Huang Xinmei, Balasubramanian Aparna, Moutchia Jude, Williams Kayleen, Al-Naamani Nadine, Batson Melissa, Gassett Amanda J, Minhas Jasleen, Kaufman Joel D, Leary Peter J, McCormick Meredith C, Mathai Stephen C, Kawut Steven M, Sack Coralynn
Department of Environmental and Occupational Health Sciences, School of Public Health.
Division of Pulmonary and Critical Care Medicine, Johns Hopkins University, Baltimore, Maryland; and.
Ann Am Thorac Soc. 2025 Sep;22(9):1351-1360. doi: 10.1513/AnnalsATS.202501-129OC.
The effects of long-term ambient air pollution exposure on survival in pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH) remain unclear. To evaluate the association between exposure to particulate matter with aerodynamic diameter ≤ 2.5 μm (PM), NO, and O and mortality or lung transplant in the Pulmonary Hypertension Association Registry (PHAR). A total of 2,196 adult patients enrolled in the PHAR provided data between 2015 and 2024. Annual average concentrations of air pollutants, including PM, NO, and O, estimated from validated spatiotemporal models in 2015 were linked to each participant's residential address. Cox proportional hazards models evaluated the associations between air pollutant exposures and risk of death or lung transplant, adjusting for baseline demographics, individual and neighborhood socioeconomic factors, disease severity, and spatial confounders. Additional analyses were adjusted for and stratified by nine U.S. census divisions. Study participants were broadly distributed across U.S. regions, with 72.0% female and a mean age of 55.7 years. A proportion of 35.6% had idiopathic PAH, 26.5% had connective tissue disease-associated PAH, and 14.5% had CTEPH. In models adjusted for demographics and individual and neighborhood socioeconomic factors, each interquartile range increase of PM was associated with a mortality or lung transplant hazard ratio of 1.16 (95% confidence interval, 1.01-1.33). This association was marginally attenuated and not statistically significant after adjusting for spatial covariates, with a hazard ratio of 1.12 (95% confidence interval, 0.95-1.31) per interquartile range increase in PM. We noted regional variation in the observed associations. No significant associations were found with NO or O. Long-term ambient air pollution exposure was not significantly associated with survival in PHAR patients with PAH or CTEPH. Future research should investigate potential modifying effects of regional social determinants and healthcare-related factors on the relationship between air pollution exposure and mortality in these conditions.
长期暴露于环境空气污染对肺动脉高压(PAH)和慢性血栓栓塞性肺动脉高压(CTEPH)患者生存的影响尚不清楚。为了评估在肺动脉高压协会注册中心(PHAR)中,暴露于空气动力学直径≤2.5μm的颗粒物(PM)、NO和O与死亡率或肺移植之间的关联。共有2196名成年患者参与了PHAR,他们提供了2015年至2024年的数据。根据2015年经过验证的时空模型估算的包括PM、NO和O在内的空气污染物年平均浓度与每位参与者的居住地址相关联。Cox比例风险模型评估了空气污染物暴露与死亡或肺移植风险之间的关联,并对基线人口统计学、个体和邻里社会经济因素、疾病严重程度以及空间混杂因素进行了调整。额外的分析根据美国九个普查区进行了调整和分层。研究参与者广泛分布于美国各地区,女性占72.0%,平均年龄为55.7岁。35.6%的患者患有特发性PAH,26.5%的患者患有结缔组织病相关性PAH,14.5%的患者患有CTEPH。在对人口统计学、个体和邻里社会经济因素进行调整的模型中,PM每增加一个四分位数间距,死亡率或肺移植风险比为1.16(95%置信区间,1.01 - 1.33)。在对空间协变量进行调整后,这种关联略有减弱且无统计学意义,PM每增加一个四分位数间距,风险比为1.12(95%置信区间,0.95 - 1.31)。我们注意到观察到的关联存在区域差异。未发现与NO或O有显著关联。长期暴露于环境空气污染与PHAR中PAH或CTEPH患者的生存无显著关联。未来的研究应调查区域社会决定因素和医疗相关因素对这些情况下空气污染暴露与死亡率之间关系的潜在调节作用。