Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University Hospital, Seoul, 03080, Republic of Korea.
Department of Internal Medicine, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Respir Res. 2021 Nov 20;22(1):297. doi: 10.1186/s12931-021-01878-7.
Despite the high disease burden of chronic obstructive pulmonary disease (COPD) and risk of acute COPD exacerbation, few COPD biomarkers are available. As developmental endothelial locus-1 (DEL-1) has been proposed to possess beneficial effects, including anti-inflammatory effects, we hypothesized that DEL-1 could be a blood biomarker for COPD.
To elucidate the role of plasma DEL-1 as a biomarker of COPD in terms of pathogenesis and for predicting acute exacerbation.
Cigarette smoke extract (CSE) or saline was intratracheally administered to wild-type (WT) and DEL-1 knockout (KO) C57BL/6 mice. Subsequently, lung sections were obtained to quantify the degree of emphysema using the mean linear intercept (MLI). Additionally, plasma DEL-1 levels were compared between COPD and non-COPD participants recruited in ongoing prospective cohorts. Using negative binomial regression analysis, the association between the plasma DEL-1 level and subsequent acute exacerbation risk was evaluated in patients with COPD.
In the in vivo study, DEL-1 KO induced emphysema (KO saline vs. WT saline; P = 0.003) and augmented CSE-induced emphysema (KO CSE vs. WT CSE; P < 0.001) in 29 mice. Among 537 participants, patients with COPD presented plasma log (DEL-1) levels lower than non-COPD participants (P = 0.04), especially non-COPD never smokers (P = 0.019). During 1.2 ± 0.3 years, patients with COPD in the lowest quartile of Log(DEL-1) demonstrated an increased risk of subsequent acute exacerbation, compared with those in the highest quartile of Log(DEL-1) (adjusted incidence rate ratio, 3.64; 95% confidence interval, 1.03-12.9).
Low DEL-1 levels are associated with COPD development and increased risk of subsequent COPD acute exacerbation. DEL-1 can be a useful biomarker in patients with COPD.
尽管慢性阻塞性肺疾病(COPD)的疾病负担很高,且急性 COPD 加重的风险很大,但目前可用的 COPD 生物标志物却很少。由于发育内皮基因座-1(DEL-1)具有抗炎等有益作用,我们假设 DEL-1 可能是 COPD 的血液生物标志物。
从发病机制和预测急性加重的角度阐明血浆 DEL-1 作为 COPD 生物标志物的作用。
用香烟烟雾提取物(CSE)或生理盐水对野生型(WT)和 DEL-1 敲除(KO)C57BL/6 小鼠进行气管内给药。随后,获取肺组织切片,使用平均线性截距(MLI)量化肺气肿程度。此外,比较了正在进行的前瞻性队列中 COPD 和非 COPD 参与者的血浆 DEL-1 水平。采用负二项回归分析评估 COPD 患者血浆 DEL-1 水平与随后急性加重风险之间的关系。
在体内研究中,DEL-1 KO 诱导肺气肿(KO 生理盐水与 WT 生理盐水相比;P = 0.003),并增强 CSE 诱导的肺气肿(KO CSE 与 WT CSE 相比;P < 0.001),共涉及 29 只小鼠。在 537 名参与者中,与非 COPD 参与者相比,COPD 患者的血浆 log(DEL-1)水平较低(P = 0.04),尤其是非 COPD 从不吸烟者(P = 0.019)。在 1.2±0.3 年内,与 Log(DEL-1)最高四分位的患者相比,Log(DEL-1)最低四分位的 COPD 患者发生后续急性加重的风险增加(调整后发病率比,3.64;95%置信区间,1.03-12.9)。
低 DEL-1 水平与 COPD 发生和随后 COPD 急性加重风险增加相关。DEL-1 可作为 COPD 患者的有用生物标志物。