Evidence map›Paper›PMID 34463125›Full record

Trial reportCirculation. Genomic and precision medicine2021

Predictive Accuracy of a Clinical and Genetic Risk Model for Atrial Fibrillation.

Shaan Khurshid, Nina Mars, Christopher M Haggerty, Qiuxi Huang, Lu-Chen Weng, Dustin N Hartzel, Regeneron Genetics Center, Kathryn L Lunetta, Jeffrey M Ashburner, Christopher D Anderson and 7 more

Open access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Circulation. Genomic and precision medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

27 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  16. Innovative approaches to atrial fibrillation prediction: should polygenic scores and machine learning be implemented in clinical practice?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 · 2024
    Review
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  20. Advances in basic and translational research in atrial fibrillation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    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

17 authors at 7 institutions in 3 countries.

Shaan KhurshidDivision of Cardiology (S.K.), Massachusetts General Hospital, Boston.ORCID 0000-0002-2840-4539
Nina MarsInstitute for Molecular Medicine Finland, FIMM, HiLIFE (N.M., S.R.), University of Helsinki, Finland.ORCID 0000-0001-6113-8247
Christopher M HaggertyHeart Institute (C.M.H., B.K.F.) and Informatics, Geisinger, Danville, PA.ORCID 0000-0001-6113-8247
Qiuxi HuangDepartment of Biostatistics (Q.H., K.L.L, L.T.), Boston University School of Medicine.ORCID 0000-0001-6113-8247
Lu-Chen WengCardiovascular Research Center (S.K., L.-C.W., P.T.E., S.A.L.), Massachusetts General Hospital, Boston.
Dustin N HartzelPhenomic Analytics and Clinical Data Core, Geisinger Health, Danville, PA (D.N.H.).ORCID 0000-0002-9057-2832
Regeneron Genetics Center
Kathryn L LunettaDepartment of Biostatistics (Q.H., K.L.L, L.T.), Boston University School of Medicine.ORCID 0000-0002-9268-810X
Jeffrey M AshburnerDivision of General Internal Medicine (J.M.A.), Massachusetts General Hospital, Boston.ORCID 0000-0002-5600-3492
Christopher D AndersonHenry and Allison McCance Center for Brain Health (C.D.A.), Massachusetts General Hospital, Boston.ORCID 0000-0002-0053-2002
Emelia J BenjaminSections of Preventive Medicine and Cardiovascular Medicine, Department of Medicine (E.J.B.), Boston University School of Medicine.ORCID 0000-0003-4076-2336
Veikko SalomaaRegeneron Pharmaceuticals, Tarrytown, NY. Finnish Institute for Health and Welfare, Helsinki, Finland (V.S.).ORCID 0000-0001-7563-5324
Patrick T EllinorCardiovascular Research Center (S.K., L.-C.W., P.T.E., S.A.L.), Massachusetts General Hospital, Boston.ORCID 0000-0002-2067-0533
Brandon K FornwaltHeart Institute (C.M.H., B.K.F.) and Informatics, Geisinger, Danville, PA.ORCID 0000-0001-6113-8247
Samuli RipattiInstitute for Molecular Medicine Finland, FIMM, HiLIFE (N.M., S.R.), University of Helsinki, Finland.ORCID 0000-0001-6113-8247
Ludovic TrinquartDepartment of Biostatistics (Q.H., K.L.L, L.T.), Boston University School of Medicine.ORCID 0000-0002-3028-4900
Steven A LubitzCardiovascular Research Center (S.K., L.-C.W., P.T.E., S.A.L.), Massachusetts General Hospital, Boston.ORCID 0000-0002-9599-4866
Broad Institute · USBoston University · USGeisinger Medical Center · USGeisinger Health System · USInstitute for Molecular Medicine Finland · FIMassachusetts General Hospital · USRegeneron (United States) · US

