Evidence map›Paper›PMID 31983321›Full record

ArticleJournal of the American Heart Association2020

Genetic Risk of Coronary Artery Disease, Features of Atherosclerosis, and Coronary Plaque Burden.

Morten Krogh Christiansen, Louise Nissen, Simon Winther, Peter Loof Møller, Lars Frost, Jane Kirk Johansen, Henrik Kjærulf Jensen, Daníel Guðbjartsson, Hilma Holm, Kári Stefánsson and 3 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Journal of the American Heart Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.8field-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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
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  12. Polygenic Risk and Coronary Artery Disease Severity.Circulation. Genomic and precision medicine · 2024
    Article
  13. Article
  14. Review
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  19. Review
  20. Present and future of coronary risk assessment.European heart journal supplements : journal of the European Society of Cardiology · 2021
    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

13 authors at 5 institutions in 2 countries.

Morten Krogh ChristiansenDepartment of Cardiology Aarhus University Hospital Aarhus Denmark.
Louise NissenDepartment of Cardiology Hospital Unit West Herning Denmark.
Simon WintherDepartment of Cardiology Aarhus University Hospital Aarhus Denmark.
Peter Loof MøllerDepartment of Biomedicine Aarhus University Aarhus Denmark.
Lars FrostDepartment of Cardiology Silkeborg Regional Hospital Silkeborg Denmark.
Jane Kirk JohansenDepartment of Cardiology Silkeborg Regional Hospital Silkeborg Denmark.
Henrik Kjærulf JensenDepartment of Cardiology Aarhus University Hospital Aarhus Denmark.
Daníel GuðbjartssondeCODE Genetics/Amgen, Inc. Reykjavik Iceland.
Hilma HolmdeCODE Genetics/Amgen, Inc. Reykjavik Iceland.
Kári StefánssondeCODE Genetics/Amgen, Inc. Reykjavik Iceland.
Hans Erik BøtkerDepartment of Cardiology Aarhus University Hospital Aarhus Denmark.
Morten BøttcherDepartment of Cardiology Hospital Unit West Herning Denmark.
Mette NyegaardDepartment of Biomedicine Aarhus University Aarhus Denmark.
Aarhus University Hospital · DKdeCODE Genetics (Iceland) · ISRegional Hospital West Jutland · DKAarhus University · DKRegionshospitalet Silkeborg · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Polygenic risk scores (PRSs) based on risk variants from genome-wide association studies predict coronary artery disease (CAD) risk. However, it is unknown whether the PRS is associated with specific CAD characteristics. Methods and Results We consecutively included 1645 patients with suspected stable CAD undergoing coronary computed tomography angiography. A multilocus PRS was calculated as the weighted sum of CAD risk variants. Plaques were evaluated using an 18-segment model and characterized by stenosis severity and composition (soft [0%-19% calcified], mixed-soft [20%-49% calcified], mixed-calcified [50%-79% calcified], or calcified [≥80% calcified]). Coronary artery calcium score and segment stenosis score were used to characterize plaque burden. For each standard deviation increase in the PRS, coronary artery calcium score increased by 78% (

Indexed as

Multifactorial InheritancePlaque, AtheroscleroticComputed Tomography AngiographyCoronary AngiographyCoronary Artery DiseaseDenmarkFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHeart Disease Risk FactorsHumansMaleMiddle AgedMultidetector Computed TomographyPhenotypePrognosisatherosclerosiscoronary artery diseasecoronary computed tomography angiographyplaque

Identifiers

PMID31983321
PMCPMC7033858
OpenAlexW3001185708

What OpenQuestion holds

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LicenceCC BY-NC
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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.