Pistenmaa Carrie L, Hoffman Eric A, Prince Martin R, Hughes Emlyn, Dashnaw Stephen, Lo Cascio Christian M, Oelsner Elizabeth C, Shen Wei, Sun Yanping, Winther Hinrich, Vogel-Claussen Jens, Wild Jim M, Tracy Russell P, Barr R Graham
Columbia University, New York, NY, USA; Brigham and Women's Hospital, Boston, MA, USA.
University of Iowa, Iowa City, IA, USA.
Respir Med. 2025 May;241:108058. doi: 10.1016/j.rmed.2025.108058. Epub 2025 Mar 25.
The pulmonary vasculature has been implicated in chronic obstructive pulmonary disease (COPD). Whether platelet activation is associated with COPD-related characteristics is unknown.
The Multi-Ethnic Study of Atherosclerosis (MESA) COPD Study enrolled participants with 10+ pack-years with and without COPD from 2 cohort studies. Platelet activation was measured in platelet-free plasma as von Willebrand factor (vWF), beta-thromboglobulin (BTG) and platelet factor 4 (PF4). Phenotyping included spirometry, percent emphysema, air trapping on computed tomography (CT), low-ventilated lung volume on He-magnetic resonance imaging (MRI) and contrast-enhanced MRI pulmonary perfusion on and off oxygen. Linear and logistic regression adjusted for demographics, anthropometry, platelet count, aspirin use, COPD status and cohort; the final model adjusted for smoking, pack-years, oxygen saturation and hypertension.
The 116 with vWF were a mean age of 73.5 ± 7.3 years old, 60 % male, 58 % Non-Hispanic White, 28 % Black, 14 % Hispanic/Latino, 23 % smoked currently and 55 % had COPD. vWF was associated with lower FEV/FVC (-2.0 %/SD vWF, 95 %CI: -3.5, -0.6), and greater percent low-ventilated lung volume on He-MRI (6.5 %/SD vWF, 95 %CI: 1.5, 11.5), CT air trapping (3.2 %/SD vWF, 95 %CI: 1.4, 5.1) and heterogeneity (CV) of pulmonary microvascular blood flow (PMBF) and pulmonary microvascular blood volume (PMBV) on oxygen. Higher BTG and PF4 were associated with greater PMBF and PMBV. There was increased odds of COPD with higher PF4 (final model only: OR 1.8/SD PF4, 95 %CI: 1.01, 3.20).
Platelet activation was associated with measures of small airways disease and pulmonary microvascular perfusion in this sample of smokers with and without COPD.
肺血管系统与慢性阻塞性肺疾病(COPD)有关。血小板活化是否与COPD相关特征相关尚不清楚。
动脉粥样硬化多民族研究(MESA)COPD研究从2个队列研究中纳入了吸烟史≥10包年且患有或未患有COPD的参与者。在无血小板血浆中测量血小板活化情况,指标包括血管性血友病因子(vWF)、β-血小板球蛋白(BTG)和血小板因子4(PF4)。表型分析包括肺活量测定、肺气肿百分比、计算机断层扫描(CT)上的气体潴留、氦磁共振成像(MRI)上的低通气肺容积以及吸氧和不吸氧状态下的对比增强MRI肺灌注。采用线性回归和逻辑回归,并对人口统计学、人体测量学、血小板计数、阿司匹林使用情况、COPD状态和队列进行了校正;最终模型对吸烟、吸烟包年数、血氧饱和度和高血压进行了校正。
116例有vWF的参与者平均年龄为73.5±7.3岁,男性占60%,非西班牙裔白人占58%,黑人占28%,西班牙裔/拉丁裔占14%,23%为当前吸烟者,55%患有COPD。vWF与较低的FEV/FVC相关(vWF每标准差变化-2.0%,95%置信区间:-3.5,-0.6),且与氦MRI上更大的低通气肺容积百分比(vWF每标准差变化6.5%,95%置信区间:1.5,11.5)、CT气体潴留(vWF每标准差变化3.2%,95%置信区间:1.4,5.1)以及吸氧状态下肺微血管血流(PMBF)和肺微血管血容量(PMBV)的异质性(CV)相关。较高的BTG和PF4与更大的PMBF和PMBV相关。PF4水平较高时患COPD的几率增加(仅最终模型:PF4每标准差变化的比值比为1.8,95%置信区间:1.01,3.20)。
在这个有或无COPD的吸烟者样本中,血小板活化与小气道疾病和肺微血管灌注指标相关。