Exposure to volatile organic compounds – acrolein, 1,3-butadiene, and crotonaldehyde – is associated with vascular dysfunction

Cardiovascular disease (CVD) is the leading cause of mortality worldwide. Exposure to air pollution, specifically particulate matter of diameter ≤2.5 μm (PM2.5), is a well-established risk factor for CVD. However, the contribution of gaseous pollutant exposure to CVD risk is less clear. To examine t...

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Bibliographic Details
Published inEnvironmental research Vol. 196; p. 110903
Main Authors McGraw, Katlyn E., Riggs, Daniel W., Rai, Shesh, Navas-Acien, Ana, Xie, Zhengzhi, Lorkiewicz, Pawel, Lynch, Jordan, Zafar, Nagma, Krishnasamy, Sathya, Taylor, Kira C., Conklin, Daniel J., DeFilippis, Andrew P., Srivastava, Sanjay, Bhatnagar, Aruni
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Inc 01.05.2021
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Summary:Cardiovascular disease (CVD) is the leading cause of mortality worldwide. Exposure to air pollution, specifically particulate matter of diameter ≤2.5 μm (PM2.5), is a well-established risk factor for CVD. However, the contribution of gaseous pollutant exposure to CVD risk is less clear. To examine the vascular effects of exposure to individual volatile organic compounds (VOCs) and mixtures of VOCs. We measured urinary metabolites of acrolein (CEMA and 3HPMA), 1,3-butadiene (DHBMA and MHBMA3), and crotonaldehyde (HPMMA) in 346 nonsmokers with varying levels of CVD risk. On the day of enrollment, we measured blood pressure (BP), reactive hyperemia index (RHI – a measure of endothelial function), and urinary levels of catecholamines and their metabolites. We used generalized linear models for evaluating the association between individual VOC metabolites and BP, RHI, and catecholamines, and we used Bayesian Kernel Machine Regression (BKMR) to assess exposure to VOC metabolite mixtures and BP. We found that the levels of 3HPMA were positively associated with systolic BP (0.98 mmHg per interquartile range (IQR) of 3HPMA; CI: 0.06, 1.91; P = 0.04). Stratified analysis revealed an increased association with systolic BP in Black participants despite lower levels of urinary 3HPMA. This association was independent of PM2.5 exposure and BP medications. BKMR analysis confirmed that 3HPMA was the major metabolite associated with higher BP in the presence of other metabolites. We also found that 3HPMA and DHBMA were associated with decreased endothelial function. For each IQR of 3HPMA or DHBMA, there was a −4.4% (CI: −7.2, −0.0; P = 0.03) and a −3.9% (CI: −9.4, −0.0; P = 0.04) difference in RHI, respectively. Although in the entire cohort the levels of several urinary VOC metabolites were weakly associated with urinary catecholamines and their metabolites, in Black participants, DHBMA levels showed strong associations with urinary norepinephrine and normetanephrine levels. Exposure to acrolein and 1,3-butadiene is associated with endothelial dysfunction and may contribute to elevated risk of hypertension in participants with increased sympathetic tone, particularly in Black individuals. •Volatile organic compounds (VOCs) are major components of environmental pollution.•Exposure to VOCs is associated with high blood pressure and endothelial dysfunction.•Exposure to VOCs is also associated with increased levels of catecholamines.•Black participants were more susceptible to vascular changes in response to exposure.•Exposure to VOCs may be a significant risk factor in the development of heart disease.
Bibliography:Shesh Rai-biostatistician, analysis guidance, reviewed and edited
Daniel J. Conklin-study design, data collection and patient recruitment, reviewed and edited
Ana Navas-Acien- BKMR and mixture analysis guidance, reviewed and edited
Andrew P. DeFilippis-study design, data collection and patient recruitment, reviewed and edited
Kira C. Taylor-epidemiology, clinical relevance, guidance, reviewed and edited
Sanjay Srivastava-study design, reviewed and edited, guiding mentor
Jordan Lynch-patient recruitment, data collection, reviewed and edited
AUTHOR CONTRIBUTIONS
Pawel Lorkiewicz- volatile organic compound and catecholamine quantification method production and GC analysis, reviewed and edited
Daniel W. Riggs-biostatistician, analysis guidance, reviewed and edited
Zhengzhi Xie- volatile organic compound and catecholamine GC analysis, reviewed and edited
Aruni Bhatnagar-study design, corresponding author, editor, guiding mentor
Sathya Krishnasamy-lab analyst, reviewed
Nagma Zafar-patient recruitment, data collection, reviewed and edited
Katlyn E. McGraw-primary author and analyst; author conducted all analyses, designed figures and tables, and wrote all text
ISSN:0013-9351
1096-0953
DOI:10.1016/j.envres.2021.110903