Evidence map›Paper›PMID 26814014›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2016

Glucose uptake and lipid metabolism are impaired in epicardial adipose tissue from heart failure patients with or without diabetes.

Ana Burgeiro, Amelia Fuhrmann, Sam Cherian, Daniel Espinoza, Ivana Jarak, Rui A Carvalho, Marisa Loureiro, Miguel Patrício, Manuel Antunes, Eugénia Carvalho

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

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  16. Benefits of GLP-1 Mimetics on Epicardial Adiposity.Current medicinal chemistry · 2023
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  17. Review
  18. Epicardial adipose tissue in contemporary cardiology.Nature reviews. Cardiology · 2022 · on this map
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Ana BurgeiroCenter of Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal;
Amelia FuhrmannCenter of Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal;
Sam CherianFaculty of Integrative Sciences and Technology, Quest International University Perak, Perak, Malaysia;
Daniel EspinozaCenter of Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal;
Ivana JarakCenter of Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal;
Rui A CarvalhoCenter of Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal; Department of Life Sciences, Faculty of Sciences and Technology, University of Coimbra, Coimbra, Portugal; ecarvalh@cnc.uc.pt.
Marisa LoureiroLaboratory of Biostatistics and Medical Informatics, IBILI - Faculty of Medicine, University of Coimbra, Coimbra, Portugal;
Miguel PatrícioLaboratory of Biostatistics and Medical Informatics, IBILI - Faculty of Medicine, University of Coimbra, Coimbra, Portugal;
Manuel AntunesCardiothroracic Surgery Unit at the University Hospital of Coimbra, Coimbra, Portugal;
Eugénia CarvalhoCenter of Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal; Portuguese Diabetes Association, Lisbon, Portugal; Department of Geriatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas; and Arkansas Children's Hospital Research Institute, Little Rock, Arkansas.
University of Coimbra · PTQuest International University Perak · MYUniversity of Arkansas for Medical Sciences · US

Funding

RESOURCE CORE 3: ANALYTICAL COREP30AG028718 · NIA · UNIV OF ARKANSAS FOR MED SCIS · PI WEI, JEANNE Y · 2011 to 2015
$5.1M
Effects of amino acids on regional lipid metabolismR01AG033761 · NIA · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BORSHEIM, ELISABET · 2009 to 2013
$1.6M
NIA NIH HHS P30-AG-028718NIA NIH HHS R01-AG-033761
6 · The paper itself

Abstract

Type 2 diabetes mellitus is a complex metabolic disease, and cardiovascular disease is a leading complication of diabetes. Epicardial adipose tissue surrounding the heart displays biochemical, thermogenic, and cardioprotective properties. However, the metabolic cross-talk between epicardial fat and the myocardium is largely unknown. This study sought to understand epicardial adipose tissue metabolism from heart failure patients with or without diabetes. We aimed to unravel possible differences in glucose and lipid metabolism between human epicardial and subcutaneous adipocytes and elucidate the potential underlying mechanisms involved in heart failure. Insulin-stimulated [(14)C]glucose uptake and isoproterenol-stimulated lipolysis were measured in isolated epicardial and subcutaneous adipocytes. The expression of genes involved in glucose and lipid metabolism was analyzed by reverse transcription-polymerase chain reaction in adipocytes. In addition, epicardial and subcutaneous fatty acid composition was analyzed by high-resolution proton nuclear magnetic resonance spectroscopy. The difference between basal and insulin conditions in glucose uptake was significantly decreased (P= 0.006) in epicardial compared with subcutaneous adipocytes. Moreover, a significant (P< 0.001) decrease in the isoproterenol-stimulated lipolysis was also observed when the two fat depots were compared, and it was strongly correlated with lipolysis, lipid storage, and inflammation-related gene expression. Moreover, the fatty acid composition of these tissues was significantly altered by diabetes. These results emphasize potential metabolic differences between both fat depots in the presence of heart failure and highlight epicardial fat as a possible therapeutic target in situ in the cardiac microenvironment.

Indexed as

AdipocytesAdipose TissueAdrenergic beta-AgonistsAgedBlood GlucoseCarbon RadioisotopesCase-Control StudiesDiabetes Mellitus, Type 2Fatty AcidsFemaleGlucoseHeart FailureHumansHypoglycemic AgentsInsulinIsoproterenolAdrenergic beta-AgonistsBlood GlucoseCarbon RadioisotopesFatty AcidsGlucoseHypoglycemic AgentsInsulinIsoproterenoldiabetesepicardial adipose tissueglucose uptakeheart failurelipolysis

Identifiers

PMID26814014
PMCPMC4824138
OpenAlexW2264833793

What OpenQuestion holds

Textmetadata
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.