Evidence map›Paper›PMID 38512768›Full record

ArticleGut microbes

mNFE: microbiome network flow entropy for detecting pre-disease states of type 1 diabetes.

Rong Gao, Peiluan Li, Yueqiong Ni, Xueqing Peng, Jing Ren, Luonan Chen

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Article in Gut microbes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

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6 authors.

Rong GaoSchool of Mathematics and Statistics, Henan University of Science and Technology, Luoyang, China.
Peiluan LiSchool of Mathematics and Statistics, Henan University of Science and Technology, Luoyang, China.ORCID 0000-0001-5545-6185
Yueqiong NiDepartment of Microbiome Dynamics, Leibniz Institute for Natural Product Research and Infection Biology, Hans Knöll Institute, Jena, Germany.
Xueqing PengSchool of Mathematics and Statistics, Henan University of Science and Technology, Luoyang, China.
Jing RenSchool of Mathematics and Statistics, Henan University of Science and Technology, Luoyang, China.
Luonan ChenKey Laboratory of Systems Biology, Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, Shanghai, China.ORCID 0000-0002-3960-0068

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the development of Type 1 diabetes (T1D), there are critical states just before drastic changes, and identifying these pre-disease states may predict T1D or provide crucial early-warning signals. Unlike gene expression data, gut microbiome data can be collected noninvasively from stool samples. Gut microbiome sequencing data contain different levels of phylogenetic information that can be utilized to detect the tipping point or critical state in a reliable manner, thereby providing accurate and effective early-warning signals. However, it is still difficult to detect the critical state of T1D based on gut microbiome data due to generally non-significant differences between healthy and critical states. To address this problem, we proposed a new method - microbiome network flow entropy (mNFE) based on a single sample from each individual - for detecting the critical state before seroconversion and abrupt transitions of T1D at various taxonomic levels. The numerical simulation validated the robustness of mNFE under different noise levels. Furthermore, based on real datasets, mNFE successfully identified the critical states and their dynamic network biomarkers (DNBs) at different taxonomic levels. In addition, we found some high-frequency species, which are closely related to the unique clinical characteristics of autoantibodies at the four levels, and identified some non-differential 'dark species' play important roles during the T1D progression. mNFE can robustly and effectively detect the pre-disease states at various taxonomic levels and identify the corresponding DNBs with only a single sample for each individual. Therefore, our mNFE method provides a new approach not only for T1D pre-disease diagnosis or preventative treatment but also for preventative medicine of other diseases by gut microbiome.

Indexed as

Diabetes Mellitus, Type 1Gastrointestinal MicrobiomeBiomarkersDinitrofluorobenzeneEntropyHumansPhylogeny2,4-dinitrofluorobenzene sulfonic acidBiomarkersDinitrofluorobenzenedynamic network biomarker (DNB)gut microbiomenetwork flow entropy (NFE)Tipping pointType 1 diabetes (T1D)

Identifiers

PMID38512768
PMCPMC10962612

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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.