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

Author:

Zhong Jia1,Colicino Elena1,Lin Xinyi23,Mehta Amar1,Kloog Itai4,Zanobetti Antonella1,Byun Hyang‐Min1,Bind Marie‐Abèle12,Cantone Laura5,Prada Diddier1,Tarantini Letizia5,Trevisi Letizia1,Sparrow David6,Vokonas Pantel6,Schwartz Joel1,Baccarelli Andrea A.1

Affiliation:

1. Department of Environmental Health, Harvard School of Public Health, Boston, MA

2. Department of Biostatistics, Harvard School of Public Health, Boston, MA

3. Singapore Institute for Clinical Sciences, Singapore

4. Department of Geography and Environmental Development, Ben‐Gurion University of the Negev, Beer Sheva, Israel

5. Center of Molecular and Genetic Epidemiology, Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milan, Italy

6. VA Normative Aging Study, Veterans Affairs Boston Healthcare System and the Department of Medicine, Boston University School of Medicine, Boston, MA

Abstract

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 ( TLR 2 ) 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 TLR 2 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 TLR 2 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 TLR 2 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 TLR 2 methylation was observed. Conclusions Higher TLR 2 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 TLR 2 methylation.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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