Evidence map›Paper›PMID 40357661›Full record

ArticleJournal of the American Heart Association2025

Cross-Ancestry Associations of Spontaneous Coronary Artery Dissection Genetic Risk With Coronary Atherosclerosis and Migraine Headache.

Chang Xu, Min-Lee Yang, Pik Fang Kho, Shoa L Clarke, Catherine Tcheandjieu, Patricia A Peyser, Cathy Shen-Jang Fann, Shih-Pin Chen, VA Million Veteran Program, Jacqueline Saw and 3 more

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Chang XuDepartment of Biostatistics and Center for Statistical Genetics University of Michigan School of Public Health Ann Arbor MI USA.ORCID 0000-0003-2831-1604
Min-Lee YangDivision of Cardiovascular Medicine, Department of Internal Medicine University of Michigan Medical School Ann Arbor MI USA.ORCID 0000-0003-2823-8320
Pik Fang KhoVA Palo Alto Health Care System Palo Alto CA USA.ORCID 0000-0001-7831-6062
Shoa L ClarkeVA Palo Alto Health Care System Palo Alto CA USA.ORCID 0000-0002-6592-1172
Catherine TcheandjieuVA Palo Alto Health Care System Palo Alto CA USA.ORCID 0000-0001-9559-4339
Patricia A PeyserDepartment of Epidemiology University of Michigan School of Public Health Ann Arbor MI USA.ORCID 0000-0002-9717-8459
Cathy Shen-Jang FannInstitute of Biomedical Sciences, Academia Sinica Taipei Taiwan.ORCID 0000-0001-9025-2276
Shih-Pin ChenDepartment of Medical Research Taipei Veterans General Hospital Taipei Taiwan.ORCID 0000-0003-3492-9902
VA Million Veteran Program
Jacqueline SawVancouver General Hospital, Division of Cardiology University of British Columbia Vancouver Canada.ORCID 0000-0002-7027-984X
Xiang ZhouDepartment of Biostatistics and Center for Statistical Genetics University of Michigan School of Public Health Ann Arbor MI USA.ORCID 0000-0002-4331-7599
Themistocles L AssimesVA Palo Alto Health Care System Palo Alto CA USA.ORCID 0000-0003-2349-0009
Santhi K GaneshDivision of Cardiovascular Medicine, Department of Internal Medicine University of Michigan Medical School Ann Arbor MI USA.ORCID 0000-0002-3663-5249

Funding

Genome-Wide Association Analysis in Essential Hypertension (FEHGAS study)R01HL086694 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ARAVINDA CHAKRAVARTI · 2007 to 2026
$21.2M
Genomic and Functional Studies of Dysplasia-Associated Arterial DiseasesR35HL161016 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SANTHI K GANESH · 2022 to 2026
$4.6M
Genetic Studies of The Impact of Hematologic Traits On Cardiovascular DiseaseR01HL122684 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GANESH, SANTHI K · 2015 to 2019
$3.4M
New methods for constructing and evaluating polygenic scoresR01HG011432 · NHGRI · STANFORD UNIVERSITY · PI PRITCHARD, JONATHAN K · 2020 to 2023
$3.3M
Statistical Methods for Modeling Polygenic Architecture in Association and Re-sequencing StudiesR01HG009124 · NHGRI · YALE UNIVERSITY · PI Xiang Zhou · 2017 to 2026
$3.0M
Genetic and Genomic Analysis of Arterial DysplasiaR01HL139672 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GANESH, SANTHI K · 2018 to 2021
$2.9M
BLRD VA I01 BX003362NHGRI NIH HHS R01 HG009124NHGRI NIH HHS R01 HG011432NHLBI NIH HHS R01 HL086694NHLBI NIH HHS R01 HL122684NHLBI NIH HHS R01 HL139672NHLBI NIH HHS R35 HL161016
6 · The paper itself

Abstract

backgroundResearch studies of spontaneous coronary artery dissection (SCAD) have been primarily focused on European-ancestry individuals, with limited recognition and investigation in non-European-ancestry individuals. While SCAD has not been well ascertained in non-European-ancestry groups, pleiotropic associated traits identified in those of European ancestry have been assessed in individuals of other ancestries. Whether these traits are associated with the complex genetic architecture of SCAD in those of non-European ancestry has not been previously investigated.

methodsWe investigated the associations of an established SCAD polygenic score with multiple vascular diseases in ≈900 000 ancestrally diverse participants of large-scale studies. Individual-level data from the UK Biobank and the Million Veteran Program and summary statistics of publicly available databases were analyzed.

resultsA set of associations between SCAD polygenic score and related vascular diseases were replicated in non-European samples. Notable associations with the SCAD polygenic score included (1) coronary artery disease, myocardial infarction, and migraine headache in a Hispanic group (coronary artery disease: odds ratio [OR], 0.93 [95% CI, 0.90-0.95];

conclusionsPleiotropic associations of SCAD polygenic risk with related vascular diseases previously identified in European-ancestry groups showed notable, largely consistent patterns in non-European-ancestry groups.

Indexed as

Coronary Artery DiseaseCoronary Vessel AnomaliesMigraine DisordersPopulation GroupsVascular DiseasesAdultAgedFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedMultifactorial InheritanceMyocardial InfarctionPhenotypeRisk Assessmentdiversitygeneticspolygenic scoresspontaneous coronary artery dissectionvascular diseases

Identifiers

PMID40357661
PMCPMC12184546

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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.