with the preceding stable state and thus signals the upcoming critical transition. This approach is applied to the simulated and real datasets of three diseases, which demonstrates the effectiveness of our method for predicting the deterioration into disease states. Both functional analysis and pathway enrichment also validate the computational results from the perspectives of both molecules and networks.

conclusionsAt the molecular network level, this method provides a computational way of unravelling the underlying mechanism of the dynamical progression when a biological system is near the tipping point, and thus detecting the early-warning signal of the imminent critical transition, which may help to achieve timely intervention. Moreover, the rewiring of differential networks effectively extracts discriminatively interpretable features, and systematically demonstrates the dynamical change of a biological system.

Indexed as

Disease ProgressionGene Regulatory NetworksDatabases, GeneticHumansMarkov ChainsNumerical Analysis, Computer-AssistedOligonucleotide Array Sequence AnalysisReproducibility of ResultsTime FactorsCritical transitionDifferential networkDynamical network biomarkerHidden Markov modelPre-disease stateTipping point

Identifiers

PMID29073904
PMCPMC5658963

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.