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Impact of biological aging on arterial aging in American Indians: findings from the Strong Heart Family Study

Telomere length, a marker of biological aging, has been associated with cardiovascular disease (CVD). Increased arterial stiffness, an indicator of arterial aging, predicts adverse CVD outcomes. However, the relationship between telomere length and arterial stiffness is less well studied. Here we ex...

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Autores principales: Peng, Hao, Zhu, Yun, Yeh, Fawn, Cole, Shelley A., Best, Lyle G., Lin, Jue, Blackburn, Elizabeth, Devereux, Richard B., Roman, Mary J., Lee, Elisa T., Howard, Barbara V., Zhao, Jinying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5032684/
https://www.ncbi.nlm.nih.gov/pubmed/27540694
http://dx.doi.org/10.18632/aging.101013
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author Peng, Hao
Zhu, Yun
Yeh, Fawn
Cole, Shelley A.
Best, Lyle G.
Lin, Jue
Blackburn, Elizabeth
Devereux, Richard B.
Roman, Mary J.
Lee, Elisa T.
Howard, Barbara V.
Zhao, Jinying
author_facet Peng, Hao
Zhu, Yun
Yeh, Fawn
Cole, Shelley A.
Best, Lyle G.
Lin, Jue
Blackburn, Elizabeth
Devereux, Richard B.
Roman, Mary J.
Lee, Elisa T.
Howard, Barbara V.
Zhao, Jinying
author_sort Peng, Hao
collection PubMed
description Telomere length, a marker of biological aging, has been associated with cardiovascular disease (CVD). Increased arterial stiffness, an indicator of arterial aging, predicts adverse CVD outcomes. However, the relationship between telomere length and arterial stiffness is less well studied. Here we examined the cross-sectional association between leukocyte telomere length (LTL) and arterial stiffness in 2,165 American Indians in the Strong Heart Family Study (SHFS). LTL was measured by qPCR. Arterial stiffness was assessed by stiffness index β. The association between LTL and arterial stiffness was assessed by generalized estimating equation model, adjusting for sociodemographics (age, sex, education level), study site, metabolic factors (fasting glucose, lipids, systolic blood pressure, and kidney function), lifestyle (BMI, smoking, drinking, and physical activity), and prevalent CVD. Results showed that longer LTL was significantly associated with a decreased arterial stiffness (β=-0.070, P=0.007). This association did not attenuate after further adjustment for hsCRP (β=-0.071, P=0.005) or excluding participants with overt CVD (β=-0.068, P=0.012), diabetes (β=-0.070, P=0.005), or chronic kidney disease (β=-0.090, P=0.001). In summary, shorter LTL was significantly associated with an increased arterial stiffness, independent of known risk factors. This finding may shed light on the potential role of biological aging in arterial aging in American Indians.
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spelling pubmed-50326842016-09-29 Impact of biological aging on arterial aging in American Indians: findings from the Strong Heart Family Study Peng, Hao Zhu, Yun Yeh, Fawn Cole, Shelley A. Best, Lyle G. Lin, Jue Blackburn, Elizabeth Devereux, Richard B. Roman, Mary J. Lee, Elisa T. Howard, Barbara V. Zhao, Jinying Aging (Albany NY) Priority Research Paper Telomere length, a marker of biological aging, has been associated with cardiovascular disease (CVD). Increased arterial stiffness, an indicator of arterial aging, predicts adverse CVD outcomes. However, the relationship between telomere length and arterial stiffness is less well studied. Here we examined the cross-sectional association between leukocyte telomere length (LTL) and arterial stiffness in 2,165 American Indians in the Strong Heart Family Study (SHFS). LTL was measured by qPCR. Arterial stiffness was assessed by stiffness index β. The association between LTL and arterial stiffness was assessed by generalized estimating equation model, adjusting for sociodemographics (age, sex, education level), study site, metabolic factors (fasting glucose, lipids, systolic blood pressure, and kidney function), lifestyle (BMI, smoking, drinking, and physical activity), and prevalent CVD. Results showed that longer LTL was significantly associated with a decreased arterial stiffness (β=-0.070, P=0.007). This association did not attenuate after further adjustment for hsCRP (β=-0.071, P=0.005) or excluding participants with overt CVD (β=-0.068, P=0.012), diabetes (β=-0.070, P=0.005), or chronic kidney disease (β=-0.090, P=0.001). In summary, shorter LTL was significantly associated with an increased arterial stiffness, independent of known risk factors. This finding may shed light on the potential role of biological aging in arterial aging in American Indians. Impact Journals LLC 2016-08-11 /pmc/articles/PMC5032684/ /pubmed/27540694 http://dx.doi.org/10.18632/aging.101013 Text en Copyright: © 2016 Peng et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Priority Research Paper
Peng, Hao
Zhu, Yun
Yeh, Fawn
Cole, Shelley A.
Best, Lyle G.
Lin, Jue
Blackburn, Elizabeth
Devereux, Richard B.
Roman, Mary J.
Lee, Elisa T.
Howard, Barbara V.
Zhao, Jinying
Impact of biological aging on arterial aging in American Indians: findings from the Strong Heart Family Study
title Impact of biological aging on arterial aging in American Indians: findings from the Strong Heart Family Study
title_full Impact of biological aging on arterial aging in American Indians: findings from the Strong Heart Family Study
title_fullStr Impact of biological aging on arterial aging in American Indians: findings from the Strong Heart Family Study
title_full_unstemmed Impact of biological aging on arterial aging in American Indians: findings from the Strong Heart Family Study
title_short Impact of biological aging on arterial aging in American Indians: findings from the Strong Heart Family Study
title_sort impact of biological aging on arterial aging in american indians: findings from the strong heart family study
topic Priority Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5032684/
https://www.ncbi.nlm.nih.gov/pubmed/27540694
http://dx.doi.org/10.18632/aging.101013
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