Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA
GSK Research and Development, King of Prussia, PA, USA.
Eur Respir J. 2018 Feb 7;51(2). doi: 10.1183/13993003.02146-2017. Print 2018 Feb.
We tested whether emphysema progression accompanies enhanced tissue loss in other body compartments in 1817 patients from the ECLIPSE chronic obstructive pulmonary disease (COPD) cohort.Clinical and selected systemic biomarker measurements were compared in subjects grouped by quantitative tomography scan emphysema quartiles using the percentage of low attenuation area (LAA%). Lowest and highest quartile patients had amino-acid metabolomic profiles. We related LAA% to 3 years decline in lung function (forced expiratory volume in 1 s (FEV)), body mass index (BMI), fat-free mass index (FFMI) and exacerbations, hospitalisations and mortality rates.Participants with more baseline emphysema had lower FEV, BMI and FFMI, worse functional capacity, and less cardiovascular disease but more osteoporosis. Systemic C-reactive protein and interleukin-6 levels were similar among groups, but club cell protein 16 was higher and interleukin-8, surfactant protein D and soluble receptor for advanced glycation end product were lower with more emphysema. Metabolomics differed between extreme emphysema quartiles. Patients with more emphysema had accelerated FEV, BMI and FFMI decline and more exacerbations, hospitalisations and mortality.COPD patients with more emphysema undergo excessive loss of pulmonary and extrapulmonary tissue, which is probably related to abnormal tissue maintenance. Because of worse clinical outcomes, we propose this subgroup be named the multi-organ loss of tissue (MOLT) COPD phenotype.
我们在 ECLIPSE 慢性阻塞性肺疾病(COPD)队列中对 1817 名患者进行了测试,以观察肺气肿进展是否伴随着其他身体部位组织损失的增加。通过定量 CT 扫描肺气肿四分位组比较了临床和选定的系统生物标志物测量值,使用低衰减区(LAA%)的百分比。最低和最高四分位患者的氨基酸代谢组学特征不同。我们将 LAA%与肺功能(1 秒用力呼气量(FEV))、体重指数(BMI)、去脂体重指数(FFMI)和恶化、住院和死亡率的 3 年下降相关联。基线肺气肿程度较高的患者的 FEV、BMI 和 FFMI 较低,功能能力较差,心血管疾病较少,但骨质疏松症较多。各组间的全身 C 反应蛋白和白细胞介素-6 水平相似,但肺气肿程度较高时,细胞蛋白 16 较高,白细胞介素-8、表面活性蛋白 D 和晚期糖基化终产物可溶性受体较低。代谢组学在极端肺气肿四分位之间存在差异。肺气肿程度较高的患者的 FEV、BMI 和 FFMI 下降加速,恶化、住院和死亡率增加。患有更多肺气肿的 COPD 患者会经历过度的肺和肺外组织损失,这可能与异常的组织维持有关。由于较差的临床结果,我们建议将这一组命名为多器官组织损失(MOLT)COPD 表型。