Evidence map›Paper›PMID 31764830›Full record

ArticleMedicine2019

The relationship of MicroRNA-21 and plaque stability in acute coronary syndrome.

Wangwei He, Liyuan Zhu, Yu Huang, Yinfen Zhang, Weimin Shen, Lihuan Fang, Jun Li, Zhuo Wang, Qiang Xie

Open access · goldAbstract read
In one paragraph

Article in Medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Vulnerable Atherosclerotic Plaque: Is There a Molecular Signature?International journal of molecular sciences · 2022
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. miR-21 in Human Cardiomyopathies.Frontiers in cardiovascular medicine · 2021
    Review
  15. Review
  16. Macrophage Plasticity and Atherosclerosis Therapy.Frontiers in molecular biosciences · 2021
    Review
  17. 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

9 authors at 1 institution in 1 country.

Wangwei HeDepartment of Cardiology, the First Affiliated Hospital of Xiamen University, Xiamen, Fujian Province.
Liyuan ZhuDepartment of Cardiology, the First Affiliated Hospital of Xiamen University, Xiamen, Fujian Province.
Yu HuangDepartment of Cardiology, the First Affiliated Hospital of Xiamen University, Xiamen, Fujian Province.
Yinfen ZhangDepartment of Cardiology, the First Affiliated Hospital of Xiamen University, Xiamen, Fujian Province.
Weimin ShenDepartment of Cardiology, the First Affiliated Hospital of Xiamen University, Xiamen, Fujian Province.
Lihuan FangDepartment of Cardiology, the First Affiliated Hospital of Xiamen University, Xiamen, Fujian Province.
Jun LiDepartment of Cardiology, the First Affiliated Hospital of Xiamen University, Xiamen, Fujian Province.
Zhuo WangDepartment of Cardiology, Renmin Hospital of Wuhan University, Cardiovascular Research Institute of Wuhan University, Wuhan, Hubei Province, China.
Qiang XieDepartment of Cardiology, the First Affiliated Hospital of Xiamen University, Xiamen, Fujian Province.
First Affiliated Hospital of Xiamen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute coronary syndrome (ACS) leads to clinical symptoms such as chest pain, dyspnea, and arrhythmia. The occurrence of ACS is mainly related to the vulnerable plaques in the coronary arteries. MicroRNA-21 (miR-21) is widely expressed in cardiovascular disease and considered as a marker of myocardial infarction, but its role in vulnerable atherosclerotic plaque of ACS is poorly studied. The cases of ACS and control group were selected in 2 years. Our results revealed that miR-21 was highly positively correlated with the maximum lipid core area, the number of diseased vessels, the number of macrophages, the number of vulnerable plaques, and negatively correlated with the thickness of fiber caps. In the high expression group, the number of coronary artery lesions, the number of vulnerable plaques, the core area of lipid pools and the number of macrophages were significantly higher than those in the low expression group and the middle expression group. But the high expression group of the thickness of the fiber cap was significantly lower than that of the low expression group and the medium expression group. These studies show that miR-21 is an important factor leading to vulnerable plaque instability in ACS, and it can be a predictor of acute adverse events in coronary heart disease.

Indexed as

Acute Coronary SyndromeFemaleHumansMaleMicroRNAsMiddle AgedPlaque, AtheroscleroticMicroRNAsMIRN21 microRNA, human

Identifiers

PMID31764830
PMCPMC6882643
OpenAlexW2990692644

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.