Evidence map›Paper›PMID 36855207›Full record

ArticleEuropean journal of medical research2023

Identification and verification of feature biomarkers associated with immune cells in neonatal sepsis.

Weiqiang Liao, Huimin Xiao, Jinning He, Lili Huang, Yanxia Liao, Jiaohong Qin, Qiuping Yang, Liuhong Qu, Fei Ma, Sitao Li

Open access · goldAbstract read
In one paragraph

Article in European journal of medical research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. A practical predictive model to predict 30-day mortality in neonatal sepsis.Revista da Associacao Medica Brasileira (1992) · 2024
    Article
  11. Article
  12. Article
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

10 authors at 4 institutions in 1 country.

Weiqiang Liao *Department of Pediatrics, Dongguan Houjie Hospital, Dongguan, 523945, China.
Huimin Xiao *Department of Pediatrics, Dongguan Houjie Hospital, Dongguan, 523945, China.
Jinning HeDepartment of Pediatrics, Dongguan Houjie Hospital, Dongguan, 523945, China.
Lili HuangDepartment of Pediatrics, Dongguan Houjie Hospital, Dongguan, 523945, China.
Yanxia LiaoDepartment of Pediatrics, Dongguan Houjie Hospital, Dongguan, 523945, China.
Jiaohong QinDepartment of Pediatrics, Dongguan Houjie Hospital, Dongguan, 523945, China.
Qiuping YangDepartment of Pediatrics, The Sixth Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510655, China.
Liuhong QuDepartment of Neonatology, The Maternal and Child Health Care Hospital of Huadu, Guangzhou, 510800, China. quliuhong@163.com.
Fei MaDepartment of Neonatology, Maternal and Child Health Research Institute, Zhuhai Women and Children's Hospital, Zhuhai, 519001, China. mafei7@mail.sysu.edu.cn.
Sitao LiDepartment of Pediatrics, The Sixth Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510655, China. lisit@mail.sysu.edu.cn.
Dongguan People’s Hospital · CNSixth Affiliated Hospital of Sun Yat-sen University · CNInner Mongolia Maternal and Child Health · CNWeihai Maternal and Child Health Hospital · CN

Funding

Dongguan Social Science and Technology Development 201950715023152the Science and Technology Foundation of Guangzhou 202002030008the Science and Technology Foundation of Guangzhou 202103000071
6 · The paper itself

Abstract

backgroundNeonatal sepsis (NS), a life-threatening condition, is characterized by organ dysfunction and is the most common cause of neonatal death. However, the pathogenesis of NS is unclear and the clinical inflammatory markers currently used are not ideal for diagnosis of NS. Thus, exploring the link between immune responses in NS pathogenesis, elucidating the molecular mechanisms involved, and identifying potential therapeutic targets is of great significance in clinical practice. Herein, our study aimed to explore immune-related genes in NS and identify potential diagnostic biomarkers. Datasets for patients with NS and healthy controls were downloaded from the GEO database; GSE69686 and GSE25504 were used as the analysis and validation datasets, respectively. Differentially expressed genes (DEGs) were identified and Gene Set Enrichment Analysis (GSEA) was performed to determine their biological functions. Composition of immune cells was determined and immune-related genes (IRGs) between the two clusters were identified and their metabolic pathways were determined. Key genes with correlation coefficient > 0.5 and p < 0.05 were selected as screening biomarkers. Logistic regression models were constructed based on the selected biomarkers, and the diagnostic models were validated.

resultsFifty-two DEGs were identified, and GSEA indicated involvement in acute inflammatory response, bacterial detection, and regulation of macrophage activation. Most infiltrating immune cells, including activated CD8 + T cells, were significantly different in patients with NS compared to the healthy controls. Fifty-four IRGs were identified, and GSEA indicated involvement in immune response and macrophage activation and regulation of T cell activation. Diagnostic models of DEGs containing five genes (PROS1, TDRD9, RETN, LOC728401, and METTL7B) and IRG with one gene (NSUN7) constructed using LASSO algorithm were validated using the GPL6947 and GPL13667 subset datasets, respectively. The IRG model outperformed the DEG model. Additionally, statistical analysis suggested that risk scores may be related to gestational age and birth weight, regardless of sex.

conclusionsWe identified six IRGs as potential diagnostic biomarkers for NS and developed diagnostic models for NS. Our findings provide a new perspective for future research on NS pathogenesis.

Indexed as

Neonatal SepsisAlgorithmsBiomarkersHumansInfant, NewbornInflammationLogistic ModelsBiomarkersBiomarkersDiagnosis modelImmune infiltrationLogistic regressionNeonatal sepsis

Identifiers

PMID36855207
PMCPMC9972688
OpenAlexW4322719322

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.