Evidence map›Paper›PMID 36555301›Full record

ArticleInternational journal of molecular sciences2022

Deciphering the Role of miR-200c-3p in Type 1 Diabetes (Subclinical Cardiovascular Disease) and Its Correlation with Inflammation and Vascular Health.

Sherin Bakhashab, Megan Li Yuen Yeoh, David J Coulson, Samuel Christian Steel, Sabina L Ray, Jolanta U Weaver

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Endothelial Dysfunction in Diabetes Mellitus: New Insights.International journal of molecular sciences · 2023
    Review
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

6 authors at 3 institutions in 2 countries.

Sherin BakhashabBiochemistry Department, King Abdulaziz University, Jeddah 21589, Saudi Arabia.ORCID 0000-0003-1580-0409
Megan Li Yuen YeohTranslational & Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.ORCID 0000-0003-4579-8282
David J CoulsonTranslational & Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Samuel Christian SteelTranslational & Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Sabina L RayTranslational & Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Jolanta U WeaverTranslational & Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Newcastle University · GBKing Abdulaziz University · SAQueen Elizabeth Hospital · GB

Funding

Diabetes Research and Wellness Foundation open funding 2011Diabetes Research Fund, Queen Elizabeth Hospital, Gateshead, UK None
6 · The paper itself

Abstract

Uncomplicated type 1 diabetes (T1DM) displays all features of subclinical cardiovascular disease (CVD) as is associated with inflammation, endothelial dysfunction and low endothelial progenitor cells. MiR-200c-3p has been shown in animal tissues to be pro-atherogenic. We aimed to explore the role of miR-200c-3p in T1DM, a model of subclinical CVD. 19 samples from T1DM patients and 20 from matched controls (HC) were analyzed. MiR-200c in plasma and peripheral blood mononuclear cells (PBMCs) was measured by real-time quantitative polymerase chain reaction. The results were compared with the following indices of vascular health: circulating endothelial progenitor cells, (CD45dimCD34+VEGFR-2+ or CD45dimCD34+CD133+) and proangiogenic cells (PACs). MiR-200c-3p was significantly downregulated in PBMCs but not in plasma in T1DM. There was a significant negative correlation between the expression of miR-200c-3p and HbA1c, interleukin-7 (IL-7), vascular endothelial growth factor-C (VEGF-C), and soluble vascular cell adhesion molecule-1, and a positive correlation with CD45dimCD34+VEGFR-2+, CD45dimCD34+CD133+ and PACs. Receiver operating curve analyses showed miR-200c-3p as a biomarker for T1DM with significant downregulation of miR-200c-3p, possibly defining subclinical CVD at HbA1c > 44.8 mmol/mol (6.2%). In conclusion, downregulated miR-200c-3p in T1DM correlated with diabetic control, VEGF signaling, inflammation, vascular health and targeting VEGF signaling, and may define subclinical CVD. Further prospective studies are necessary to validate our findings in a larger group of patients.

Indexed as

Cardiovascular DiseasesDiabetes Mellitus, Type 1MicroRNAsAnimalsAntigens, CD34Glycated HemoglobinInflammationLeukocytes, MononuclearProspective StudiesVascular Endothelial Growth Factor AVascular Endothelial Growth Factor CVascular Endothelial Growth Factor Receptor-2Antigens, CD34Glycated HemoglobinMicroRNAsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor CVascular Endothelial Growth Factor Receptor-2cardiovascular diseasecirculating endothelial progenitor cellsinflammationmiR-200c-3pproangiogenic cellstype 1 diabetes mellitus

Identifiers

PMID36555301
PMCPMC9778946
OpenAlexW4312123528

What OpenQuestion holds

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LicenceCC BY
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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.