Evidence map›Paper›PMID 38225249›Full record

ArticleNature communications2024

Large scale plasma proteomics identifies novel proteins and protein networks associated with heart failure development.

Amil M Shah, Peder L Myhre, Victoria Arthur, Pranav Dorbala, Humaira Rasheed, Leo F Buckley, Brian Claggett, Guning Liu, Jianzhong Ma, Ngoc Quynh Nguyen and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
32.5field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
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  15. Decoding the Heart Failure Peptidome.Circulation. Heart failure · 2026
    Article
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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

22 authors at 8 institutions in 2 countries.

Amil M ShahDivision of Cardiology, University of Texas Southwestern Medical Center, Dallas, TX, USA. Amil.Shah@utsouthwestern.edu.ORCID 0000-0003-1056-4451
Peder L MyhreAkershus University Hospital and K.G. Jebsen Center for Cardiac Biomarkers, University of Oslo, Oslo, Norway.
Victoria ArthurDivision of Cardiology, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0003-2760-5053
Pranav DorbalaDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Humaira RasheedAkershus University Hospital and K.G. Jebsen Center for Cardiac Biomarkers, University of Oslo, Oslo, Norway.ORCID 0000-0002-3331-5864
Leo F BuckleyDepartment of Pharmacy, Brigham and Women's Hospital, Boston, MA, USA.
Brian ClaggettDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Guning LiuDepartment of Epidemiology, Human Genetics, and Environmental Sciences, University of Texas Health Sciences Center at Houston, Houston, TX, USA.
Jianzhong MaDepartment of Epidemiology, Human Genetics, and Environmental Sciences, University of Texas Health Sciences Center at Houston, Houston, TX, USA.
Ngoc Quynh NguyenDepartment of Epidemiology, Human Genetics, and Environmental Sciences, University of Texas Health Sciences Center at Houston, Houston, TX, USA.
Kunihiro MatsushitaDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Chiadi NdumeleDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Adrienne TinUniversity of Mississippi Medical Center, Jackson, MS, USA.ORCID 0000-0002-4207-5866
Kristian HveemDepartment of Public Health and Nursing, HUNT Research Center, Norwegian University of Science and Technology, Trondheim, Norway.
Christian JonassonDepartment of Public Health and Nursing, HUNT Research Center, Norwegian University of Science and Technology, Trondheim, Norway.ORCID 0000-0002-7694-6025
Håvard DalenDepartment of Circulation and Medical Imaging, Norwegian University of Science and Technology, Trondheim, Norway.
Eric BoerwinkleDepartment of Epidemiology, Human Genetics, and Environmental Sciences, University of Texas Health Sciences Center at Houston, Houston, TX, USA.
Ron C HoogeveenDivision of Cardiology, Baylor College of Medicine, Houston, TX, USA.
Christie BallantyneDivision of Cardiology, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0002-6432-1730
Josef CoreshDepartments of Medicine and Population Health, NYU Langone Health, New York, NY, USA.ORCID 0000-0002-4598-0669
Torbjørn OmlandAkershus University Hospital and K.G. Jebsen Center for Cardiac Biomarkers, University of Oslo, Oslo, Norway.
Bing YuDepartment of Epidemiology, Human Genetics, and Environmental Sciences, University of Texas Health Sciences Center at Houston, Houston, TX, USA.ORCID 0000-0003-4818-1077
Brigham and Women's Hospital · USThe University of Texas Health Science Center at Houston · USNorwegian University of Science and Technology · NOUniversity of Oslo · NOBaylor College of Medicine · USJohns Hopkins University · USJackson Memorial Hospital · USNYU Langone Health · US

Funding

Mapping the Progression to HFpEF in the Elderly through Longitudinal Changes in Cardiac FunctionR01HL135008 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI Amil M Shah · 2017 to 2026
$11.5M
Proteomic signatures to identifypathways underlying the progression toheart failureR01HL148218 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI SHAH, AMIL M, YU, BING · 2020 to 2023
$3.4M
Mentoring patient-oriented research in deep phenotyping of cardiac function for heart failure preventionK24HL152008 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI SHAH, AMIL M · 2020 to 2024
$608k
NHLBI NIH HHS R01 HL148218
6 · The paper itself

Abstract

Heart failure (HF) causes substantial morbidity and mortality but its pathobiology is incompletely understood. The proteome is a promising intermediate phenotype for discovery of novel mechanisms. We measured 4877 plasma proteins in 13,900 HF-free individuals across three analysis sets with diverse age, geography, and HF ascertainment to identify circulating proteins and protein networks associated with HF development. Parallel analyses in Atherosclerosis Risk in Communities study participants in mid-life and late-life and in Trøndelag Health Study participants identified 37 proteins consistently associated with incident HF independent of traditional risk factors. Mendelian randomization supported causal effects of 10 on HF, HF risk factors, or left ventricular size and function, including matricellular (e.g. SPON1, MFAP4), senescence-associated (FSTL3, IGFBP7), and inflammatory (SVEP1, CCL15, ITIH3) proteins. Protein co-regulation network analyses identified 5 modules associated with HF risk, two of which were influenced by genetic variants that implicated trans hotspots within the VTN and CFH genes.

Indexed as

AtherosclerosisHeart FailureCarrier ProteinsExtracellular Matrix ProteinsGlycoproteinsHumansPhenotypeProteomicsRisk FactorsCarrier ProteinsExtracellular Matrix ProteinsGlycoproteinsMFAP4 protein, human

Identifiers

PMID38225249
PMCPMC10789789
OpenAlexW4390876420

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.