Evidence map›Paper›PMID 39045004›Full record

ArticleFrontiers in cardiovascular medicine2024

Genetic drivers of human plasma metabolites that determine mortality in heart failure patients with reduced ejection fraction.

Vandana Revathi Venkateswaran, Ruicong She, Hongsheng Gui, Jasmine A Luzum, Timothy D Bryson, Zack E Malouf, L Keoki Williams, Hani N Sabbah, Stephen J Gardell, David E Lanfear

Abstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

10 authors.

Vandana Revathi VenkateswaranCenter for Individualized and Genomic Medicine Research, Henry Ford Hospital, Detroit, MI, United States.
Ruicong SheDepartment of Public Health Science, Henry Ford Health, Detroit, MI, United States.
Hongsheng GuiCenter for Individualized and Genomic Medicine Research, Henry Ford Hospital, Detroit, MI, United States.
Jasmine A LuzumCenter for Individualized and Genomic Medicine Research, Henry Ford Hospital, Detroit, MI, United States.
Timothy D BrysonCenter for Individualized and Genomic Medicine Research, Henry Ford Hospital, Detroit, MI, United States.
Zack E MaloufCardiovascular Division, Department of Medicine, Henry Ford Hospital, Detroit, MI, United States.
L Keoki WilliamsCenter for Individualized and Genomic Medicine Research, Henry Ford Hospital, Detroit, MI, United States.
Hani N SabbahCardiovascular Division, Department of Medicine, Henry Ford Hospital, Detroit, MI, United States.
Stephen J GardellTranslational Research Institute, Advent Health, Orlando, FL, United States.
David E LanfearCenter for Individualized and Genomic Medicine Research, Henry Ford Hospital, Detroit, MI, United States.

Funding

Impact of Race and Genetic Factors on Beta-blocker Effectiveness in Heart FailureR01HL103871 · NHLBI · HENRY FORD HEALTH SYSTEM · PI LANFEAR, DAVID E · 2011 to 2015
$3.5M
Plasma Metabolomics and Myocardial Energetics in Heart FailureR01HL132154 · NHLBI · HENRY FORD HEALTH SYSTEM · PI LANFEAR, DAVID E, SABBAH, HANI N · 2017 to 2020
$3.1M
Precision Medicine for Heart Failure: The Role of Genomics in the Efficacy and Racial Disparity of Cornerstone PharmacotherapyK08HL146990 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUZUM, JASMINE A · 2019 to 2023
$772k
NHLBI NIH HHS K08 HL146990NHLBI NIH HHS R01 HL103871NHLBI NIH HHS R01 HL132154
6 · The paper itself

Abstract

Background: Heart failure with reduced ejection fraction (HFrEF) remains a significant public health issue, with the disease advancing despite neurohormonal antagonism. Energetic dysfunction is a likely contributor to residual disease progression, and we have previously reported a strong association of plasma metabolite profiles with survival among patients with HFrEF. However, the genetic and biologic mechanisms that underlie the metabolite-survival association in HFrEF were uncertain. Methods and results: We performed genetic mapping of the key metabolite parameters, followed by mediation analyses of metabolites and genotypes on survival, and genetic pathway analyses. Patients with HFrEF ( Conclusions: GWAS of key metabolites and survival along with FUMA pathway analysis revealed new candidate genes which unveiled molecular pathways that contribute to HF disease progression via metabolic and energetic abnormalities.

Indexed as

GWASheart failuremediation analysisplasma metabolitesQTL

Identifiers

PMID39045004
PMCPMC11263106

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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.