Evidence map›Paper›PMID 40313769›Full record

ArticleResearch square2025

A multi-trait genome-wide association study of coronary artery disease and subclinical atherosclerosis traits.

Paul de Vries, Natalie Hasbani, Adam Heath, Chani Hodonsky, Julie Hahn, Devendra Meena, Haojie Lu, Abbas Abbas Dehghan, Maryam Kavousi, Benjamin Voight and 5 more

Abstract readPreprint
In one paragraph

Article in Research square, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Paul de VriesHuman Genetics Center.ORCID 0000-0003-0964-0111
Natalie HasbaniThe University of Texas Health Science Center at Houston.ORCID 0000-0001-9874-3440
Adam HeathThe University of Texas Health Science Center at Houston.ORCID 0000-0002-5909-9055
Chani HodonskyUniversity of Virginia.
Julie HahnThe University of Texas Health Science Center at Houston.
Devendra MeenaImperial College London.
Haojie LuErasmus University Medical Center.
Abbas Abbas DehghanImperial College London.
Maryam KavousiErasmus MC.ORCID 0000-0001-5976-6519
Benjamin VoightUniversity of Pennsylvania.ORCID 0000-0002-6205-9994
Patricia PeyserDepartment of Epidemiology, School of Public Health, University of Michigan.ORCID 0000-0002-9717-8459
Alanna MorrisonThe University of Texas Health Science Center at Houston.ORCID 0000-0001-6381-4296
Themistocles AssimesStanford University School of Medicine.ORCID 0000-0003-2349-0009
Scott DamrauerUniversity of Pennsylvania.ORCID 0000-0001-8009-1632
Clint MillerUniversity of Virginia.ORCID 0000-0003-4276-3607

Funding

Multimodal genetic regulatory architecture of coronary artery diseaseR01HL148239 · NHLBI · UNIVERSITY OF VIRGINIA · PI Clint L Miller · 2019 to 2026
$4.2M
Whole-genome sequencing analysis of coronary atherosclerosis and related traitsR01HL146860 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI DE VRIES, PAUL STEFAN · 2020 to 2024
$3.9M
Molecular Drivers of Atherosclerosis in DiabetesU01DK142283 · NIDDK · UNIVERSITY OF VIRGINIA · PI Mete Civelek, Clint L Miller · 2024 to 2026
$2.9M
Functional genomics investigation of pleiotropic vascular disease lociR01HL164577 · NHLBI · UNIVERSITY OF VIRGINIA · PI MILLER, CLINT L · 2022 to 2025
$2.3M
NHLBI NIH HHS R01 HL146860NHLBI NIH HHS R01 HL148239NHLBI NIH HHS R01 HL164577NIDDK NIH HHS U01 DK142283
6 · The paper itself

Abstract

Measures of subclinical atherosclerosis, such as coronary artery calcification (CAC) and carotid intima-media thickness (CIMT), reflect the underlying pathophysiology of coronary artery disease (CAD) and are genetically correlated with CAD and related risk factors. Leveraging summary statistics from genome-wide association studies of CAD, CIMT, CAC, type 2 diabetes, low-density lipoprotein cholesterol, and systolic blood pressure, we performed 15 separate multi-trait GWAS to identify shared susceptibility loci and elucidate the pleiotropic architecture underlying atherosclerosis. We identified 442 shared risk loci across all analyses that met an experiment-wide Bonferroni threshold of 3.3 × 10

Identifiers

PMID40313769
PMCPMC12045367

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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.