Evidence map›Paper›PMID 42605381›Full record

ArticleJournal of inflammation research2026

Establishment of a Predictive Model for Mortality in Sepsis Patients Using WGCNA and Machine Learning Algorithms.

Yulong Bai, Yubiao Xu, Shihui Tan, Yisheng Huang, Xiaoxiang Huang, Zhaoyin Fu

Abstract read
In one paragraph

Article in Journal of inflammation research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yulong Bai *Department of Emergency, First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, People's Republic of China.
Yubiao Xu *Department of General Surgery, Guangxi Medical University Kaiyuan Langdong Hospital, Nanning, 530022, People's Republic of China.
Shihui TanDepartment of Emergency, First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, People's Republic of China.
Yisheng HuangDepartment of Critical Care Medicine, The First People's Hospital of Qinzhou, Qinzhou, 535009, People's Republic of China.
Xiaoxiang HuangDepartment of Critical Care Medicine, The First People's Hospital of Qinzhou, Qinzhou, 535009, People's Republic of China.
Zhaoyin FuDepartment of Critical Care Medicine, The First People's Hospital of Qinzhou, Qinzhou, 535009, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Predicting mortality in sepsis patients remains a challenge in clinical settings. This study aimed to identify genes associated with sepsis-related mortality and determine the predictive value of a model using these death-related genes. Methods: We employed Weighted Gene Co-expression Network Analysis (WGCNA), differential expression analysis, and machine learning (ML) algorithms to identify genes related to sepsis mortality by analyzing the GSE185263 dataset. A predictive model was constructed base on the genes related to sepsis mortality and validated using external cohorts. Blood samples from 120 sepsis patients were collected to test the expression of key genes. The predictive value of the key genes was verified in clinical samples. Results: WGCNA results revealed that the turquoise module was related to sepsis mortality. Thirty-five death-related genes were identified by intersecting module genes with differentially expressed genes between survivor and non-survivor samples. Three ML algorithms identified TMTC1, AMOTL1, and PTGFR as key genes. The model constructed with these three genes showed moderate predictive value. External cohorts with a total of 523 samples validated the predictive value of the model at moderate to high levels. Clinical sample results indicated that all three genes were elevated in deceased sepsis patients, and the predictive value was moderate. Combining the model with the APACHE II score achieved high predictive accuracy. Conclusion: This study identified and validated three genes related to sepsis mortality and established a predictive model that performed well in distinguishing sepsis patients at high risk of death.

Indexed as

genesmachine learning algorithmsmortalitypredictive modelsepsis

Identifiers

PMID42605381
PMCPMC13477669

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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.