Evidence map›Paper›PMID 31301104›Full record

ArticleJournal of clinical laboratory analysis2019

Potential role of circulating long noncoding RNA MALAT1 in predicting disease risk, severity, and patients' survival in sepsis.

Feng Geng, Wei Liu, Li Yu

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. mRedox biology · 2026
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  16. Long Noncoding RNA: Regulatory Mechanisms and Therapeutic Potential in Sepsis.Frontiers in cellular and infection microbiology · 2021
    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

3 authors at 1 institution in 1 country.

Feng GengDepartment of ICU, The Central Hospital Of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Wei LiuDepartment of ICU, The Central Hospital Of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Li YuDepartment of ICU, The Central Hospital Of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID https://orcid.org/0000-0002-1930-2987
Huazhong University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to investigate the plasma long noncoding RNA metastasis-associated lung adenocarcinoma transcript 1 (lncRNA MALAT1) expression with risk, severity, inflammation level, and prognosis in sepsis.

methodsOne hundred and ninety sepsis patients and 190 health controls (HCs) were consecutively recruited. Blood samples within 24 hours after admission of sepsis patients and those on enrollment of HCs were collected, and then, plasma was separated for lncRNA MALAT1 and miR-125b expressions detections by RT-qPCR. In sepsis patients, clinical data and 28-day mortality were recorded, and plasma inflammatory cytokines expressions were detected by ELISA.

resultsPlasma lncRNA MALAT1 expression was elevated in sepsis patients than HCs (P < 0.001), and ROC curve disclosed that it had a good value in predicting sepsis risk with an area under curve (AUC) of 0.823 (95% CI: 0.783-0.864). Additionally, lncRNA MALAT1 expression was positively correlated with Scr (P = 0.005), WBC (P = 0.017), CRP (P < 0.001), PCT (P < 0.001), TNF-α (P < 0.001), IL-8 (P < 0.001), IL-17 (P = 0.001), APACHE II score (P < 0.001), and SOFA score (P < 0.001). LncRNA MALA1 expression was elevated in deaths compared with survivors (P < 0.001) and could predict the risk of 28-day mortality with an AUC of 0.755 (95% CI: 0.682-0.828). Accumulating survival was worse in patients with lncRNA MALAT1 high expression compared with patients who had lncRNA MALAT1 low expression (P < 0.001). Moreover, lncRNA MALAT1 expression was negatively correlated with miR-125b level in both sepsis patients (P < 0.001) and HCs (P < 0.001).

conclusionLncRNA MALAT1 could be developed as a potential biomarker for facilitating diagnosis and management in sepsis patients.

Indexed as

Severity of Illness IndexAPACHEBiomarkersFemaleFollow-Up StudiesHumansInflammationMaleMiddle AgedPrognosisRisk FactorsRNA, Long NoncodingROC CurveSepsisSurvival RateBiomarkersMALAT1 long non-coding RNA, humanRNA, Long NoncodinglncRNA MALAT1miR-125bprognosisrisksepsisseverity

Identifiers

PMID31301104
PMCPMC6805255
OpenAlexW2958643898

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.