Effect of High Altitude on Small Pulmonary Vein and Artery Volume in the COPDGene Cohort: Towards Better Understanding of Lung Physiology and Pulmonary Disease.
Anastasia K A L Kwee, Esther Pompe, Leticia Gallardo Estrella, Jean-Paul Charbonnier, Stephen M Humphries, Harm A W M Tiddens, James D Crapo, Richard Casaburi, Pim A de Jong, David A Lynch, Firdaus A A Mohamed Hoesein
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引用次数: 0
Abstract
Background: To personalize the care for persons with smoking-related lung disease, a thorough understanding of its etiology is essential. The role of pulmonary vessels remains poorly understood. Living at high altitude provides a natural model to investigate the effects of low oxygen levels on pulmonary vessels. This study aims to evaluate the relationship between living at high altitudes and small pulmonary vein and artery volumes. We hypothesize that small vein and artery volumes were independently associated with living at high altitude. Methods: We quantified small pulmonary vein and artery dimensions (ᴓ < 1 mm) on computed tomography (CT) down to 0.2 mm in diameter and normalized the dimensions by body surface area. In 8931 current and former smokers participating in the COPDGene study, we used multivariate regression models corrected for clinical and technical confounders. Results: 1262 residents (14.1%) were defined as high-altitude residents (~1600 m, Denver, CO, USA). Compared to lower-altitude residents, the high-altitude residents had a higher age (62.0 ± 9.1 vs. 59.6 ± 9.0 years), more pack-years smoked (46.8 vs. 44.1) and a lower FEV1% predicted (64.6 ± 32.4% vs. 76.8 ± 25.2%). Both mean small artery volume (4.09 ± 0.89 mL/m2 vs. 3.85 ± 0.90 mL/m2) and mean small vein volume (2.96 ± 0.53 mL/m2 vs. 2.67 ± 0.53 mL/m2) were higher in high-altitude residents. Multivariate linear regression showed that, in those without COPD, high-altitude residents have a higher small vein volume (0.129 mL/m2, p < 0.001) and higher small artery volume (0.170 mL/m2, p = 0.001) compared to lower-altitude residents. There was no significant association in residents with COPD. Conclusions: In current and former smokers without COPD, higher small pulmonary vein and artery volumes were associated with living at high altitude, independent of lung disease or technical CT parameters. A potential cause includes vascular remodeling due to an elevated need for blood oxygen transport, which becomes concealed when COPD develops.
背景:为了对吸烟相关肺部疾病患者进行个性化护理,深入了解其病因是必不可少的。肺血管的作用仍然知之甚少。生活在高海拔地区为研究低氧水平对肺血管的影响提供了一个自然模型。本研究旨在评估生活在高海拔地区与肺静脉和动脉体积小之间的关系。我们假设静脉和动脉体积小与生活在高海拔地区独立相关。方法:在计算机断层扫描(CT)上量化小肺静脉和动脉( < 1mm)的尺寸(直径小于0.2 mm),并按体表面积归一化尺寸。在参与COPDGene研究的8931名吸烟者和戒烟者中,我们使用了校正临床和技术混杂因素的多变量回归模型。结果:1262人(14.1%)被定义为高海拔居民(~1600 m, Denver, CO, USA)。与低海拔地区居民相比,高海拔地区居民的年龄(62.0±9.1岁)高于低海拔地区居民(59.6±9.0岁),吸烟包年(46.8年)高于低海拔地区居民(44.1年),预测FEV1%低于低海拔地区居民(64.6±32.4%)。高海拔地区居民的平均小动脉体积(4.09±0.89 mL/m2 vs. 3.85±0.90 mL/m2)和平均小静脉体积(2.96±0.53 mL/m2 vs. 2.67±0.53 mL/m2)均较高。多元线性回归结果显示,在非COPD患者中,高原居民的小静脉体积(0.129 mL/m2, p < 0.001)和小动脉体积(0.170 mL/m2, p = 0.001)均高于低海拔居民。在COPD患者中没有明显的相关性。结论:在目前和以前没有COPD的吸烟者中,较高的小肺静脉和动脉体积与生活在高海拔地区有关,与肺部疾病或技术CT参数无关。一个潜在的原因包括由于血氧运输需求的增加而引起的血管重构,当COPD发展时,血管重构被掩盖。
期刊介绍:
Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.