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Quantifying critical states of complex diseases using single-sample dynamic network biomarkers

Dynamic network biomarkers (DNB) can identify the critical state or tipping point of a disease, thereby predicting rather than diagnosing the disease. However, it is difficult to apply the DNB theory to clinical practice because evaluating DNB at the critical state required the data of multiple samp...

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Autores principales: Liu, Xiaoping, Chang, Xiao, Liu, Rui, Yu, Xiangtian, Chen, Luonan, Aihara, Kazuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5517040/
https://www.ncbi.nlm.nih.gov/pubmed/28678795
http://dx.doi.org/10.1371/journal.pcbi.1005633
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author Liu, Xiaoping
Chang, Xiao
Liu, Rui
Yu, Xiangtian
Chen, Luonan
Aihara, Kazuyuki
author_facet Liu, Xiaoping
Chang, Xiao
Liu, Rui
Yu, Xiangtian
Chen, Luonan
Aihara, Kazuyuki
author_sort Liu, Xiaoping
collection PubMed
description Dynamic network biomarkers (DNB) can identify the critical state or tipping point of a disease, thereby predicting rather than diagnosing the disease. However, it is difficult to apply the DNB theory to clinical practice because evaluating DNB at the critical state required the data of multiple samples on each individual, which are generally not available, and thus limit the applicability of DNB. In this study, we developed a novel method, i.e., single-sample DNB (sDNB), to detect early-warning signals or critical states of diseases in individual patients with only a single sample for each patient, thus opening a new way to predict diseases in a personalized way. In contrast to the information of differential expressions used in traditional biomarkers to “diagnose disease”, sDNB is based on the information of differential associations, thereby having the ability to “predict disease” or “diagnose near-future disease”. Applying this method to datasets for influenza virus infection and cancer metastasis led to accurate identification of the critical states or correct prediction of the immediate diseases based on individual samples. We successfully identified the critical states or tipping points just before the appearance of disease symptoms for influenza virus infection and the onset of distant metastasis for individual patients with cancer, thereby demonstrating the effectiveness and efficiency of our method for quantifying critical states at the single-sample level.
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spelling pubmed-55170402017-08-07 Quantifying critical states of complex diseases using single-sample dynamic network biomarkers Liu, Xiaoping Chang, Xiao Liu, Rui Yu, Xiangtian Chen, Luonan Aihara, Kazuyuki PLoS Comput Biol Research Article Dynamic network biomarkers (DNB) can identify the critical state or tipping point of a disease, thereby predicting rather than diagnosing the disease. However, it is difficult to apply the DNB theory to clinical practice because evaluating DNB at the critical state required the data of multiple samples on each individual, which are generally not available, and thus limit the applicability of DNB. In this study, we developed a novel method, i.e., single-sample DNB (sDNB), to detect early-warning signals or critical states of diseases in individual patients with only a single sample for each patient, thus opening a new way to predict diseases in a personalized way. In contrast to the information of differential expressions used in traditional biomarkers to “diagnose disease”, sDNB is based on the information of differential associations, thereby having the ability to “predict disease” or “diagnose near-future disease”. Applying this method to datasets for influenza virus infection and cancer metastasis led to accurate identification of the critical states or correct prediction of the immediate diseases based on individual samples. We successfully identified the critical states or tipping points just before the appearance of disease symptoms for influenza virus infection and the onset of distant metastasis for individual patients with cancer, thereby demonstrating the effectiveness and efficiency of our method for quantifying critical states at the single-sample level. Public Library of Science 2017-07-05 /pmc/articles/PMC5517040/ /pubmed/28678795 http://dx.doi.org/10.1371/journal.pcbi.1005633 Text en © 2017 Liu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Liu, Xiaoping
Chang, Xiao
Liu, Rui
Yu, Xiangtian
Chen, Luonan
Aihara, Kazuyuki
Quantifying critical states of complex diseases using single-sample dynamic network biomarkers
title Quantifying critical states of complex diseases using single-sample dynamic network biomarkers
title_full Quantifying critical states of complex diseases using single-sample dynamic network biomarkers
title_fullStr Quantifying critical states of complex diseases using single-sample dynamic network biomarkers
title_full_unstemmed Quantifying critical states of complex diseases using single-sample dynamic network biomarkers
title_short Quantifying critical states of complex diseases using single-sample dynamic network biomarkers
title_sort quantifying critical states of complex diseases using single-sample dynamic network biomarkers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5517040/
https://www.ncbi.nlm.nih.gov/pubmed/28678795
http://dx.doi.org/10.1371/journal.pcbi.1005633
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