Christina Lee Brown Envirome Institute, 302 E Muhammad Ali Blvd, Louisville, KY, 40202, USA; Superfund Research Center, 302 E Muhammad Ali Blvd, Louisville, KY 40202, USA; University of Louisville School of Public Health and Information Sciences, USA; Department of Environmental and Occupational Health Sciences, USA.
Christina Lee Brown Envirome Institute, 302 E Muhammad Ali Blvd, Louisville, KY, 40202, USA; Superfund Research Center, 302 E Muhammad Ali Blvd, Louisville, KY 40202, USA; University of Louisville School of Public Health and Information Sciences, USA; Department of Epidemiology and Population Health, USA.
Environ Res. 2021 May;196:110903. doi: 10.1016/j.envres.2021.110903. Epub 2021 Feb 24.
Cardiovascular disease (CVD) is the leading cause of mortality worldwide. Exposure to air pollution, specifically particulate matter of diameter ≤2.5 μm (PM), 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 PM 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.
心血管疾病(CVD)是全球范围内导致死亡的主要原因。暴露于空气污染,特别是直径≤2.5μm 的颗粒物(PM),是 CVD 的一个已确立的危险因素。然而,气态污染物暴露对 CVD 风险的贡献尚不清楚。
研究暴露于个别挥发性有机化合物(VOC)和 VOC 混合物对血管的影响。
我们在 346 名不同 CVD 风险水平的不吸烟者中测量了丙烯醛(CEMA 和 3HPMA)、1,3-丁二烯(DHBMA 和 MHBMA3)和丙烯醛(HPMMA)的尿代谢产物。在入组当天,我们测量了血压(BP)、反应性充血指数(RHI-内皮功能的衡量标准)和尿儿茶酚胺及其代谢产物的水平。我们使用广义线性模型评估单个 VOC 代谢产物与 BP、RHI 和儿茶酚胺之间的关联,我们使用贝叶斯核机器回归(BKMR)评估 VOC 代谢产物混合物与 BP 的暴露情况。
我们发现,3HPMA 的水平与收缩压呈正相关(每 3HPMA 四分位距的 0.98mmHg;CI:0.06,1.91;P=0.04)。分层分析显示,尽管黑人参与者的尿 3HPMA 水平较低,但与收缩压的关联更强。这种关联独立于 PM 暴露和 BP 药物。BKMR 分析证实,在存在其他代谢物的情况下,3HPMA 是与较高 BP 相关的主要代谢物。我们还发现 3HPMA 和 DHBMA 与内皮功能下降有关。对于 3HPMA 或 DHBMA 的每一个 IQR,RHI 分别下降了-4.4%(CI:-7.2,-0.0;P=0.03)和-3.9%(CI:-9.4,-0.0;P=0.04)。尽管在整个队列中,一些尿 VOC 代谢产物的水平与尿儿茶酚胺及其代谢产物呈弱相关,但在黑人参与者中,DHBMA 水平与尿去甲肾上腺素和去甲变肾上腺素水平呈强烈相关。
丙烯醛和 1,3-丁二烯的暴露与内皮功能障碍有关,可能导致交感神经张力增加的参与者高血压风险升高,尤其是在黑人中。