Department of Respiratory and Critical Care Medicine, Beijing Chaoyang Hospital, Capital Medical University, Beijing, People's Republic of China.
Department of Respiratory and Critical Care Medicine, Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.
Int J Chron Obstruct Pulmon Dis. 2022 Jun 3;17:1299-1310. doi: 10.2147/COPD.S361929. eCollection 2022.
Fibrinogen is increasingly being studied as an inflammatory biomarker in chronic obstructive pulmonary disease (COPD), but there are limited data on the role of fibrinogen in assessing the severity of acute exacerbation of COPD (AECOPD). This study aimed to explore whether circulating fibrinogen could be used as a surrogate to measure the severity and predict the prognosis of AECOPD.
A total of 535 AECOPD patients diagnosed at our center from January 2016 to June 2021 were retrospectively enrolled in this study. The electronic medical record of each patient was retrieved to collect data on baseline characteristics and laboratory parameters, as well as the use of noninvasive positive-pressure ventilation (NPPV) and prognosis. Multiple linear regression analysis was used to identify independent factors associated with circulating fibrinogen values. Receiver-operating characteristic curve and multivariate logistic regression analysis were applied to further verify the use of fibrinogen to predict NPPV failure.
Compared to patients with fibrinogen <4 g/L, patients with increased fibrinogen levels (>4 g/L) tended to have elevated inflammatory response and higher incidence of DVT/PTE, emphysema, pneumonia, and atherosclerosis. In addition, fibrinogen levels in NPPV-failure patients were significantly higher than non-NPPV patients and NPPV-success ones. The presence of emphysema, pneumonia, and history of long-term oxygen therapy and higher CRP levels and leukocyte counts were independent risk factors associated with increased fibrinogen levels in AECOPD. Furthermore, our data indicated that fibrinogen could be considered as a reliable biomarker to predict NPPV failure (AUC, 0.899, 95% CI 0.846-0.952), with an OR of 7.702 (95% CI 2.984-19.875; <0.001).
The level of circulating fibrinogen can be used to measure severity of AECOPD, and among AECOPD patients managed with NPPV, fibrinogen >3.55 g/L can independently predict NPPV failure.
纤维蛋白原作为一种炎症生物标志物,在慢性阻塞性肺疾病(COPD)中的研究日益增多,但关于纤维蛋白原在评估 COPD 急性加重(AECOPD)严重程度中的作用的数据有限。本研究旨在探讨循环纤维蛋白原是否可作为衡量 AECOPD 严重程度和预测预后的替代指标。
回顾性纳入 2016 年 1 月至 2021 年 6 月期间在我院诊断为 AECOPD 的 535 例患者。检索每位患者的电子病历,收集基线特征和实验室参数、无创正压通气(NPPV)的应用和预后数据。采用多元线性回归分析确定与循环纤维蛋白原值相关的独立因素。应用受试者工作特征曲线和多因素逻辑回归分析进一步验证纤维蛋白原预测 NPPV 失败的作用。
与纤维蛋白原<4 g/L 的患者相比,纤维蛋白原水平升高(>4 g/L)的患者炎症反应更为明显,深静脉血栓形成/肺栓塞、肺气肿、肺炎和动脉粥样硬化的发生率更高。此外,NPPV 失败患者的纤维蛋白原水平明显高于非 NPPV 患者和 NPPV 成功患者。肺气肿、肺炎、长期氧疗史、较高的 C 反应蛋白和白细胞计数是 AECOPD 患者纤维蛋白原水平升高的独立危险因素。此外,我们的数据表明,纤维蛋白原可作为预测 NPPV 失败的可靠生物标志物(AUC,0.899,95%CI 0.846-0.952),OR 为 7.702(95%CI 2.984-19.875;<0.001)。
循环纤维蛋白原水平可用于衡量 AECOPD 的严重程度,在接受 NPPV 治疗的 AECOPD 患者中,纤维蛋白原>3.55 g/L 可独立预测 NPPV 失败。