Evidence map›Paper›PMID 39611259›Full record

ArticleCirculation. Genomic and precision medicine2024

Polygenic Prediction of Recurrent Events After Early-Onset Myocardial Infarction.

Maddalena Ardissino, Elvezia Maria Paraboschi, Samuel A Lambert, Lois G Kim, Martin Kelemen, Giuseppe Maglietta, Antonio Crocamo, Giulia Magnani, Serena Bricoli, Luigi Vignali and 14 more

Abstract read
In one paragraph

Article in Circulation. Genomic and precision medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. What Should a Clinical Cardiologist Know About Cardiogenetics?Journal of the American Heart Association · 2025
    Review
  4. Review
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

24 authors.

Maddalena ArdissinoBritish Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care (M.A.,S.A.L., L.G.K., M.K., M.I., E.D.A., A.S.B.).ORCID 0000-0002-2654-8117
Elvezia Maria ParaboschiDepartment of Biomedical Sciences, Humanitas University (E.M.P., R.A.).
Samuel A LambertBritish Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care (M.A.,S.A.L., L.G.K., M.K., M.I., E.D.A., A.S.B.).ORCID 0000-0001-8222-008X
Lois G KimBritish Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care (M.A.,S.A.L., L.G.K., M.K., M.I., E.D.A., A.S.B.).ORCID 0000-0002-4552-3820
Martin KelemenBritish Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care (M.A.,S.A.L., L.G.K., M.K., M.I., E.D.A., A.S.B.).ORCID 0000-0002-4050-1817
Giuseppe MagliettaClinical and Epidemiological Research Unit (G. Maglietta), University Hospital of Parma.ORCID 0000-0003-4497-1872
Antonio CrocamoDepartment of Cardiology (A.C., G. Magnani, S.B., L.V., G.N.), University Hospital of Parma.
Giulia MagnaniDepartment of Cardiology (A.C., G. Magnani, S.B., L.V., G.N.), University Hospital of Parma.
Serena BricoliDepartment of Cardiology (A.C., G. Magnani, S.B., L.V., G.N.), University Hospital of Parma.ORCID 0000-0002-6832-8243
Luigi VignaliDepartment of Cardiology (A.C., G. Magnani, S.B., L.V., G.N.), University Hospital of Parma.
Giampaolo NiccoliDepartment of Cardiology (A.C., G. Magnani, S.B., L.V., G.N.), University Hospital of Parma.
Marco TubaroDivision of Cardiology, San Filippo Neri Hospital, Rome, Italy (M.T.).ORCID 0000-0003-1702-2401
Libor PastikaNational Heart and Lung Research Institute (M.A.,L.P., A.S., F.S.N.).
Arunashis SauNational Heart and Lung Research Institute (M.A.,L.P., A.S., F.S.N.).ORCID 0000-0002-0204-7078
Fu Siong NgNational Heart and Lung Research Institute (M.A.,L.P., A.S., F.S.N.).ORCID 0000-0002-8681-4368
Antonio de MarvaoMedical Research Council-London Institute of Medical Sciences, Imperial College London, United Kingdom (M.A.,A.M.).ORCID 0000-0001-9095-5887
Michael C HonigbergProgram in Medical and Population Genetics, Broad Institute of Harvard & MIT, Cambridge (M.C.H., P.N.).ORCID 0000-0001-8630-5021
Pradeep NatarajanProgram in Medical and Population Genetics, Broad Institute of Harvard & MIT, Cambridge (M.C.H., P.N.).ORCID 0000-0001-8402-7435
Adam J NelsonAdelaide Medical School, University of Adelaide (A.J.N.).ORCID 0000-0003-0990-2548
Michael InouyeBritish Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care (M.A.,S.A.L., L.G.K., M.K., M.I., E.D.A., A.S.B.).ORCID 0000-0001-9413-6520
Emanuele Di AngelantonioBritish Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care (M.A.,S.A.L., L.G.K., M.K., M.I., E.D.A., A.S.B.).ORCID 0000-0001-8776-6719
Rosanna AsseltaDepartment of Biomedical Sciences, Humanitas University (E.M.P., R.A.).ORCID 0000-0001-5351-0619
Diego Ardissino *Department of Medicine and Surgery, University of Parma (D.A.).ORCID 0000-0003-0410-3528
Adam S Butterworth *British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care (M.A.,S.A.L., L.G.K., M.K., M.I., E.D.A., A.S.B.).ORCID 0000-0002-6915-9015

Funding

Clonal hematopoiesis as a mediator of cardiovascular disease in women with premature menopauseK08HL166687 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI HONIGBERG, MICHAEL · 2023 to 2025
$507k
British Heart Foundation RG/18/13/33946British Heart Foundation RG/F/22/110078NHLBI NIH HHS K08 HL166687
6 · The paper itself

Abstract

backgroundMyocardial infarction (MI) is a complex disease caused by both lifestyle and genetic factors. This study aims to investigate the predictive value of genetic risk, in addition to traditional cardiovascular risk factors, for recurrent events following early-onset MI.

methodsThe Italian Genetic Study of Early-Onset Myocardial Infarction is a cohort study enrolling patients with MI before 45 years. Monogenic variants causing familial hypercholesterolemia were identified, and a coronary artery disease polygenic score (PGS) was calculated. Ten-fold cross-validated Cox proportional hazards models were fitted sequentially including all clinical variables, the PGS, and monogenic variants on the composite outcome of cardiovascular death, recurrent MI, stroke, or revascularization.

resultsDuring a 19.9-year follow-up, 847 (50.7%) patients experienced recurrent events. Each 1-SD higher PGS was associated with a 21% higher hazard of recurrent events (hazard ratio, 1.21 [95% CI, 1.13-1.31];

conclusionsWhen compared with other clinical risk factors, PGS was the strongest predictor of event recurrence among patients with an early-onset MI. Though the discriminative power of recurrent event prediction in this cohort was modest, the addition of PGS significantly improved discrimination.

Indexed as

Multifactorial InheritanceMyocardial InfarctionRecurrenceAdultAge of OnsetCohort StudiesCoronary Artery DiseaseFemaleFollow-Up StudiesGenetic Predisposition to DiseaseHumansHyperlipoproteinemia Type IIMaleMiddle AgedProportional Hazards ModelsRisk Factorscardiovascular diseasescoronary artery diseasegenetic risk scoregeneticsheart disease risk factors

Identifiers

PMID39611259
PMCPMC11651354

What OpenQuestion 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 OpenQuestion graph.