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Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants
Arterial stiffness index (ASI) is a non-invasive measure of arterial stiffness using infra-red finger sensors (photoplethysmography). It is a well-suited measure for large populations as it is relatively inexpensive to perform, and data can be acquired within seconds. These features raise interest i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591384/ https://www.ncbi.nlm.nih.gov/pubmed/31235810 http://dx.doi.org/10.1038/s41598-019-45703-0 |
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author | Fung, Kenneth Ramírez, Julia Warren, Helen R. Aung, Nay Lee, Aaron M. Tzanis, Evan Petersen, Steffen E. Munroe, Patricia B. |
author_facet | Fung, Kenneth Ramírez, Julia Warren, Helen R. Aung, Nay Lee, Aaron M. Tzanis, Evan Petersen, Steffen E. Munroe, Patricia B. |
author_sort | Fung, Kenneth |
collection | PubMed |
description | Arterial stiffness index (ASI) is a non-invasive measure of arterial stiffness using infra-red finger sensors (photoplethysmography). It is a well-suited measure for large populations as it is relatively inexpensive to perform, and data can be acquired within seconds. These features raise interest in using ASI as a tool to estimate cardiovascular disease risk as prior work demonstrates increased arterial stiffness is associated with elevated systolic blood pressure, and ASI is predictive of cardiovascular disease and mortality. We conducted genome-wide association studies (GWASs) for ASI in 127,121 UK Biobank participants of European-ancestry. Our primary analyses identified variants at four loci reaching genome-wide significance (P < 5 × 10(−8)): TEX41 (rs1006923; P = 5.3 × 10(−12)), FOXO1 (rs7331212; P = 2.2 × 10(−11)), C1orf21 (rs1930290, P = 1.1 × 10(−8)) and MRVI1 (rs10840457, P = 3.4 × 10(−8)). Gene-based testing revealed three significant genes, the most significant gene was COL4A2 (P = 1.41 × 10(−8)) encoding type IV collagen. Other candidate genes at associated loci were also involved in smooth muscle tone regulation. Our findings provide new information for understanding the development of arterial stiffness. |
format | Online Article Text |
id | pubmed-6591384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65913842019-07-02 Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants Fung, Kenneth Ramírez, Julia Warren, Helen R. Aung, Nay Lee, Aaron M. Tzanis, Evan Petersen, Steffen E. Munroe, Patricia B. Sci Rep Article Arterial stiffness index (ASI) is a non-invasive measure of arterial stiffness using infra-red finger sensors (photoplethysmography). It is a well-suited measure for large populations as it is relatively inexpensive to perform, and data can be acquired within seconds. These features raise interest in using ASI as a tool to estimate cardiovascular disease risk as prior work demonstrates increased arterial stiffness is associated with elevated systolic blood pressure, and ASI is predictive of cardiovascular disease and mortality. We conducted genome-wide association studies (GWASs) for ASI in 127,121 UK Biobank participants of European-ancestry. Our primary analyses identified variants at four loci reaching genome-wide significance (P < 5 × 10(−8)): TEX41 (rs1006923; P = 5.3 × 10(−12)), FOXO1 (rs7331212; P = 2.2 × 10(−11)), C1orf21 (rs1930290, P = 1.1 × 10(−8)) and MRVI1 (rs10840457, P = 3.4 × 10(−8)). Gene-based testing revealed three significant genes, the most significant gene was COL4A2 (P = 1.41 × 10(−8)) encoding type IV collagen. Other candidate genes at associated loci were also involved in smooth muscle tone regulation. Our findings provide new information for understanding the development of arterial stiffness. Nature Publishing Group UK 2019-06-24 /pmc/articles/PMC6591384/ /pubmed/31235810 http://dx.doi.org/10.1038/s41598-019-45703-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Fung, Kenneth Ramírez, Julia Warren, Helen R. Aung, Nay Lee, Aaron M. Tzanis, Evan Petersen, Steffen E. Munroe, Patricia B. Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants |
title | Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants |
title_full | Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants |
title_fullStr | Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants |
title_full_unstemmed | Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants |
title_short | Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants |
title_sort | genome-wide association study identifies loci for arterial stiffness index in 127,121 uk biobank participants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591384/ https://www.ncbi.nlm.nih.gov/pubmed/31235810 http://dx.doi.org/10.1038/s41598-019-45703-0 |
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