Evidence map›Paper›PMID 36217578›Full record

ArticleESC heart failure2023

Metabolomics implicate eicosanoids in severe functional mitral regurgitation.

Thomas M Hofbauer, Klaus Distelmaier, Besnik Muqaku, Georg Spinka, Veronika Seidl, Henrike T Arfsten, Gerhard Hagn, Samuel Meier-Menches, Philipp E Bartko, Noemi Pavo and 9 more

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 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Recent advances in omics-based research of mitral valve disease.Frontiers in cardiovascular medicine · 2026
    Review
  3. Article
  4. Review
  5. 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

19 authors at 3 institutions in 2 countries.

Thomas M HofbauerDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.ORCID https://orcid.org/0000-0001-5324-6336
Klaus DistelmaierDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.
Besnik MuqakuInstitute of Analytical Chemistry, University of Vienna, Vienna, Austria.
Georg SpinkaDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.
Veronika SeidlDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.
Henrike T ArfstenDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.
Gerhard HagnInstitute of Analytical Chemistry, University of Vienna, Vienna, Austria.
Samuel Meier-MenchesInstitute of Analytical Chemistry, University of Vienna, Vienna, Austria.
Philipp E BartkoDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.
Noemi PavoDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.
Matthias HokeDepartment of Angiology, Internal Medicine II, Medical University of Vienna, Vienna, Austria.
Suriya PrausmuellerDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.
Gregor HeitzingerDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.
Dietmar PilsJoint Metabolome Facility, University of Vienna and Medical University of Vienna, Vienna, Austria.
Irene M LangDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.
Christian HengstenbergDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.
Martin P HülsmannDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.
Christopher GernerJoint Metabolome Facility, University of Vienna and Medical University of Vienna, Vienna, Austria.
Georg GoliaschDepartment of Cardiology, Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, A-1090, Vienna, Austria.
Medical University of Vienna · ATUniversity of Vienna · ATDeutsches Herzzentrum der Charité · DE

Funding

Austrian Science Fund KLI-818BAustrian Science Fund FWF KLI 818
6 · The paper itself

Abstract

aimsSecondary, or functional, mitral regurgitation (FMR) was recently recognized as a separate clinical entity, complicating heart failure with reduced ejection fraction (HFrEF) and entailing particularly poor outcome. Currently, there is a lack of targeted therapies for FMR due to the fact that pathomechanisms leading to FMR progression are incompletely understood. In this study, we sought to perform metabolomic profiling of HFrEF patients with severe FMR, comparing results to patients with no or mild FMR. METHODS AND

resultsTargeted plasma metabolomics and untargeted eicosanoid analyses were performed in samples drawn from HFrEF patients (n = 80) on optimal guideline-directed medical therapy. Specifically, 17 eicosanoids and 188 metabolites were analysed. Forty-seven patients (58.8%) had severe FMR, and 33 patients (41.2%) had no or non-severe FMR. Comparison of eicosanoid levels between groups, accounting for age, body mass index, and sex, revealed significant up-regulation of six eicosanoids (11,12-EET, 13(R)-HODE, 12(S)-HETE, 8,9-DiHETrE, metPGJ2, and 20-HDoHE) in severe FMR patients. Metabolites did not differ significantly. In patients with severe FMR, but not in those without severe FMR, levels of 8,9-DiHETrE above a cut-off specified by receiver-operating characteristic analysis independently predicted all-cause mortality after a median follow-up of 43 [interquartile range 38, 48] months [hazard ratio 12.488 (95% confidence interval 3.835-40.666), P < 0.0001].

conclusionsWe report the up-regulation of various eicosanoids in patients with severe FMR, with 8,9-DiHETrE appearing to predict mortality. Our observations may serve as a nucleus for further investigations into the causes and consequences of metabolic derangements in this important valvular abnormality.

Indexed as

Heart FailureMitral Valve InsufficiencyHumansPrognosisStroke VolumeEicosanoidsFunctional mitral regurgitationHeart failureMetabolomics

Identifiers

PMID36217578
PMCPMC9871691
OpenAlexW4304166229

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.