Alladina Jehan W, Giacona Francesca L, Haring Alexis M, Hibbert Kathryn A, Medoff Benjamin D, Schmidt Eric P, Thompson Taylor, Maron Bradley A, Alba George A
Division of Pulmonary and Critical Care Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA.
Department of Medicine; University of Maryland School of Medicine, Baltimore, University of Maryland-Institute for Health Computing, Bethesda, MD.
CHEST Crit Care. 2024 Jun;2(2). doi: 10.1016/j.chstcc.2024.100054. Epub 2024 Feb 3.
The association of plasma biomarkers and clinical outcomes in ARDS resulting from SARS-CoV-2 infection predate the evidence-based use of immunomodulators.
Which plasma biomarkers are associated with clinical outcomes in patients with ARDS resulting from SARS-CoV-2 infection treated routinely with immunomodulators?
We collected plasma from patients with ARDS resulting from SARS-CoV-2 infection within 24 h of admission to the ICU between December 2020 and March 2021 (N = 69). We associated 16 total biomarkers of inflammation (eg, IL-6), coagulation (eg, D-dimer), epithelial injury (eg, surfactant protein D), and endothelial injury (eg, angiopoietin-2) with the primary outcome of in-hospital mortality and secondary outcome of ventilatory ratio (at baseline and day 3).
Thirty patients (43.5%) died within 60 days. All patients received corticosteroids and 6% also received tocilizumab. Compared with survivors, nonsurvivors demonstrated a higher baseline modified Sequential Organ Failure Assessment score (median, 8.5 [interquartile range (IQR), 7-9] vs 7 [IQR, 5-8]); = .004), lower Pao to Fio ratio (median, 153 [IQR, 118-182] vs 184 [IQR, 142-247]; = .04), and higher ventilatory ratio (median, 2.0 [IQR, 1.9-2.3] vs 1.5 [IQR, 1.4-1.9]; < .001). No difference was found in inflammatory, coagulation, or epithelial biomarkers between groups. Nonsurvivors showed higher median neural precursor cell expressed, developmentally down-regulated 9 (NEDD9) levels (median, 8.4 ng/mL [IQR, 7.0-11.2 ng/mL] vs 6.9 ng/mL [IQR, 5.5-8.0 ng/mL]; = .0025), von Willebrand factor domain A2 levels (8.7 ng/mL [IQR, 7.9-9.7 ng/mL] vs 6.5 ng/mL [IQR, 5.7-8.7 ng/mL]; = .007), angiopoietin-2 levels (9.0 ng/mL [IQR, 7.9-14.1 ng/mL] vs 7.0 ng/mL [IQR, 5.6-10.6 ng/mL]; = .01), and syndecan-1 levels (15.9 ng/mL [IQR, 14.5-17.5 ng/mL] vs 12.6 ng/mL [IQR, 10.5-16.1 ng/mL]; = .01). Only NEDD9 level met the adjusted threshold for significance ( < .003). Plasma NEDD9 level was associated with 60-day mortality (adjusted OR, 9.7; 95% CI, 1.6-60.4; = .015). Syndecan-1 level correlated with both baseline (ρ = 0.4; = .001) and day 3 ventilatory ratio (ρ = 0.5; < .001).
Biomarkers of inflammation, coagulation, and epithelial injury were not associated with clinical outcomes in a small cohort of patients with ARDS uniformly treated with immunomodulators. However, endothelial biomarkers, including plasma NEDD9, were associated with 60-day mortality.
在基于证据使用免疫调节剂之前,血浆生物标志物与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染所致急性呼吸窘迫综合征(ARDS)临床结局之间的关联就已存在。
在接受免疫调节剂常规治疗的SARS-CoV-2感染所致ARDS患者中,哪些血浆生物标志物与临床结局相关?
我们收集了2020年12月至2021年3月期间入住重症监护病房(ICU)24小时内的SARS-CoV-2感染所致ARDS患者的血浆(N = 69)。我们将16种炎症(如白细胞介素-6)、凝血(如D-二聚体)、上皮损伤(如表面活性蛋白D)和内皮损伤(如血管生成素-2)的生物标志物与院内死亡的主要结局及通气比的次要结局(基线和第3天)进行关联分析。
30例患者(43.5%)在60天内死亡。所有患者均接受了皮质类固醇治疗,6%的患者还接受了托珠单抗治疗。与幸存者相比,非幸存者的基线改良序贯器官衰竭评估评分更高(中位数,8.5[四分位间距(IQR),7 - 9]对7[IQR,5 - 8];P = 0.004),氧合指数(Pao₂/Fio₂)更低(中位数,153[IQR,118 - 182]对184[IQR,142 - 247];P = 0.04),通气比更高(中位数,2.0[IQR,1.9 - 2.3]对1.5[IQR,1.4 - 1.9];P < 0.001)。两组间炎症、凝血或上皮生物标志物无差异。非幸存者的神经前体细胞表达、发育下调9(NEDD9)水平更高(中位数,8.4 ng/mL[IQR,7.0 - 11.2 ng/mL]对6.9 ng/mL[IQR,5.5 - 8.0 ng/mL];P = 0.0025),血管性血友病因子A2结构域水平更高(8.7 ng/mL[IQR,7.9 - 9.7 ng/mL]对6.5 ng/mL[IQR,5.7 - 8.7 ng/mL];P = 0.007);血管生成素-2水平更高(9.0 ng/mL[IQR,7.9 - 14.1 ng/mL]对7.0 ng/mL[IQR,5.6 - 10.6 ng/mL];P = 0.01),多配体蛋白聚糖-1水平更高(15.9 ng/mL[IQR,14.5 - 17.5 ng/mL]对12.6 ng/mL[IQR,10.5 - 16.1 ng/mL];P = 0.01)。只有NEDD9水平达到调整后的显著性阈值(P < 0.003)。血浆NEDD9水平与60天死亡率相关(调整后比值比,9.7;95%置信区间,1.6 - 60.4;P = 0.015)。多配体蛋白聚糖-1水平与基线(ρ = 0.4;P = 0.001)和第3天通气比均相关(ρ = 0.5;P < 0.001)。
在一小群接受免疫调节剂统一治疗的ARDS患者中,炎症、凝血和上皮损伤的生物标志物与临床结局无关。然而,包括血浆NEDD9在内的内皮生物标志物与60天死亡率相关。