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Cardiac Autonomic Dysfunction: Particulate Air Pollution Effects Are Modulated by Epigenetic Immunoregulation of Toll‐like Receptor 2 and Dietary Flavonoid Intake

BACKGROUND: Short‐term fine particles (PM(2.5)) exposure is associated with reduced heart rate variability, a strong predictor of cardiac mortality among older people. Identifying modifiable factors that confer susceptibility is essential for intervention. We evaluated whether Toll‐like receptor 2 (...

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Autores principales: Zhong, Jia, Colicino, Elena, Lin, Xinyi, Mehta, Amar, Kloog, Itai, Zanobetti, Antonella, Byun, Hyang‐Min, Bind, Marie‐Abèle, Cantone, Laura, Prada, Diddier, Tarantini, Letizia, Trevisi, Letizia, Sparrow, David, Vokonas, Pantel, Schwartz, Joel, Baccarelli, Andrea A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330067/
https://www.ncbi.nlm.nih.gov/pubmed/25628407
http://dx.doi.org/10.1161/JAHA.114.001423
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author Zhong, Jia
Colicino, Elena
Lin, Xinyi
Mehta, Amar
Kloog, Itai
Zanobetti, Antonella
Byun, Hyang‐Min
Bind, Marie‐Abèle
Cantone, Laura
Prada, Diddier
Tarantini, Letizia
Trevisi, Letizia
Sparrow, David
Vokonas, Pantel
Schwartz, Joel
Baccarelli, Andrea A.
author_facet Zhong, Jia
Colicino, Elena
Lin, Xinyi
Mehta, Amar
Kloog, Itai
Zanobetti, Antonella
Byun, Hyang‐Min
Bind, Marie‐Abèle
Cantone, Laura
Prada, Diddier
Tarantini, Letizia
Trevisi, Letizia
Sparrow, David
Vokonas, Pantel
Schwartz, Joel
Baccarelli, Andrea A.
author_sort Zhong, Jia
collection PubMed
description BACKGROUND: Short‐term fine particles (PM(2.5)) exposure is associated with reduced heart rate variability, a strong predictor of cardiac mortality among older people. Identifying modifiable factors that confer susceptibility is essential for intervention. We evaluated whether Toll‐like receptor 2 (TLR2) methylation, a reversible immune‐epigenetic process, and its dietary modulation by flavonoids and methyl nutrients, modify susceptibility to heart rate variability effects following PM(2.5) exposure. METHODS AND RESULTS: We measured heart rate variability and PM(2.5) repeatedly over 11 years (1275 total observations) among 573 elderly men from the Normative Aging Study. Blood TLR2 methylation was analyzed using pyrosequencing. Daily flavonoid and methyl nutrients intakes were assessed through the Food Frequency Questionnaire (FFQ). Every 10 μg/m(3) increase in 48‐hour PM(2.5) moving average was associated with 7.74% (95% CI: −1.21% to 15.90%; P=0.09), 7.46% (95% CI: 0.99% to 13.50%; P=0.02), 14.18% (95% CI: 1.14% to 25.49%; P=0.03), and 12.94% (95% CI: −2.36% to 25.96%; P=0.09) reductions in root mean square of successive differences, standard deviation of normal‐to‐normal intervals, low‐frequency power, and high‐frequency power, respectively. Higher TLR2 methylation exacerbated the root mean square of successive differences, standard deviation of normal‐to‐normal intervals, low‐frequency, and high‐frequency reductions associated with heightened PM(2.5) (P(interaction)=0.006, 0.03, 0.05, 0.04, respectively). Every interquartile‐range increase in flavonoid intake was associated with 5.09% reduction in mean TLR2 methylation (95% CI: 0.12% to 10.06%; P=0.05) and counteracted the effects of PM(2.5) on low frequency (P(interaction)=0.05). No significant effect of methyl nutrients on TLR2 methylation was observed. CONCLUSIONS: Higher TLR2 methylation may confer susceptibility to adverse cardiac autonomic effects of PM(2.5) exposure in older individuals. Higher flavonoid intake may attenuate these effects, possibly by decreasing TLR2 methylation.
