Evidence map›Paper›PMID 41602763›Full record

ArticleFrontiers in microbiology2025

Dysbiosis and metabolic pathway shifts in the gut microbiome of children with sepsis: a comparative analysis.

Jiayue Xu, Jiru Li, Xiangmei Kong, Chen Zhang, Baocui Qi, Xiaodong Zhu, Yueniu Zhu, Yaya Xu

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Review
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.

Jiayue Xu *Department of Pediatric Critical Care Medicine, Xinhua Hospital Affiliated with the Medical School of Shanghai Jiao Tong University, Shanghai, China.
Jiru Li *Department of Pediatric Critical Care Medicine, Xinhua Hospital Affiliated with the Medical School of Shanghai Jiao Tong University, Shanghai, China.
Xiangmei KongDepartment of Pediatric Critical Care Medicine, Xinhua Hospital Affiliated with the Medical School of Shanghai Jiao Tong University, Shanghai, China.
Chen ZhangDepartment of Medicine, Dinfectome Inc., Nanjing, China.
Baocui QiBioinformatics and System Development Department, Dinfectome Inc., Nanjing, China.
Xiaodong ZhuDepartment of Pediatric Critical Care Medicine, Xinhua Hospital Affiliated with the Medical School of Shanghai Jiao Tong University, Shanghai, China.
Yueniu ZhuDepartment of Pediatric Critical Care Medicine, Xinhua Hospital Affiliated with the Medical School of Shanghai Jiao Tong University, Shanghai, China.
Yaya XuDepartment of Pediatric Critical Care Medicine, Xinhua Hospital Affiliated with the Medical School of Shanghai Jiao Tong University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The newly published Phoenix Sepsis Score in 2024 for assessing sepsis in children mainly focuses on respiratory, cardiological, coagulation and neurological indicators, whereas the gut microbiome also plays key roles in the occurrence and progression of sepsis. Additionally, emerging evidence suggests that specific biomarkers in gut microbiome are associated with disease progression. This study aimed to explore the differences in gut microbiome diversity, composition and function between septic and healthy children, and to establish correlations with clinical indicators and outcomes, providing new possibilities for the diagnosis and treatment of sepsis. Results: Analysis of gut microbiome was performed in 20 sepsis children and 9 healthy controls aged between 3 and 18 years old. The anal swab samples were analyzed by metagenomic next-generation sequencing. Significant differences were observed in Conclusion: Significant differences in diversity, taxa composition and gene function in the gut microbiome existed between septic and healthy children. The associations between gut microbiome dysbiosis and clinical indicators were identified.

Indexed as

gut microbiome dysbiosisKEGG pathwaymetagenomic next-generation sequencepediatricSepsis

Identifiers

PMID41602763
PMCPMC12834510

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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.