Evidence map›Paper›PMID 35562979›Full record

ReviewInternational journal of molecular sciences2022

Epigenetic Modifications and Non-Coding RNA in Diabetes-Mellitus-Induced Coronary Artery Disease: Pathophysiological Link and New Therapeutic Frontiers.

Francesca Romana Prandi, Dalgisio Lecis, Federica Illuminato, Marialucia Milite, Roberto Celotto, Stamatios Lerakis, Francesco Romeo, Francesco Barillà

Open access · goldAbstract readReview
In one paragraph

Review 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 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 29 citations in OpenAlex.

  1. Epigenetic regulation in a high-sugar environment (Review).International journal of molecular medicine · 2026
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  14. Metabolic memory: mechanisms and diseases.Signal transduction and targeted therapy · 2024
    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

8 authors at 3 institutions in 2 countries.

Francesca Romana PrandiDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.ORCID 0000-0003-1878-8871
Dalgisio LecisDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.
Federica IlluminatoDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.
Marialucia MiliteDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.
Roberto CelottoDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.ORCID 0000-0003-1837-5997
Stamatios LerakisDepartment of Cardiology, Mount Sinai Hospital, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Francesco RomeoDepartment of Departmental Faculty of Medicine, Unicamillus-Saint Camillus International University of Health and Medical Sciences, 00131 Rome, Italy.
Francesco BarillàDivision of Cardiology, Department of Systems Medicine, Tor Vergata University, 00133 Rome, Italy.ORCID 0000-0003-0594-7212
University of Rome Tor Vergata · ITMount Sinai Hospital · USSaint Camillus International University of Health and Medical Sciences · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetes mellitus (DM) is a glucose metabolism disorder characterized by chronic hyperglycemia resulting from a deficit of insulin production and/or action. DM affects more than 1 in 10 adults, and it is associated with an increased risk of cardiovascular morbidity and mortality. Cardiovascular disease (CVD) accounts for two thirds of the overall deaths in diabetic patients, with coronary artery disease (CAD) and ischemic cardiomyopathy as the main contributors. Hyperglycemic damage on vascular endothelial cells leading to endothelial dysfunction represents the main initiating factor in the pathogenesis of diabetic vascular complications; however, the underlying pathophysiological mechanisms are still not entirely understood. This review addresses the current knowledge on the pathophysiological links between DM and CAD with a focus on the role of epigenetic modifications, including DNA methylation, histone modifications and noncoding RNA control. Increased knowledge of epigenetic mechanisms has contributed to the development of new pharmacological treatments ("epidrugs") with epigenetic targets, although these approaches present several challenges. Specific epigenetic biomarkers may also be used to predict or detect the development and progression of diabetes complications. Further studies on diabetes and CAD epigenetics are needed in order to identify possible new therapeutic targets and advance personalized medicine with the prediction of individual drug responses and minimization of adverse effects.

Indexed as

Coronary Artery DiseaseDiabetes MellitusEndothelial CellsEpigenesis, GeneticHumansRNA, UntranslatedRNA, Untranslatedcoronary artery diseasediabetes mellitusepidrugsepigeneticshyperglycemia

Identifiers

PMID35562979
PMCPMC9105558
OpenAlexW4224212301

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.