Nitrated Fatty Acids and Susceptibility of COPD to Air Pollution: Evidence from a Randomized Crossover Study

IF 6.3
Yan Lin*, Ruoxue Chen, Yihui Ge, Xiaodong Liu, Kian Fan Chung and Junfeng Jim Zhang, 
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Abstract

Previous studies documented increased nitrative stress and susceptibility to air pollution among individuals with chronic inflammatory conditions. This study examines the role of anti-inflammatory and cardioprotective nitrated fatty acids (i.e., NO2-cLA) in chronic obstructive pulmonary disease (COPD)’s and ischemic heart disease (IHD)’s susceptibility to air pollution. In a randomized crossover study, 40 healthy, 40 COPD, and 39 IHD adults underwent a 2 h walk in a more polluted street or a less polluted park. We measured urinary NO2-cLA before and 24 h after the walk, as well as respiratory inflammatory biomarkers, lung function, airway resistance, and arterial stiffness. Baseline NO2-cLA levels were 2.56 (95% CI: 1.20–5.43)-fold higher among COPD participants than healthy participants, which can be explained by higher fractional exhaled nitric oxide and sputum myeloperoxidase levels. Among COPD but not healthy or IHD participants, the street walk, compared to park, led to a 57.7% (95% CI: 7.6–80.6%) decrease in NO2-cLA levels and sputum biomarker changes indicative of decreased neutrophil inflammation and proresolving responses. Decreased NO2-cLA levels were associated with exposure to black carbon and ultrafine particles and worsened lung function and arterial stiffness. Taken together, nitrated fatty acids partially mediate COPD patients’ cardiorespiratory responses to air pollution, explaining their susceptibility.

硝化脂肪酸与COPD对空气污染的易感性:来自一项随机交叉研究的证据
先前的研究表明,慢性炎症患者的硝化应激和对空气污染的易感性增加。本研究探讨了抗炎和保护心脏的硝化脂肪酸(即NO2-cLA)在慢性阻塞性肺疾病(COPD)和缺血性心脏病(IHD)对空气污染的易感性中的作用。在一项随机交叉研究中,40名健康成年人、40名COPD成年人和39名IHD成年人在污染较严重的街道或污染较轻的公园散步2小时。我们测量了行走前和行走后24小时尿液NO2-cLA,以及呼吸炎症生物标志物、肺功能、气道阻力和动脉僵硬度。COPD参与者的基线NO2-cLA水平是健康参与者的2.56倍(95% CI: 1.20-5.43),这可以解释为呼出一氧化氮和痰中髓过氧化物酶水平较高。在COPD但非健康或IHD参与者中,与公园相比,街道行走导致NO2-cLA水平下降57.7% (95% CI: 7.6-80.6%),痰生物标志物变化表明中性粒细胞炎症减少和缓解反应。NO2-cLA水平下降与暴露于黑碳和超细颗粒以及肺功能和动脉僵硬恶化有关。综上所述,硝化脂肪酸部分介导COPD患者对空气污染的心肺反应,解释了其易感性。
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来源期刊
Environment & Health
Environment & Health 环境科学、健康科学-
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期刊介绍: Environment & Health a peer-reviewed open access journal is committed to exploring the relationship between the environment and human health.As a premier journal for multidisciplinary research Environment & Health reports the health consequences for individuals and communities of changing and hazardous environmental factors. In supporting the UN Sustainable Development Goals the journal aims to help formulate policies to create a healthier world.Topics of interest include but are not limited to:Air water and soil pollutionExposomicsEnvironmental epidemiologyInnovative analytical methodology and instrumentation (multi-omics non-target analysis effect-directed analysis high-throughput screening etc.)Environmental toxicology (endocrine disrupting effect neurotoxicity alternative toxicology computational toxicology epigenetic toxicology etc.)Environmental microbiology pathogen and environmental transmission mechanisms of diseasesEnvironmental modeling bioinformatics and artificial intelligenceEmerging contaminants (including plastics engineered nanomaterials etc.)Climate change and related health effectHealth impacts of energy evolution and carbon neutralizationFood and drinking water safetyOccupational exposure and medicineInnovations in environmental technologies for better healthPolicies and international relations concerned with environmental health
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