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A genome-wide association study of imaging-defined atherosclerosis
Region Västra Götaland, Sahlgrenska University Hospital, Department of Clinical Genetics and Genomics, Gothenburg, Sweden; Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Medical Sciences, Molecular Epidemiology, Uppsala University, Uppsala, Sweden.
Division of Cardiology, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
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2025 (English)In: Nature Communications, E-ISSN 2041-1723, Vol. 16, no 1, article id 2266Article in journal (Refereed) Published
Abstract [en]

Imaging-defined atherosclerosis represents an intermediate phenotype of atherosclerotic cardiovascular disease (ASCVD). Genome-wide association studies (GWAS) on directly measured coronary plaques using coronary computed tomography angiography (CCTA) are scarce. In the so far largest population-based cohort with CCTA data, we performed a GWAS on coronary plaque burden as determined by the segment involvement score (SIS) in 24,811 European individuals. We identified 20 significant independent genetic markers for SIS, three of which were found in loci not implicated in ASCVD before. Further GWAS on coronary artery calcification showed similar results to that of SIS, whereas a GWAS on ultrasound-assessed carotid plaques identified both shared and non-shared loci with SIS. In two-sample Mendelian randomization studies using SIS-associated markers in UK Biobank and CARDIoGRAMplusC4D, one extra coronary segment with atherosclerosis corresponded to 1.8-fold increased odds of myocardial infarction. This GWAS data can aid future studies of causal pathways in ASCVD.

Place, publisher, year, edition, pages
Nature Publishing Group, 2025. Vol. 16, no 1, article id 2266
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Cardiology and Cardiovascular Disease Medical Genetics and Genomics
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URN: urn:nbn:se:umu:diva-237375DOI: 10.1038/s41467-025-57457-7ISI: 001456731600020PubMedID: 40164586Scopus ID: 2-s2.0-105001450683OAI: oai:DiVA.org:umu-237375DiVA, id: diva2:1953978
Funder
Swedish Heart Lung Foundation, 2023-0439Swedish Heart Lung Foundation, 2024-1135Swedish Heart Lung Foundation, 2024-1137Swedish Research Council, 2023-02177Available from: 2025-04-23 Created: 2025-04-23 Last updated: 2025-04-23Bibliographically approved

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