Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Department of Medicine, University of California, San Francisco, CA, USA.
Environ Int. 2020 Aug;141:105780. doi: 10.1016/j.envint.2020.105780. Epub 2020 May 8.
Chronic air pollutant exposure has been associated with development of Acute Respiratory Distress Syndrome (ARDS) in patients at risk, particularly from severe trauma. We recently reported that shorter peripheral blood leukocyte (PBL) telomere length (TL) was associated with worse outcomes and higher severity of ARDS in critically ill patients. Since most major air pollutants are potent oxidants that can induce cellular oxidative stress, and oxidative stress can accelerate telomere shortening, we hypothesized that higher levels of chronic air pollutant exposure would be associated with shorter telomere length in critically ill patients including patients with ARDS.
PBL-TL was measured in genomic DNA collected on the morning of ICU day 2 in 772 critically ill patients enrolled in a prospective observational study. Exposures to air pollutants including ozone (warm-season only), particulate matter < 2.5 µm (PM), particulate matter < 10 µm (PM), CO, NO and SO, were estimated by weighted average of daily levels from all monitors within 50 km of each patient's residential address for the 3 years prior to admission. Associations of each air pollutant exposure and PBL-TL were investigated by multivariable linear regression models adjusting for age, ethnicity, sex, smoking history, alcohol abuse, insurance status, median household income, history of malignancy and APACHE II.
Contrary to our hypothesis, TL increased across exposure quartiles in both ozone and PM analyses (p < 0.05). In a regression model controlling for potential confounders, long term ozone exposure was significantly associated with an increase in TL in the entire cohort (0.31 kb per 10 ppb), as well as in subgroups with sepsis, trauma and ARDS (all p < 0.05). In multivariable models, entire-year exposure to PM, PM, CO, NO and SO was not associated with TL after adjustment for potential confounders. In an analysis restricted to warm-season levels to assess the effect of seasonality, higher warm-season PM and CO exposures were independently associated with longer TL.
Long-term exposure to ozone is associated with longer peripheral blood TL in critically ill patients. Further studies are needed to investigate the potential underlying mechanisms for this unexpected positive association between telomere length and air pollution exposure in critical illness.
慢性空气污染物暴露与高危患者急性呼吸窘迫综合征(ARDS)的发展有关,尤其是严重创伤患者。我们最近报道称,外周血白细胞(PBL)端粒长度(TL)较短与危重病患者的预后较差和 ARDS 严重程度较高有关。由于大多数主要空气污染物都是很强的氧化剂,会导致细胞氧化应激,而氧化应激会加速端粒缩短,我们假设慢性空气污染物暴露水平较高与危重病患者(包括 ARDS 患者)的端粒长度较短有关。
在一项前瞻性观察性研究中,对入住 ICU 第 2 天早上采集的 772 名危重病患者的基因组 DNA 进行 PBL-TL 测量。通过加权平均法,根据患者入院前 3 年每个患者居住地址 50km 范围内所有监测器的日水平,估算了臭氧(仅限暖季)、<2.5μm 颗粒物(PM)、<10μm 颗粒物(PM)、CO、NO 和 SO 等空气污染物的暴露量。通过多变量线性回归模型,在调整年龄、种族、性别、吸烟史、酗酒史、保险状况、中位数家庭收入、恶性肿瘤病史和急性生理学与慢性健康状况评分系统(APACHE II)后,研究了每种空气污染物暴露与 PBL-TL 的关系。
与我们的假设相反,臭氧和 PM 分析中 TL 随着暴露四分位数的增加而增加(p<0.05)。在控制潜在混杂因素的回归模型中,长期臭氧暴露与整个队列的 TL 增加显著相关(每增加 10ppb 增加 0.31kb),以及败血症、创伤和 ARDS 亚组也显著相关(均 p<0.05)。在多变量模型中,在调整潜在混杂因素后,整个年度 PM、PM、CO、NO 和 SO 暴露与 TL 无关。在一项分析中,限制在暖季水平以评估季节性的影响,较高的暖季 PM 和 CO 暴露与较长的 TL 独立相关。
长期暴露于臭氧与危重病患者的外周血 TL 较长有关。需要进一步研究来探讨这种在危重病中出乎意料的端粒长度与空气污染暴露之间的正相关关系的潜在机制。