Funding

Ethnic/Racial Variation in Intracerebral Hemorrhage (ERICH)U01NS069763 · NINDS · UNIVERSITY OF CINCINNATI · PI ANDERSON, CHRISTOPHER DAVID, DEMEL, STACIE · 2010 to 2024
$34.2M
FRAMINGHAM HEART STUDY - YEAR 5 EXAM75N92019D00031 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · 2019 to 2024
$29.8M
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
ConProject-006U54HL120163 · NHLBI · AMERICAN HEART ASSOCIATION · PI BHATNAGAR, ARUNI, ROBERTSON, ROSE MARIE · 2018 to 2022
$18.8M
MULTIDISCIPLINARY RESEARCH TRAINING IN CARDIOLOGYT32HL007208 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Patrick Thomas Ellinor, David E Sosnovik · 1985 to 2026
$16.1M
Sequencing Annotation and Functional Analysis in Risk of Intracerebral HemorrhageR01NS103924 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI ANDERSON, CHRISTOPHER DAVID · 2018 to 2022
$3.4M
Genomics of Cardiac ArrhythmiasR01HL139731 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ELLINOR, PATRICK THOMAS · 2018 to 2022
$3.3M
AFGen Consortium: Atrial Fibrillation Genomics to Functional AnalysesR01HL128914 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BENJAMIN, EMELIA J., ELLINOR, PATRICK THOMAS · 2015 to 2018
$3.1M
FHS-NEXT - Framingham Novel EXam using TechnologyR01HL141434 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BENJAMIN, EMELIA J., MCMANUS, DAVID D. · 2019 to 2022
$2.5M
Determining the Role of the Potassium Channel, KCNN3, in Atrial FibrillationR01HL104156 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ELLINOR, PATRICK THOMAS · 2010 to 2013
$2.1M
Mentoring in Arrhythmia ResearchK24HL105780 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ELLINOR, PATRICK THOMAS · 2011 to 2020
$1.2M
THE FRAMINGHAM HEART STUDY-N01HC25195-268025195-268025195N01HC025195 · HC · TRUSTEES OF BOSTON UNIVERSITY · PI WOLF, PHILIP A · 2002 to 2006
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American Heart Association-American Stroke Association 18SFRN34150007American Heart Association-American Stroke Association 18SFRN34250007British Heart Foundation CH/1996001/9454Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NHLBI NIH HHS 75N92019D00031NHLBI NIH HHS HHSN268201500001CNHLBI NIH HHS HHSN268201500001INHLBI NIH HHS K24 HL105780NHLBI NIH HHS N01 HC025195NHLBI NIH HHS R01 HL092577NHLBI NIH HHS R01 HL104156NHLBI NIH HHS R01 HL128914NHLBI NIH HHS R01 HL139731NHLBI NIH HHS R01 HL141434NHLBI NIH HHS T32 HL007208NHLBI NIH HHS U54 HL120163NINDS NIH HHS R01 NS103924NINDS NIH HHS U01 NS069763
6 · The paper itself

Abstract

backgroundAtrial fibrillation (AF) risk estimation using clinical factors with or without genetic information may identify AF screening candidates more accurately than the guideline-based age threshold of ≥65 years.

methodsWe analyzed 4 samples across the United States and Europe (derivation: UK Biobank; validation: FINRISK, Geisinger MyCode Initiative, and Framingham Heart Study). We estimated AF risk using the CHARGE-AF (Cohorts for Heart and Aging Research in Genomic Epidemiology AF) score and a combination of CHARGE-AF and a 1168-variant polygenic score (Predict-AF). We compared the utility of age, CHARGE-AF, and Predict-AF for predicting 5-year AF by quantifying discrimination and calibration.

resultsAmong 543 093 individuals, 8940 developed AF within 5 years. In the validation sets, CHARGE-AF (C index range, 0.720-0.824) and Predict-AF (0.749-0.831) had largely comparable discrimination, both favorable to continuous age (0.675-0.801). Calibration was similar using CHARGE-AF (slope range, 0.67-0.87) and Predict-AF (0.65-0.83). Net reclassification improvement using Predict-AF versus CHARGE-AF was modest (net reclassification improvement range, 0.024-0.057) but more favorable among individuals aged <65 years (0.062-0.11). Using Predict-AF among 99 530 individuals aged ≥65 years across each sample, 70 849 had AF risk <5%, of whom 69 067 (97.5%) did not develop AF, whereas 28 681 had AF risk ≥5%, of whom 2264 (7.9%) developed AF. Of 11 379 individuals aged <65 years with AF risk ≥5%, 435 (3.8%) developed AF before age 65 years, with roughly half (46.9%) meeting anticoagulation criteria.

conclusionsAF risk estimation using clinical factors may prioritize individuals for AF screening more precisely than the age threshold endorsed in current guidelines. The additional value of genetic predisposition is modest but greatest among younger individuals.

Indexed as

Atrial FibrillationModels, CardiovascularModels, GeneticAge FactorsFemaleHumansMaleMiddle AgedRisk Factorsagingatrial fibrillationgenetic predisposition to diseasegenomicsrisk assessment

Identifiers

PMID34463125
PMCPMC8530935
OpenAlexW3197999035

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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.