Evidence map›Paper›PMID 42023222›Full record

ArticleFrontiers in immunology2026

Identification of biomarkers for pediatric sepsis based on machine learning and bioinformatics analysis.

Weidong Ye, Sijia Chen, You Duan, Junwei Shan, Jian Wang, Heng Xu, Zhongyan Li, Cheng Guo

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Weidong Ye *Department of Pediatric, The Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, Zhejiang, China.
Sijia Chen *Department of Pediatric, The Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, Zhejiang, China.
You DuanWest China Institute of Women and Children's Health, West China Second University Hospital, Sichuan University, Chengdu, China.
Junwei ShanHuante Biotechnology Co. Ltd., Hangzhou, China.
Jian WangDepartment of Pediatric, The Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, Zhejiang, China.
Heng XuDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Zhongyan Li *Huante Biotechnology Co. Ltd., Hangzhou, China.
Cheng GuoDepartment of Pediatric, The Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pediatric sepsis is a systemic inflammatory syndrome caused by dysregulated host immune responses, with a high mortality rate and a lack of effective biomarkers, posing significant challenges for early diagnosis and treatment. This study integrated six bulk RNA-seq datasets related to pediatric sepsis, including 497 patients and 116 healthy control samples. Weighted gene co-expression network analysis was used to identify gene modules significantly associated with pediatric sepsis, and 237 high-confidence biomarkers were screened based on 14 machine learning models, among which RORA and GPR183 stood out in multiple models. Functional analysis indicated that these biomarkers were mainly involved in biological processes such as transcription and translation, the immune system, and cellular senescence. Immune infiltration analysis revealed a significant reduction in adaptive immune cells such as B cells and CD8

Indexed as

BiomarkersComputational BiologyMachine LearningSepsisAnimalsChildChild, PreschoolFemaleGene Expression ProfilingHumansMaleZebrafishBiomarkersbioinformatics analysisbiomarkersmachine learningpediatric sepsisRORA

Identifiers

PMID42023222
PMCPMC13095569

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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.