Short time exposure to ambient ozone and associated cardiovascular effects: A panel study of healthy young adults

被引:30
作者
Song, Jie [1 ]
Zhu, Jingfang [1 ]
Tian, Ge [1 ]
Li, Haibin [1 ]
Li, Huijun [1 ]
An, Zhen [1 ]
Jiang, Jing [1 ]
Fan, Wei [1 ]
Wang, Gui [1 ]
Zhang, Yange [1 ]
Wu, Weidong [1 ]
机构
[1] Xinxiang Med Univ, Sch Publ Hlth, Henan Int Collaborat Lab Hlth Effects & Intervent, Xinxiang 453003, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Ozone; Blood pressure; Systemic biomarker; Glutathione S-Transferase; PARTICULATE AIR-POLLUTION; SHORT-TERM EXPOSURE; BLOOD-PRESSURE; OXIDATIVE STRESS; DAILY MORTALITY; DISEASE; INFLAMMATION; TEMPERATURE; MATTER; AGGREGATION;
D O I
10.1016/j.envint.2020.105579
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The evidence that exposure to ambient ozone (O-3) causes acute cardiovascular effects appears inconsistent. A repeated-measure study with 61 healthy young volunteers was conducted in Xinxiang, Central China. Real-time concentrations of O-3 were monitored. Cardiovascular outcomes including blood pressure (BP), heart rate (HR), serum levels of high sensitivity C-reactive protein (hs-CRP), 8-hydroxy-2'-deoxyguanosine (8-OHdG), tissue-type plasminogen activator (t-PA), and platelet-monocyte aggregation (PMA) were repeated measured. Linear mixed-effect models were used to analyze the association of ambient O-3 with these cardiovascular outcomes. Additionally, the modifying effects of glutathione S-transferase mu 1 (GSTM1) and glutathione S-transferase theta 1 (GSTT1) polymorphisms were estimated to explore the potential mechanisms and role of the association between O-3 exposure and the above cardiovascular outcomes. A 10 mu g/m(3) increase in O-3 was associated with increases of 9.2 mmHg (95% confidence interval [CI]: 2.5, 15.9), 7.2 mmHg (95% CI: 0.8, 13.6), and 21.2 bpm (95% CI: 5.8, 36.6) in diastolic BP (DBP, lag1), mean arterial BP (MABP, lag1), and HR (lag01), respectively. Meanwhile, the serum concentrations of hs-CRP, 8-OHdG, and t-PA were all increased by O-3 exposure, but the PMA level was decreased. Stratification analyses showed that the estimated effects of O-3 on DBP, MABP, and HR in GSTM1-sufficient subjects were significantly higher than in GSTM1-null subjects. Moreover, GSTM1-null genotype enhanced O-3-induced increases, albeit insignificant, in levels of serum hs-CRP, 8-OHdG, and t-PA compared with GSTM1-sufficient genotype. Insignificant increases in hs-CRP and t-PA were also detected in GSTT1-null subjects. Taken together, our findings indicate that acute exposure to ambient O-3 induces autonomic alterations, systemic inflammation, oxidative stress, and fibrinolysis in healthy young subjects. GSTM1 genotype presents the trend of modifying O-3-induced cardiovascular effects.
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页数:8
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