Evidence map›Paper›PMID 31938374›Full record

ArticleInternational journal of clinical and experimental pathology2018

Serum miR-126-3p level is down-regulated in sepsis patients.

Chao Chen, Lidan Zhang, Huimin Huang, Shanshan Liu, Yujian Liang, Lingling Xu, Suping Li, Yucai Cheng, Wen Tang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 29% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Review
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  4. MicroRNA-126 (MiR-126): key roles in related diseases.Journal of physiology and biochemistry · 2024
    Review
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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

9 authors at 1 institution in 1 country.

Chao ChenDepartment of Pediatric Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong, China.
Lidan ZhangDepartment of Pediatric Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong, China.
Huimin HuangDepartment of Pediatric Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong, China.
Shanshan LiuDepartment of Pediatric Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong, China.
Yujian LiangDepartment of Pediatric Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong, China.
Lingling XuDepartment of Pediatric Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong, China.
Suping LiDepartment of Pediatric Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong, China.
Yucai ChengDepartment of Pediatric Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong, China.
Wen TangDepartment of Pediatric Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, Guangdong, China.
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndothelial injury is part of the pathogenesis of sepsis. The microRNA-126 (miR-126) was previously identified as an endothelial biomarker and is known to play a critical role in preserving endothelial cell integrity. However, the role of miRNA-126 in sepsis is unclear.

methodBlood samples were collected from sepsis patients at the first Affiliated Hospital of Sun Yat-sen University within 24 h (n = 60) and on day 7 (n = 51) after diagnosis, and once from control subjects (n = 46). MiR-126-3p expression was evaluated by quantitative real-time PCR. The miR-126-3p level was correlated with clinical data and a set of routine and experimental biomarkers. The outcome of sepsis patients was determined by follow-up at 28 days after collection of blood samples on day 7.

resultMiR-126-3p level was significantly downregulated in sepsis patients 24 h after diagnosis compared with control subjects. Degree of downregulation of serum miR-126-3p correlated with the severity of sepsis. To determine the diagnostic accuracy of miR-126-3p, the receiver operating characteristic (ROC) was performed and the AUC of miR-126-3p was 0.735. Furthermore, serum miR-126-3p concentration at this time point was correlated with the expression markers of systemic inflammation, bacterial infection, and renal and hepatic dysfunction. However, serum miR-126-3p level on day 7 day did not differ between surviving sepsis patients and those who died.

conclusionThese results indicate that miR-126-3p could be a diagnostic biomarker for sepsis.

Indexed as

diagnosisendothelial injurymiR-126-3pprognosisSepsis

Identifiers

PMID31938374
PMCPMC6958305
OpenAlexW3020240891

What OpenQuestion holds

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Registered trials

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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.