Evidence map›Paper›PMID 29704210›Full record

ReviewJournal of nephrology2018

Epicardial adipose tissue: new parameter for cardiovascular risk assessment in high risk populations.

Roberta Russo, Biagio Di Iorio, Luca Di Lullo, Domenico Russo

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Journal of nephrology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06557811 (Effect of Oral Semaglutide on Epicardial and Pericoronary Adipose Tissues in Type 2 Diabetes After Myocardial Infarction), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-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.

NCT06557811 phase4not yet recruitingstarted 2024, after this paper: background citation

Effect of Oral Semaglutide on Epicardial and Pericoronary Adipose Tissues in Type 2 Diabetes After Myocardial Infarction: a Randomized and Double-blind Clinical Trial

Ran2024Enrolled88Registered outcomes26Posted comparisons0ConditionsAcute Myocardial Infarction, Diabetic PatientsArmssemaglutide
Open the trial in the graph
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Right atrial wall inflammation detected byBMC cardiovascular disorders · 2023
    Article
  4. Article
  5. Article
  6. Epicardial Adipose Tissue in Patients with Coronary Artery Disease: A Meta-Analysis.Journal of cardiovascular development and disease · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Epicardial Adipose Tissue and Renal Disease.Journal of clinical medicine · 2019
    Review
  15. 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

4 authors at 3 institutions in 1 country.

Roberta RussoNephrology Unit, Department of Public Health, University FEDERICO II, Naples, Italy.
Biagio Di IorioNephrology Unit, "A. Landolfi" Hospital, Solofra, Avellino, Italy.
Luca Di LulloDepartment of Nephrology and Dialysis, "L. Parodi Delfino" Hospital, Colleferro, Rome, Italy.
Domenico RussoNephrology Unit, Department of Public Health, University FEDERICO II, Naples, Italy. domenicorusso51@hotmail.com.ORCID http://orcid.org/0000-0003-1285-8517
Federico II University Hospital · ITCTO Hospital · ITOspedale Antonio Cardarelli · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epicardial adipose tissue (EAT) is localized between the myocardial surface and visceral layer of the pericardium. It is a metabolically active organ that secretes several cytokines which modulate cardiovascular morphology and function. EAT may interact locally with coronary arteries through paracrine secretion mechanisms. Cytokines from peri-adventitial EAT may pass through the coronary wall by diffusion from the outside to the inside, interacting with cells. An additional potential mechanism by which EAT interacts locally with coronary arteries may be the vasocrine secretion.EAT may play a significant role as a modulator of cardiac functions. In physiologic conditions, EAT has biochemical cardio-protective properties, secreting anti-atherosclerosis substances; in metabolic disease states, EAT secretes bioactive molecules that may play an important role in the pathogenesis of coronary artery disease and cardiac arrhythmias by promoting atherosclerosis. EAT has been evaluated both in the general population and in metabolic disease states that are characterized by inflammation, such as cardiovascular diseases and chronic kidney disease.This review focuses on the current state of knowledge on EAT as a reliable new parameter for cardiovascular risk stratification in high risk populations.

Indexed as

AdipokinesAdipose TissueAdiposityAnimalsCardiovascular DiseasesHumansPericardiumPredictive Value of TestsPrognosisRisk AssessmentRisk FactorsSeverity of Illness IndexSignal TransductionAdipokinesCardiovascular riskChronic kidney diseaseCoronary artery calcificationCoronary artery diseaseEpicardial adipose tissue

Identifiers

PMID29704210
OpenAlexW2799407181

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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 Socratic graph.