Evidence map›Paper›PMID 32627354›Full record

ArticleESC heart failure2020

Relation between plasma ceramides and cardiovascular death in chronic heart failure: A subset analysis of the GISSI-HF trial.

Giovanni Targher, Gianluigi Lunardi, Alessandro Mantovani, Jennifer Meessen, Stefano Bonapace, Pier Luigi Temporelli, Enrico Nicolis, Deborah Novelli, Antonio Conti, Luigi Tavazzi and 2 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in ESC heart failure, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT00336336. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 27% 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.

NCT00336336 phase3completed

A Large Scale Clinical Trial Testing the Effects of n-3 PUFA and Rosuvastatin on Mortality-Morbidity of Patients With Symptomatic Congestive Heart Failure

Ran2002Enrolled6,975Registered outcomes10Posted comparisons0ConditionsHeart FailureArmsn-3 PUFA, Placebo, Rosuvastatin
PMID 18757089PMID 15302013PMID 18757090other papers from this trial
Open the trial in the graph
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. The role of sphingolipids in heart failure.European heart journal open · 2025
    Review
  8. Review
  9. Review
  10. Article
  11. Circulating sphingolipids in heart failure.Frontiers in cardiovascular medicine · 2023
    Review
  12. Article
  13. Review
  14. Review
  15. Sphingolipid metabolism and signaling in cardiovascular diseases.Frontiers in cardiovascular medicine · 2022
    Review
  16. Article
  17. Review
  18. 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

12 authors at 6 institutions in 2 countries.

Giovanni TargherDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University and Azienda Ospedaliera Universitaria Integrata of Verona, Piazzale Stefani, 1, Verona, 37126, Italy.ORCID https://orcid.org/0000-0002-4325-3900
Gianluigi LunardiMedical Analysis Laboratory, 'IRCCS Sacro Cuore-Don Calabria' Hospital, Negrar, Italy.
Alessandro MantovaniDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University and Azienda Ospedaliera Universitaria Integrata of Verona, Piazzale Stefani, 1, Verona, 37126, Italy.
Jennifer MeessenDepartment of Cardiovascular Medicine, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Stefano BonapaceDivision of Cardiology, 'IRCCS Sacro Cuore-Don Calabria' Hospital, Negrar, Italy.
Pier Luigi TemporelliDivision of Cardiology, Istituti Clinici Scientifici Maugeri, IRCCS, Veruno, Italy.
Enrico NicolisDepartment of Cardiovascular Medicine, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Deborah NovelliDepartment of Cardiovascular Medicine, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Antonio ContiMedical Analysis Laboratory, 'IRCCS Sacro Cuore-Don Calabria' Hospital, Negrar, Italy.
Luigi TavazziMaria Cecilia Hospital, GVM Care & Research, Cotignola, Italy.
Aldo Pietro MaggioniANMCO Research Center, Florence, Italy.
Roberto LatiniDepartment of Cardiovascular Medicine, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Mario Negri Institute for Pharmacological Research · ITOspedale Sacro Cuore Don Calabria · ITAzienda Ospedaliera Universitaria Integrata Verona · ITAssociazione Nazionale Medici Cardiologi Ospedalieri · ITIstituti Clinici Scientifici Maugeri · ITMaria Cecilia Hospital · IT

Funding

AstraZenecaPfizerSigma TauUniversity of Verona School of Medicine, Italy
6 · The paper itself

Abstract

aimsCeramides exert several biological activities that may contribute to the pathophysiology of cardiovascular disease and heart failure (HF). The association between plasma levels of distinct ceramides (that have been previously associated with increased cardiovascular risk) and cardiovascular mortality in patients with chronic HF has received little attention. METHODS AND

resultsIn a post hoc ancillary analysis of the Gruppo Italiano per lo Studio della Sopravvivenza nella Insufficienza Cardiaca-Heart Failure (GISSI-HF; NCT00336336) trial, we randomly selected a sample of 200 ambulatory patients with chronic HF who died due to cardiovascular causes and 200 patients who were alive at the end of the trial (after a median follow-up period of 3.9 years). We measured baseline plasma concentrations of six previously identified high-risk ceramide species [Cer(d18:1/16:0), Cer(d18:1/18:0), Cer(d18:1/20:0), Cer(d18:1/22:0), Cer(d18:1/24:0), and Cer(d18:1/24:1) and their individual plasma ratios with Cer(d18:1/24:0)]. Patients who died due to cardiovascular causes had significantly (P < 0.05 or less) higher levels of plasma Cer(d18:1/16:0) and Cer(d18:1/24:1), but lower levels of plasma Cer(d18:1/22:0) and Cer(d18:1/24:0) than had those who did not. All plasma ratios of each ceramide with Cer(d18:1/24:0) were significantly higher in patients who died due to cardiovascular causes. In Cox regression analyses, all five plasma ratios of each ceramide with Cer(d18:1/24:0) were significantly associated with a greater risk of cardiovascular mortality (with unadjusted hazard ratios ranging from 1.23 to 1.59; P < 0.001 or less). These significant associations were attenuated after adjustment for multiple established risk factors, New York Heart Association functional class, left ventricular ejection fraction, use of medications, plasma pentraxin-3 levels, and, especially, plasma N-terminal pro-brain natriuretic peptide (NT-proBNP) levels. When we applied a Bonferroni correction for multiple comparisons (using a P-threshold 0.05/5 ceramide ratios = 0.01), none of the five plasma ratios of each ceramide with Cer(d18:1/24:0) remained statistically associated with the risk of cardiovascular mortality (with adjusted hazard ratios ranging from 1.10 to 1.23).

conclusionsHigher levels of specific plasma ceramides [especially when used in ratios with Cer(d18:1/24:0)] are associated with increased cardiovascular mortality in ambulatory patients with chronic HF. However, these associations are weakened after adjustment for established cardiovascular risk factors, medication use, and plasma NT-proBNP concentrations.

Indexed as

Cardiovascular mortalityCeramidesHeart failureRisk factors

Identifiers

PMID32627354
PMCPMC7754905
OpenAlexW3039187968

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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 OpenQuestion graph.