Evidence map›Paper›PMID 38613511›Full record

Observational studyCardiovascular research2024

Blood-based cardiometabolic phenotypes in atrial fibrillation and their associated risk: EAST-AFNET 4 biomolecule study.

Larissa Fabritz, Winnie Chua, Victor R Cardoso, Christoph Al-Taie, Katrin Borof, Anna Suling, Linda Krause, Shinwan Kany, Christina Magnussen, Karl Wegscheider and 12 more

Open access · hybridAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Cardiovascular research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Interactions of blood biomolecules with early rhythm control in atrial fibrillation patients: exploratory analysis of the EAST-AFNET 4 biomolecule study.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2026
    Trial
  3. Prevalence and severity of atrial cardiomyopathy in patients with recently diagnosed atrial fibrillation and stroke risk factors and its association with early rhythm control: a secondary analysis of EAST-AFNET 4.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2025
    Trial
  4. Trial
  5. ImpairedERJ open research · 2026
    Article
  6. Comprehensive assessment of novel cardiovascular biomarkers in AF.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2026
    Article
  7. Observational
  8. Article
  9. Review
  10. Transforming atrial fibrillation management by targeting comorbidities and reducing atrial fibrillation burden: the 10th AFNET/EHRA consensus conference.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2025
    Article
  11. A novel technique for vein of Marshall blood sampling and its application in assessing atrial remodeling in atrial fibrillation.Clinical research in cardiology : official journal of the German Cardiac Society · 2025
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  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

22 authors at 9 institutions in 4 countries.

Larissa FabritzDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246 Hamburg, Germany.ORCID 0000-0002-9241-1733
Winnie ChuaInstitute of Cardiovascular Sciences, University of Birmingham, Wolfson Drive, Birmingham, UK.ORCID 0000-0002-6747-8813
Victor R CardosoInstitute of Cardiovascular Sciences, University of Birmingham, Wolfson Drive, Birmingham, UK.ORCID 0000-0002-9588-6304
Christoph Al-TaieDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246 Hamburg, Germany.ORCID 0000-0001-7088-3943
Katrin BorofDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246 Hamburg, Germany.
Anna SulingInstitute of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-8537-1948
Linda KrauseInstitute of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-8490-5717
Shinwan KanyDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246 Hamburg, Germany.ORCID 0000-0001-8113-733X
Christina MagnussenDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246 Hamburg, Germany.ORCID 0000-0002-5102-0955
Karl WegscheiderInstitute of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-2974-3142
Guenter BreithardtUniversity Hospital Münster, Münster, Albert-Schweitzer-Straße 1A, 48149 Münster, Germany.ORCID 0000-0001-7574-8900
Harry J G M CrijnsDepartment of Cardiology, University Hospital Maastricht, Maastricht, The Netherlands.ORCID 0000-0003-1073-5337
A John CammClinical Sciences, St George´s University, London, UK.ORCID 0000-0002-2536-2871
George GkoutosInstitute of Cardiovascular Sciences, University of Birmingham, Wolfson Drive, Birmingham, UK.ORCID 0000-0002-2061-091X
Patrick T EllinorCardiovascular Disease Initiative, The Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0002-2067-0533
Andreas GoetteVincenz-Krankenhaus, Am Busdorf 2, 33098 Paderborn, Germany.ORCID 0000-0002-8223-7209
Ulrich SchottenAFNET, Münster, Germany.ORCID 0000-0003-1532-3315
Ursula-Henrike Wienhues-ThelenRoche Diagnostics, Nonnenwald 2, 82377 Penzberg, Germany.
Tanja ZellerDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246 Hamburg, Germany.ORCID 0000-0003-3379-2641
Renate B SchnabelDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246 Hamburg, Germany.
Antonia ZapfInstitute of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-8467-0508
Paulus KirchhofDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246 Hamburg, Germany.ORCID 0000-0002-1881-0197
Universität Hamburg · DEUniversity of Birmingham · GBBroad Institute · USMaastricht University · NLMaastricht University Medical Centre · NLRoche Pharma AG (Germany) · DESt George's, University of London · GBSt. Vincenz-Krankenhaus Limburg · DEUniversity Hospital Münster · DE

