Department of Thoracic Medicine and Surgery, Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania, United States of America.
FLUIDDA, Inc., New York, New York, United States of America.
PLoS One. 2021 Oct 15;16(10):e0257892. doi: 10.1371/journal.pone.0257892. eCollection 2021.
Coronavirus Disease 2019 (COVID-19) is a respiratory viral illness causing pneumonia and systemic disease. Abnormalities in pulmonary function tests (PFT) after COVID-19 infection have been described. The determinants of these abnormalities are unclear. We hypothesized that inflammatory biomarkers and CT scan parameters at the time of infection would be associated with abnormal gas transfer at short term follow-up.
We retrospectively studied subjects who were hospitalized for COVID-19 pneumonia and discharged. Serum inflammatory biomarkers, CT scan and clinical characteristics were assessed. CT images were evaluated by Functional Respiratory Imaging with automated tissue segmentation algorithms of the lungs and pulmonary vasculature. Volumes of the pulmonary vessels that were ≤5mm (BV5), 5-10mm (BV5_10), and ≥10mm (BV10) in cross sectional area were analyzed. Also the amount of opacification on CT (ground glass opacities). PFT were performed 2-3 months after discharge. The diffusion capacity of carbon monoxide (DLCO) was obtained. We divided subjects into those with a DLCO <80% predicted (Low DLCO) and those with a DLCO ≥80% predicted (Normal DLCO).
38 subjects were included in our cohort. 31 out of 38 (81.6%) subjects had a DLCO<80% predicted. The groups were similar in terms of demographics, body mass index, comorbidities, and smoking status. Hemoglobin, inflammatory biomarkers, spirometry and lung volumes were similar between groups. CT opacification and BV5 were not different between groups, but both Low and Normal DLCO groups had lower BV5 measures compared to healthy controls. BV5_10 and BV10 measures were higher in the Low DLCO group compared to the normal DLCO group. Both BV5_10 and BV10 in the Low DLCO group were greater compared to healthy controls. BV5_10 was independently associated with DLCO<80% in multivariable logistic regression (OR 1.29, 95% CI 1.01, 1.64). BV10 negatively correlated with DLCO% predicted (r = -0.343, p = 0.035).
Abnormalities in pulmonary vascular volumes at the time of hospitalization are independently associated with a low DLCO at follow-up. There was no relationship between inflammatory biomarkers during hospitalization and DLCO. Pulmonary vascular abnormalities during hospitalization for COVID-19 may serve as a biomarker for abnormal gas transfer after COVID-19 pneumonia.
2019 年冠状病毒病(COVID-19)是一种呼吸道病毒病,可引起肺炎和全身疾病。COVID-19 感染后肺功能测试(PFT)异常已有描述。这些异常的决定因素尚不清楚。我们假设感染时的炎症生物标志物和 CT 扫描参数与短期随访时的气体转移异常有关。
我们回顾性研究了因 COVID-19 肺炎住院并出院的患者。评估了血清炎症生物标志物、CT 扫描和临床特征。使用肺部和肺血管的自动组织分割算法的功能呼吸成像评估 CT 图像。分析了横截面积中≤5mm(BV5)、5-10mm(BV5_10)和≥10mm(BV10)的肺血管体积。还分析了 CT 上的混浊量(磨玻璃混浊)。出院后 2-3 个月进行 PFT。获得一氧化碳弥散量(DLCO)。我们将患者分为 DLCO<80%预测值(低 DLCO)和 DLCO≥80%预测值(正常 DLCO)。
我们的队列纳入了 38 例患者。38 例患者中有 31 例(81.6%)的 DLCO<80%预测值。两组在人口统计学、体重指数、合并症和吸烟状况方面相似。两组的血红蛋白、炎症生物标志物、肺量计和肺容积相似。CT 混浊和 BV5 在两组之间无差异,但低 DLCO 组和正常 DLCO 组的 BV5 测量值均低于健康对照组。低 DLCO 组的 BV5_10 和 BV10 测量值高于正常 DLCO 组。低 DLCO 组的 BV5_10 和 BV10 均高于健康对照组。在多变量逻辑回归中,BV5_10 与 DLCO<80%独立相关(OR 1.29,95%CI 1.01,1.64)。BV10 与 DLCO%预测值呈负相关(r=-0.343,p=0.035)。
住院时肺血管容积的异常与随访时的低 DLCO 独立相关。住院期间的炎症生物标志物与 DLCO 无关系。COVID-19 住院期间的肺血管异常可能是 COVID-19 肺炎后气体转移异常的生物标志物。