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Retinal microcirculation and leukocyte telomere length in the general population
Retinal arteriolar narrowing increases with age and predict adverse cardiovascular outcomes. Telomere length keeps track of the division of somatic cells and is a biomarker of biological age. We investigated to what extent retinal arteriolar diameters are associated with biological age, as captured...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5935741/ https://www.ncbi.nlm.nih.gov/pubmed/29728662 http://dx.doi.org/10.1038/s41598-018-25165-6 |
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author | Martens, Dries S. Wei, Fang-Fei Cox, Bianca Plusquin, Michelle Thijs, Lutgarde Winckelmans, Ellen Zhang, Zhen-Yu Nawrot, Tim S. Staessen, Jan A. |
author_facet | Martens, Dries S. Wei, Fang-Fei Cox, Bianca Plusquin, Michelle Thijs, Lutgarde Winckelmans, Ellen Zhang, Zhen-Yu Nawrot, Tim S. Staessen, Jan A. |
author_sort | Martens, Dries S. |
collection | PubMed |
description | Retinal arteriolar narrowing increases with age and predict adverse cardiovascular outcomes. Telomere length keeps track of the division of somatic cells and is a biomarker of biological age. We investigated to what extent retinal arteriolar diameters are associated with biological age, as captured by leukocyte telomere length (LTL). In 168 randomly selected Flemish participants from the family-based population study FLEMENGHO (mean age, 46.2 years) at baseline, of whom 85 underwent a follow-up examination (median, 4.1 years), we post-processed nonmydriatic retinal photographs and measured LTL. In men only, central retinal arteriolar equivalents (CRAE) and arteriole-to-venule ratio (AVR) were associated with LTL with stronger associations at higher age and body mass index. In men aged 57.6 years (75th percentile) a 20% shorter LTL was associated with a decrease in CRAE of 4.57 µm. A 20% shorter LTL was associated with a decrease of 5.88 µm in CRAE at a BMI of 29.9 kg/m(2) (75th percentile). Similar associations were observed between AVR and LTL. In women, no retinal microvascular traits were associated with LTL. Retinal arteriolar narrowing in men but not in women is associated with biological age. Our findings support the idea that avoiding overweight contributes to maintaining a healthier microcirculation. |
format | Online Article Text |
id | pubmed-5935741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59357412018-05-10 Retinal microcirculation and leukocyte telomere length in the general population Martens, Dries S. Wei, Fang-Fei Cox, Bianca Plusquin, Michelle Thijs, Lutgarde Winckelmans, Ellen Zhang, Zhen-Yu Nawrot, Tim S. Staessen, Jan A. Sci Rep Article Retinal arteriolar narrowing increases with age and predict adverse cardiovascular outcomes. Telomere length keeps track of the division of somatic cells and is a biomarker of biological age. We investigated to what extent retinal arteriolar diameters are associated with biological age, as captured by leukocyte telomere length (LTL). In 168 randomly selected Flemish participants from the family-based population study FLEMENGHO (mean age, 46.2 years) at baseline, of whom 85 underwent a follow-up examination (median, 4.1 years), we post-processed nonmydriatic retinal photographs and measured LTL. In men only, central retinal arteriolar equivalents (CRAE) and arteriole-to-venule ratio (AVR) were associated with LTL with stronger associations at higher age and body mass index. In men aged 57.6 years (75th percentile) a 20% shorter LTL was associated with a decrease in CRAE of 4.57 µm. A 20% shorter LTL was associated with a decrease of 5.88 µm in CRAE at a BMI of 29.9 kg/m(2) (75th percentile). Similar associations were observed between AVR and LTL. In women, no retinal microvascular traits were associated with LTL. Retinal arteriolar narrowing in men but not in women is associated with biological age. Our findings support the idea that avoiding overweight contributes to maintaining a healthier microcirculation. Nature Publishing Group UK 2018-05-04 /pmc/articles/PMC5935741/ /pubmed/29728662 http://dx.doi.org/10.1038/s41598-018-25165-6 Text en © The Author(s) 2018 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 Martens, Dries S. Wei, Fang-Fei Cox, Bianca Plusquin, Michelle Thijs, Lutgarde Winckelmans, Ellen Zhang, Zhen-Yu Nawrot, Tim S. Staessen, Jan A. Retinal microcirculation and leukocyte telomere length in the general population |
title | Retinal microcirculation and leukocyte telomere length in the general population |
title_full | Retinal microcirculation and leukocyte telomere length in the general population |
title_fullStr | Retinal microcirculation and leukocyte telomere length in the general population |
title_full_unstemmed | Retinal microcirculation and leukocyte telomere length in the general population |
title_short | Retinal microcirculation and leukocyte telomere length in the general population |
title_sort | retinal microcirculation and leukocyte telomere length in the general population |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5935741/ https://www.ncbi.nlm.nih.gov/pubmed/29728662 http://dx.doi.org/10.1038/s41598-018-25165-6 |
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