Evidence map›Paper›PMID 36685531›Full record

ArticleFrontiers in immunology2022

Combination of transcriptional biomarkers and clinical parameters for early prediction of sepsis indued acute respiratory distress syndrome.

Ren-Qi Yao, Zong Shen, Qi-Min Ma, Ping Ling, Chen-Ru Wei, Li-Yu Zheng, Yu Duan, Wei Li, Feng Zhu, Yu Sun and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

11 authors at 3 institutions in 1 country.

Ren-Qi YaoDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Zong ShenDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Qi-Min MaDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Ping LingDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Chen-Ru WeiDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Li-Yu ZhengTranslational Medicine Research Center, Medical Innovation Research Division and Fourth Medical Center of the Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Yu DuanTranslational Medicine Research Center, Medical Innovation Research Division and Fourth Medical Center of the Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Wei LiDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Feng ZhuDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Yu SunDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Guo-Sheng WuDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai, China.
Second Military Medical University · CNChinese People's Liberation Army · CNChinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: As a common yet intractable complication of severe sepsis, acute respiratory distress syndrome (ARDS) is closely associated with poor clinical outcomes and elevated medical expenses. The aim of the current study is to generate a model combining transcriptional biomarkers and clinical parameters to alarm the development of ARDS in septic patients. Methods: Gene expression profile (GSE66890) was downloaded from the Gene Expression Omnibus database and clinical data were extracted. Differentially expressed genes (DEGs) from whole blood leukocytes were identified between patients with sepsis alone and septic patients who develop ARDS. ARDS prediction model was constructed using backward stepwise regression and Akaike Information Criterion (AIC). Meanwhile, a nomogram based on this model was established, with subsequent internal validation. Results: A total of 57 severe septic patients were enrolled in this study, and 28 (49.1%) developed ARDS. Based on the differential expression analysis, six DEGs (BPI, OLFM4, LCN2, CD24, MMP8 and MME) were screened. According to the outcome prediction model, six valuable risk factors (direct lung injury, shock, tumor, BPI, MME and MMP8) were incorporated into a nomogram, which was used to predict the onset of ARDS in septic patients. The calibration curves of the nomogram showed good consistency between the probabilities and observed values. The decision curve analysis also revealed the potential clinical usefulness of the nomogram. The area under the receiver operating characteristic (AUROC) for the prediction of ARDS occurrence in septic patients by the nomogram was 0.86 (95% CI = 0.767-0.952). A sensitivity analysis showed that the AUROC for the prediction of ARDS development in septic patients without direct lung injury was 0.967 (95% CI = 0.896-1.0). Conclusions: The nomogram based on transcriptional biomarkers and clinical parameters showed a good performance for the prediction of ARDS occurrence in septic patients.

Indexed as

Lung InjuryRespiratory Distress SyndromeSepsisBiomarkersEndrinHumansMatrix Metalloproteinase 8BiomarkersEndrinMatrix Metalloproteinase 8MMEacute respiratory distress syndromebiomarkergene expressionpredictionsepsis

Identifiers

PMID36685531
PMCPMC9846102
OpenAlexW4313481803

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.