Evidence map›Paper›PMID 36941583›Full record

ArticleMolecular medicine (Cambridge, Mass.)2023

Use of machine learning-based integration to develop a monocyte differentiation-related signature for improving prognosis in patients with sepsis.

Jingyuan Ning, Keran Sun, Xuan Wang, Xiaoqing Fan, Keqi Jia, Jinlei Cui, Cuiqing Ma

Open access · goldFull text read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Jingyuan Ning *Department of Immunology, Hebei Medical University, Shijiazhuang, People's Republic of China.
Keran Sun *Department of Immunology, Hebei Medical University, Shijiazhuang, People's Republic of China.
Xuan Wang *Department of Immunology, Hebei Medical University, Shijiazhuang, People's Republic of China.
Xiaoqing FanDepartment of Immunology, Hebei Medical University, Shijiazhuang, People's Republic of China.
Keqi JiaDepartment of Pathology, Shijiazhuang People's Hospital, Shijiazhuang, People's Republic of China.
Jinlei CuiDepartment of Immunology, Hebei Medical University, Shijiazhuang, People's Republic of China.
Cuiqing MaDepartment of Immunology, Hebei Medical University, Shijiazhuang, People's Republic of China. macuiqing@hebmu.edu.cn.ORCID 0000-0001-9021-7040
Hebei Medical University · CNFirst Hospital of Shijiazhuang · CN

Funding

Hebei Key R&D Program Project Special Project for the Construction of Beijing-Tianjin-Hebei Collaborative Innovation Community NO.22347702DHebei Province Graduate Innovation Funding Project XCXZZB202301Hebei Provincial Department of Education Grants for Cultivating Innovation Ability of Graduate Students at the Provincial Level CXZZBS2023107National Natural Science Foundation of China 81971474Natural Science Foundation of Hebei Province C2021206011
6 · The paper itself

Abstract

backgroundAlthough significant advances have been made in intensive care medicine and antibacterial treatment, sepsis is still a common disease with high mortality. The condition of sepsis patients changes rapidly, and each hour of delay in the administration of appropriate antibiotic treatment can lead to a 4-7% increase in fatality. Therefore, early diagnosis and intervention may help improve the prognosis of patients with sepsis.

methodsWe obtained single-cell sequencing data from 12 patients. This included 14,622 cells from four patients with bacterial infectious sepsis and eight patients with sepsis admitted to the ICU for other various reasons. Monocyte differentiation trajectories were analyzed using the "monocle" software, and differentiation-related genes were identified. Based on the expression of differentiation-related genes, 99 machine-learning combinations of prognostic signatures were obtained, and risk scores were calculated for all patients. The "scissor" software was used to associate high-risk and low-risk patients with individual cells. The "cellchat" software was used to demonstrate the regulatory relationships between high-risk and low-risk cells in a cellular communication network. The diagnostic value and prognostic predictive value of Enah/Vasp-like (EVL) were determined. Clinical validation of the results was performed with 40 samples. The "CBNplot" software based on Bayesian network inference was used to construct EVL regulatory networks.

resultsWe systematically analyzed three cell states during monocyte differentiation. The differential analysis identified 166 monocyte differentiation-related genes. Among the 99 machine-learning combinations of prognostic signatures constructed, the Lasso + CoxBoost signature with 17 genes showed the best prognostic prediction performance. The highest percentage of high-risk cells was found in state one. Cell communication analysis demonstrated regulatory networks between high-risk and low-risk cell subpopulations and other immune cells. We then determined the diagnostic and prognostic value of EVL stabilization in multiple external datasets. Experiments with clinical samples demonstrated the accuracy of this analysis. Finally, Bayesian network inference revealed potential network mechanisms of EVL regulation.

conclusionsMonocyte differentiation-related prognostic signatures based on the Lasso + CoxBoost combination were able to accurately predict the prognostic status of patients with sepsis. In addition, low EVL expression was associated with poor prognosis in sepsis.

Indexed as

MonocytesSepsisAnti-Bacterial AgentsBayes TheoremCell DifferentiationHumansMachine LearningAnti-Bacterial AgentsEVLMachine learningPrognosisSepsisSingle cell

Identifiers

PMID36941583
PMCPMC10029317
OpenAlexW4328049514

What OpenQuestion holds

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LicenceCC BY
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table measurements read14
Read underepoch 390

Registered trials

None linked

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.