Funding

IDENTIFICATION OF COMMON GENETIC VARIANTS FOR ATRIAL FIBRILLATION AND PR INTERVALR01HL092577 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI BENJAMIN, EMELIA J., ELLINOR, PATRICK THOMAS · 2009 to 2025
$20.6M
Using Electrocardiogram Genetics to Inform Arrhythmia RiskR01HL157635 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ELLINOR, PATRICK THOMAS, MIRSHAHI, TOORAJ · 2022 to 2025
$2.9M
AFNETAmerican Heart Association 18SFRN34230127BMBFBritish Heart Foundation PG/20/22/35093CATCH-MECATCH-ME EU 965286 (Deutsche Stiftung für HerzforschungDr Rolf M. Schwiete StiftungDutch Heart Foundation CVON2014-09DZHKEHRAERACoSysMed3 031L0239European Research CouncilEuropean Union's Horizon 2020 research and innovation programme 648131European Union's Horizon 2020 research and innovation programme 847770European Union's Horizon Europe research and innovation programme 101095480German Heart Foundation EU 633196German Ministry of Education and ResearchGerman Ministry of Education and Research FKZ 81X2800182German Ministry of Research and Education BMBF 01ZX1408AGerman Research Foundation Ki 509167694Leducq Foundation EU 633196Loewenstein MedicalMAESTRIANDDNHLBI NIH HHS R01 HL157635NIH HHS RO1HL092577promotion of women scientists programme FKZ 81X3710112SanofiSt Jude Medical-Abbott
6 · The paper itself

Abstract

aimsAtrial fibrillation (AF) and concomitant cardiometabolic disease processes interact and combine to lead to adverse events, such as stroke, heart failure, myocardial infarction, and cardiovascular death. Circulating biomolecules provide quantifiable proxies for cardiometabolic disease processes. The aim of this study was to test whether biomolecule combinations can define phenotypes in patients with AF. METHODS AND

resultsThis pre-specified analysis of the EAST-AFNET 4 biomolecule study assigned patients to clusters using polytomous variable latent-class analysis based on baseline concentrations of 13 precisely quantified biomolecules potentially reflecting ageing, cardiac fibrosis, metabolic dysfunction, oxidative stress, cardiac load, endothelial dysfunction, and inflammation. In each cluster, rates of cardiovascular death, stroke, or hospitalization for heart failure or acute coronary syndrome, the primary outcome of EAST-AFNET 4, were calculated and compared between clusters over median 5.1 years follow-up. Findings were independently validated in a prospective cohort of 748 patients with AF (BBC-AF; median follow-up 2.9 years).Unsupervised biomolecule analysis assigned 1586 patients (71 years old, 46% women) into four clusters. The highest risk cluster was dominated by elevated bone morphogenetic protein 10, insulin-like growth factor-binding protein 7, N-terminal pro-B-type natriuretic peptide, angiopoietin 2, and growth differentiation factor 15. Patients in the lowest risk cluster showed low concentrations of these biomolecules. Two intermediate-risk clusters differed by high or low concentrations of C-reactive protein, interleukin-6, and D-dimer. Patients in the highest risk cluster had a five-fold higher cardiovascular event rate than patients in the low-risk cluster. Early rhythm control was effective across clusters (Pinteraction = 0.63). Sensitivity analyses and external validation in BBC-AF replicated clusters and risk gradients.

conclusionBiomolecule concentrations identify cardiometabolic subphenotypes in patients with AF at high and low cardiovascular risk.

Indexed as

Atrial FibrillationBiomarkersCardiometabolic Risk FactorsPhenotypeAgedAged, 80 and overEuropeFemaleHumansMaleMiddle AgedPredictive Value of TestsPrognosisProspective StudiesRisk AssessmentTime FactorsBiomarkersAtrial fibrillationBiomoleculesHeart failureMetabolismRisk predictionStroke

Identifiers

PMID38613511
PMCPMC11218688
OpenAlexW4394786441

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.