Evidence map›Paper›PMID 37697706›Full record

ArticleESC heart failure2023

Diverging role of epicardial adipose tissue across the entire heart failure spectrum.

Valentina A Rossi, Delia Nebunu, Thomas Haider, Natallia Laptseva, Matthias P Naegele, Frank Ruschitzka, Isabella Sudano, Andreas J Flammer

Open access · goldAbstract read
In one paragraph

Article in ESC heart failure, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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.

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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. 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

8 authors at 1 institution in 2 countries.

Valentina A RossiDepartment of Cardiology, University Heart Centre, University Hospital of Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.ORCID 0000-0001-9235-6597
Delia NebunuDepartment of Cardiology, University Heart Centre, University Hospital of Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.
Thomas HaiderDepartment of Cardiology, University Heart Centre, University Hospital of Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.
Natallia LaptsevaDepartment of Cardiology, University Heart Centre, University Hospital of Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.
Matthias P NaegeleDepartment of Cardiology, University Heart Centre, University Hospital of Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.
Frank RuschitzkaDepartment of Cardiology, University Heart Centre, University Hospital of Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.
Isabella SudanoDepartment of Cardiology, University Heart Centre, University Hospital of Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.
Andreas J FlammerDepartment of Cardiology, University Heart Centre, University Hospital of Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.ORCID 0000-0002-1373-0630
University of Zurich · CH

Funding

FreeNovation (FN22-422)
6 · The paper itself

Abstract

aimsEpicardial adipose tissue (EAT) is a metabolically highly active tissue modulating numerous pathophysiological processes. The aim of this study was to investigate the association between EAT thickness and endothelial function in patients with heart failure (HF) across the entire ejection fraction spectrum. METHODS AND

resultsA total of 258 patients with HF with an ejection fraction across the entire spectrum [HF with reduced ejection fraction (HFrEF), n = 168, age 60.6 ± 11.2 years; HF with preserved ejection fraction (HFpEF), n = 50, mean age 65.1 ± 11.9 years; HF with mildly reduced ejection fraction (HFmrEF), n = 32, mean age 65 ± 12] were included. EAT was measured with transthoracic echocardiography. Vascular function was assessed with flicker-light-induced vasodilation of retinal arterioles (FIDart%) and flow-mediated dilatation (FMD%) in conduit arteries. Patients with HFrEF have less EAT compared with patients with HFpEF (4.2 ± 2 vs. 5.3 ± 2 mm, respectively, P < 0.001). Interestingly, EAT was significantly associated with impaired microvascular function (FIDart%; r = -0.213, P = 0.012) and FMD% (r = -0.186, P = 0.022), even after multivariate correction for confounding factors (age, body mass index, hypertension, and diabetes; standardized regression coefficient (SRC) = -0.184, P = 0.049 for FIDart% and SRC = -0.178, P = 0.043 for FMD%) in HFrEF but not in HFpEF.

conclusionsAlthough less EAT is present in HFrEF than in HFpEF, only in HFrEF EAT is associated with vascular dysfunction. The diverging role of EAT in HF and its switch to a functionally deleterious tissue promoting HF progression provide the rationale to specifically target EAT, in particular in patients with reduced ejection fraction.

Indexed as

Diabetes MellitusHeart FailureVentricular Dysfunction, LeftAdipose TissueAgedHumansMiddle AgedPrognosisStroke VolumeEndothelial functionEpicardial adipose tissueFlow-mediated dilatationHeart failureRetinal vascular function

Identifiers

PMID37697706
PMCPMC10682858
OpenAlexW4386624733

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.