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Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals

Carotid artery intima-media thickness (cIMT) is a widely accepted marker of subclinical atherosclerosis. Twenty susceptibility loci for cIMT were previously identified and the identification of additional susceptibility loci furthers our knowledge on the genetic architecture underlying atheroscleros...

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Autores principales: Yeung, Ming Wai, Wang, Siqi, van de Vegte, Yordi J., Borisov, Oleg, van Setten, Jessica, Snieder, Harold, Verweij, Niek, Said, M. Abdullah, van der Harst, Pim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8939707/
https://www.ncbi.nlm.nih.gov/pubmed/34852643
http://dx.doi.org/10.1161/ATVBAHA.121.317007
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author Yeung, Ming Wai
Wang, Siqi
van de Vegte, Yordi J.
Borisov, Oleg
van Setten, Jessica
Snieder, Harold
Verweij, Niek
Said, M. Abdullah
van der Harst, Pim
author_facet Yeung, Ming Wai
Wang, Siqi
van de Vegte, Yordi J.
Borisov, Oleg
van Setten, Jessica
Snieder, Harold
Verweij, Niek
Said, M. Abdullah
van der Harst, Pim
author_sort Yeung, Ming Wai
collection PubMed
description Carotid artery intima-media thickness (cIMT) is a widely accepted marker of subclinical atherosclerosis. Twenty susceptibility loci for cIMT were previously identified and the identification of additional susceptibility loci furthers our knowledge on the genetic architecture underlying atherosclerosis. APPROACH AND RESULTS: We performed 3 genome-wide association studies in 45 185 participants from the UK Biobank study who underwent cIMT measurements and had data on minimum, mean, and maximum thickness. We replicated 15 known loci and identified 20 novel loci associated with cIMT at P<5×10(−8). Seven novel loci (ZNF385D, ADAMTS9, EDNRA, HAND2, MYOCD, ITCH/EDEM2/MMP24, and MRTFA) were identified in all 3 phenotypes. An additional new locus (LOXL1) was identified in the meta-analysis of the 3 phenotypes. Sex interaction analysis revealed sex differences in 7 loci including a novel locus (SYNE3) in males. Meta-analysis of UK Biobank data with a previous meta-analysis led to identification of three novel loci (APOB, FIP1L1, and LOXL4). Transcriptome-wide association analyses implicated additional genes ARHGAP42, NDRG4, and KANK2. Gene set analysis showed an enrichment in extracellular organization and the PDGF (platelet-derived growth factor) signaling pathway. We found positive genetic correlations of cIMT with coronary artery disease r(g)=0.21 (P=1.4×10(-7)), peripheral artery disease r(g)=0.45 (P=5.3×10(-5)), and systolic blood pressure r(g)=0.30 (P=4.0×10(-18)). A negative genetic correlation between average of maximum cIMT and high-density lipoprotein was found r(g)=−0.12 (P=7.0×10(-4)). CONCLUSIONS: Genome-wide association meta-analyses in >100 000 individuals identified 25 novel loci associated with cIMT providing insights into genes and tissue-specific regulatory mechanisms of proatherosclerotic processes. We found evidence for shared biological mechanisms with cardiovascular diseases.
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spelling pubmed-89397072022-04-01 Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals Yeung, Ming Wai Wang, Siqi van de Vegte, Yordi J. Borisov, Oleg van Setten, Jessica Snieder, Harold Verweij, Niek Said, M. Abdullah van der Harst, Pim Arterioscler Thromb Vasc Biol Clinical and Population Studies Carotid artery intima-media thickness (cIMT) is a widely accepted marker of subclinical atherosclerosis. Twenty susceptibility loci for cIMT were previously identified and the identification of additional susceptibility loci furthers our knowledge on the genetic architecture underlying atherosclerosis. APPROACH AND RESULTS: We performed 3 genome-wide association studies in 45 185 participants from the UK Biobank study who underwent cIMT measurements and had data on minimum, mean, and maximum thickness. We replicated 15 known loci and identified 20 novel loci associated with cIMT at P<5×10(−8). Seven novel loci (ZNF385D, ADAMTS9, EDNRA, HAND2, MYOCD, ITCH/EDEM2/MMP24, and MRTFA) were identified in all 3 phenotypes. An additional new locus (LOXL1) was identified in the meta-analysis of the 3 phenotypes. Sex interaction analysis revealed sex differences in 7 loci including a novel locus (SYNE3) in males. Meta-analysis of UK Biobank data with a previous meta-analysis led to identification of three novel loci (APOB, FIP1L1, and LOXL4). Transcriptome-wide association analyses implicated additional genes ARHGAP42, NDRG4, and KANK2. Gene set analysis showed an enrichment in extracellular organization and the PDGF (platelet-derived growth factor) signaling pathway. We found positive genetic correlations of cIMT with coronary artery disease r(g)=0.21 (P=1.4×10(-7)), peripheral artery disease r(g)=0.45 (P=5.3×10(-5)), and systolic blood pressure r(g)=0.30 (P=4.0×10(-18)). A negative genetic correlation between average of maximum cIMT and high-density lipoprotein was found r(g)=−0.12 (P=7.0×10(-4)). CONCLUSIONS: Genome-wide association meta-analyses in >100 000 individuals identified 25 novel loci associated with cIMT providing insights into genes and tissue-specific regulatory mechanisms of proatherosclerotic processes. We found evidence for shared biological mechanisms with cardiovascular diseases. Lippincott Williams & Wilkins 2021-12-02 2022-04 /pmc/articles/PMC8939707/ /pubmed/34852643 http://dx.doi.org/10.1161/ATVBAHA.121.317007 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Arteriosclerosis, Thrombosis, and Vascular Biology is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited.
spellingShingle Clinical and Population Studies
Yeung, Ming Wai
Wang, Siqi
van de Vegte, Yordi J.
Borisov, Oleg
van Setten, Jessica
Snieder, Harold
Verweij, Niek
Said, M. Abdullah
van der Harst, Pim
Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals
title Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals
title_full Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals
title_fullStr Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals
title_full_unstemmed Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals
title_short Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals
title_sort twenty-five novel loci for carotid intima-media thickness: a genome-wide association study in >45 000 individuals and meta-analysis of >100 000 individuals
topic Clinical and Population Studies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8939707/
https://www.ncbi.nlm.nih.gov/pubmed/34852643
http://dx.doi.org/10.1161/ATVBAHA.121.317007
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