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spelling pubmed-43300672015-02-27 Cardiac Autonomic Dysfunction: Particulate Air Pollution Effects Are Modulated by Epigenetic Immunoregulation of Toll‐like Receptor 2 and Dietary Flavonoid Intake Zhong, Jia Colicino, Elena Lin, Xinyi Mehta, Amar Kloog, Itai Zanobetti, Antonella Byun, Hyang‐Min Bind, Marie‐Abèle Cantone, Laura Prada, Diddier Tarantini, Letizia Trevisi, Letizia Sparrow, David Vokonas, Pantel Schwartz, Joel Baccarelli, Andrea A. J Am Heart Assoc Original Research BACKGROUND: Short‐term fine particles (PM(2.5)) exposure is associated with reduced heart rate variability, a strong predictor of cardiac mortality among older people. Identifying modifiable factors that confer susceptibility is essential for intervention. We evaluated whether Toll‐like receptor 2 (TLR2) methylation, a reversible immune‐epigenetic process, and its dietary modulation by flavonoids and methyl nutrients, modify susceptibility to heart rate variability effects following PM(2.5) exposure. METHODS AND RESULTS: We measured heart rate variability and PM(2.5) repeatedly over 11 years (1275 total observations) among 573 elderly men from the Normative Aging Study. Blood TLR2 methylation was analyzed using pyrosequencing. Daily flavonoid and methyl nutrients intakes were assessed through the Food Frequency Questionnaire (FFQ). Every 10 μg/m(3) increase in 48‐hour PM(2.5) moving average was associated with 7.74% (95% CI: −1.21% to 15.90%; P=0.09), 7.46% (95% CI: 0.99% to 13.50%; P=0.02), 14.18% (95% CI: 1.14% to 25.49%; P=0.03), and 12.94% (95% CI: −2.36% to 25.96%; P=0.09) reductions in root mean square of successive differences, standard deviation of normal‐to‐normal intervals, low‐frequency power, and high‐frequency power, respectively. Higher TLR2 methylation exacerbated the root mean square of successive differences, standard deviation of normal‐to‐normal intervals, low‐frequency, and high‐frequency reductions associated with heightened PM(2.5) (P(interaction)=0.006, 0.03, 0.05, 0.04, respectively). Every interquartile‐range increase in flavonoid intake was associated with 5.09% reduction in mean TLR2 methylation (95% CI: 0.12% to 10.06%; P=0.05) and counteracted the effects of PM(2.5) on low frequency (P(interaction)=0.05). No significant effect of methyl nutrients on TLR2 methylation was observed. CONCLUSIONS: Higher TLR2 methylation may confer susceptibility to adverse cardiac autonomic effects of PM(2.5) exposure in older individuals. Higher flavonoid intake may attenuate these effects, possibly by decreasing TLR2 methylation. Blackwell Publishing Ltd 2015-01-27 /pmc/articles/PMC4330067/ /pubmed/25628407 http://dx.doi.org/10.1161/JAHA.114.001423 Text en © 2015 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research
Zhong, Jia
Colicino, Elena
Lin, Xinyi
Mehta, Amar
Kloog, Itai
Zanobetti, Antonella
Byun, Hyang‐Min
Bind, Marie‐Abèle
Cantone, Laura
Prada, Diddier
Tarantini, Letizia
Trevisi, Letizia
Sparrow, David
Vokonas, Pantel
Schwartz, Joel
Baccarelli, Andrea A.
Cardiac Autonomic Dysfunction: Particulate Air Pollution Effects Are Modulated by Epigenetic Immunoregulation of Toll‐like Receptor 2 and Dietary Flavonoid Intake
title Cardiac Autonomic Dysfunction: Particulate Air Pollution Effects Are Modulated by Epigenetic Immunoregulation of Toll‐like Receptor 2 and Dietary Flavonoid Intake
title_full Cardiac Autonomic Dysfunction: Particulate Air Pollution Effects Are Modulated by Epigenetic Immunoregulation of Toll‐like Receptor 2 and Dietary Flavonoid Intake
title_fullStr Cardiac Autonomic Dysfunction: Particulate Air Pollution Effects Are Modulated by Epigenetic Immunoregulation of Toll‐like Receptor 2 and Dietary Flavonoid Intake
title_full_unstemmed Cardiac Autonomic Dysfunction: Particulate Air Pollution Effects Are Modulated by Epigenetic Immunoregulation of Toll‐like Receptor 2 and Dietary Flavonoid Intake
title_short Cardiac Autonomic Dysfunction: Particulate Air Pollution Effects Are Modulated by Epigenetic Immunoregulation of Toll‐like Receptor 2 and Dietary Flavonoid Intake
title_sort cardiac autonomic dysfunction: particulate air pollution effects are modulated by epigenetic immunoregulation of toll‐like receptor 2 and dietary flavonoid intake
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330067/
https://www.ncbi.nlm.nih.gov/pubmed/25628407
http://dx.doi.org/10.1161/JAHA.114.001423
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