Evidence map›Paper›PMID 34914790›Full record

ArticlePloS one2021

Circulating miR-147b as a diagnostic marker for patients with bacterial sepsis and septic shock.

Ngo Tat Trung, Tran Thi Lien, Vu Viet Sang, Nghiem Xuan Hoan, Nguyen Dang Manh, Nguyen Sy Thau, Dao Thanh Quyen, Tran Thi Thu Hien, Phan Quoc Hoan, Mai Hong Bang and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
0.5field-weighted citation impact, top 42% 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. MicroRNAs in sepsis: Advances in diagnosis and prognostic monitoring.World journal of critical care medicine · 2026
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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

12 authors at 4 institutions in 2 countries.

Ngo Tat TrungCentre for Genetics Consultation and Cancer Screening, Hanoi, Vietnam.ORCID 0000-0001-9808-1176
Tran Thi LienVietnamese-German Center for Medical Research, Hanoi, Vietnam.
Vu Viet SangVietnamese-German Center for Medical Research, Hanoi, Vietnam.
Nghiem Xuan HoanVietnamese-German Center for Medical Research, Hanoi, Vietnam.
Nguyen Dang ManhVietnamese-German Center for Medical Research, Hanoi, Vietnam.
Nguyen Sy ThauVietnamese-German Center for Medical Research, Hanoi, Vietnam.
Dao Thanh QuyenVietnamese-German Center for Medical Research, Hanoi, Vietnam.
Tran Thi Thu HienDepartment of Molecular Biology, Hanoi, Vietnam.
Phan Quoc HoanDepartment of Molecular Biology, Hanoi, Vietnam.
Mai Hong BangVietnamese-German Center for Medical Research, Hanoi, Vietnam.
Thirumalaisamy P VelavanVietnamese-German Center for Medical Research, Hanoi, Vietnam.
Le Huu SongVietnamese-German Center for Medical Research, Hanoi, Vietnam.
Hanoi Medical University · VNVietnamese - German Center of Excellence in Medical Research · VNCenter for Health Consultation and Community Development · VNUniversitätsklinikum Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarly diagnosis, precise antimicrobial treatment and subsequent patient stratification can improve sepsis outcomes. Circulating biomarkers such as plasma microRNAs (miRNAs) have proven to be surrogates for diagnosis, severity and case management of infections. The expression of four selected miRNAs (miR-146-3p, miR-147b, miR-155 and miR-223) was validated for their prognostic and diagnostic potential in a clinically defined cohort of patients with sepsis and septic shock.

methodsThe expression of plasma miRNAs was quantified by quantitative PCR (qPCR) in patients with bacterial sepsis (n = 78), in patients with septic shock (n = 52) and in patients with dengue haemorrhagic fever (DHF; n = 69) and in healthy controls (n = 82).

resultsThe expression of studied miRNA was significantly increased in patients with bacterial sepsis and septic shock. The plasma miR-147b was able to differentiate bacterial sepsis from non-sepsis and septic shock (AUC = 0.77 and 0.8, respectively, p≤ 0.05), while the combination of plasma miR-147b and procalcitonin (PCT) predicted septic shock (AUC = 0.86, p≤ 0.05).

conclusionsThe plasma miR-147b may be an useful biomarker independently or in combination with PCT to support clinical diagnosis of sepsis and equally prognosis of patients with septic shock.

Indexed as

AdultAgedAged, 80 and overBiomarkersCalcitoninCirculating MicroRNACohort StudiesEarly DiagnosisFemaleGene ExpressionHumansMaleMicroRNAsMiddle AgedProcalcitoninPrognosisBiomarkersCalcitoninCirculating MicroRNAMicroRNAsMIR223, humanMIRN146 microRNA, humanMIRN147 microRNA, humanMIRN155 microRNA, humanProcalcitonin

Identifiers

PMID34914790
PMCPMC8675720
OpenAlexW4200465598

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.