Evidence map›Paper›PMID 36681676›Full record

ArticleCell death discovery2023

miR-150-5p in neutrophil-derived extracellular vesicles associated with sepsis-induced cardiomyopathy in septic patients.

Rongzong Ye, Qiuyun Lin, Wenkai Xiao, Lixia Mao, Pengfei Zhang, Lingshan Zhou, Xiaoxia Wu, Nannan Jiang, Xihe Zhang, Yinhua Zhang and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

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  11. An approach to evaluate the effect of inflammatory microvesicles on CaExperimental biology and medicine (Maywood, N.J.) · 2025
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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

14 authors at 3 institutions in 3 countries.

Rongzong Ye *Department of Critical Care Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524000, China.
Qiuyun Lin *Department of Critical Care Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524000, China.
Wenkai Xiao *Department of Critical Care Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524000, China.
Lixia MaoDepartment of Critical Care Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524000, China.
Pengfei ZhangDepartment of Critical Care Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524000, China.
Lingshan ZhouDepartment of Critical Care Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524000, China.
Xiaoxia WuDepartment of Critical Care Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524000, China.
Nannan JiangDepartment of Critical Care Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524000, China.
Xihe ZhangDoctoral Scientific Research Center, Lianjiang People's Hospital, Zhanjiang, 524400, China.
Yinhua ZhangDepartment of Physiology & Biomedical Sciences, Ischemic/hypoxic Disease Institute, Seoul National University College of Medicine, Seoul, 03080, Korea.
Daqing MaDivision of Anesthetics, Pain, Medicine and Intensive Care, Department of Surgery and Cancer, Faculty of Medicine, Imperial College, London, UK.ORCID http://orcid.org/0000-0002-0688-2097
Jiahao HuangDepartment of Critical Care Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524000, China. jhuangaf@connect.ust.hk.ORCID http://orcid.org/0000-0002-6190-456X
Xiaoyan WangDoctoral Scientific Research Center, Lianjiang People's Hospital, Zhanjiang, 524400, China. cc11wxy@126.com.ORCID http://orcid.org/0000-0002-8643-3215
Liehua DengDepartment of Critical Care Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524000, China. glinson@126.com.
Guangdong Medical College · CNChelsea and Westminster Hospital · GBSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionEarly diagnosis and potential therapeutic targets of sepsis-induced cardiomyopathy (SIC) remain challenges clinically. Circulating extracellular vesicles from immune cells carrying crucial injurious mediators, including miRNAs in sepsis. However, the impacts of neutrophil-derived extracellular vesicles and their miRNAs in the SIC development are unknown.

objectivesThe present study focused on the in-depth miRNA expression profiles of neutrophil-derived extracellular vesicles and explored the potential molecular biomarkers during the process of SIC.

methodsNeutrophil-derived extracellular vesicles were isolated from the blood samples in three sepsis patients with or without cardiomyopathy on day 1 and day 3 after ICU admission in comparison with three healthy controls. miRNAs were determined by RNA sequencing. The closely related differentially expressed miRNAs with SIC were further validated through qRT-PCR in the other cohorts of sepsis patients with (30 patients) or without cardiomyopathy (20 patients) and the association between miRNAs and the occurrence or disease severity of septic cardiomyopathy were stratified with logistic regression analysis.

resultsSixty-eight miRNAs from neutrophil-derived extracellular vesicles were changed significantly between healthy controls and without septic cardiomyopathy patients (61 miRNAs upregulated and seven downregulated). Thirty-eight miRNAs were differentially expressed in the septic cardiomyopathy patients. 27 common differentially expressed miRNAs were found in both groups with similar kinetics (23 miRNAs upregulated and four downregulated). The enriched cellular signaling pathway mediated by miRNAs from sepsis to septic cardiomyopathy was the HIF-1 signaling system modulated septic inflammation. Using multivariate logistic regression analysis, miR-150-5p coupled with NT-pro BNP, LVEF, and SOFA score (AUC = 0.941) were found to be the independent predictors of septic cardiomyopathy.

conclusionmiRNAs derived from neutrophil-derived extracellular vesicles play an important role in septic disease severity development towards cardiomyopathy. miR-150-5p may be a predictor of sepsis severity development but warrants further study.

Identifiers

PMID36681676
PMCPMC9867758
OpenAlexW4317662147

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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.