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与抗炎治疗的新型冠状病毒肺炎所致急性呼吸窘迫综合征中通气比和死亡率相关的内皮功能障碍循环生物标志物

Circulating Biomarkers of Endothelial Dysfunction Associated With Ventilatory Ratio and Mortality in ARDS Resulting From SARS-CoV-2 Infection Treated With Antiinflammatory Therapies.

作者信息

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

机构信息

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.

出版信息

CHEST Crit Care. 2024 Jun;2(2). doi: 10.1016/j.chstcc.2024.100054. Epub 2024 Feb 3.

DOI:10.1016/j.chstcc.2024.100054
PMID:39035722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11259037/
Abstract

BACKGROUND

The association of plasma biomarkers and clinical outcomes in ARDS resulting from SARS-CoV-2 infection predate the evidence-based use of immunomodulators.

RESEARCH QUESTION

Which plasma biomarkers are associated with clinical outcomes in patients with ARDS resulting from SARS-CoV-2 infection treated routinely with immunomodulators?

STUDY DESIGN AND METHODS

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).

RESULTS

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).

INTERPRETATION

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.

摘要

背景

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。

研究问题

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?

研究设计与方法

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。

结果

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)。

解读

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5bb/11259037/a681090f2986/nihms-2004319-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5bb/11259037/6085a22f0848/nihms-2004319-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5bb/11259037/ba30e7d546f6/nihms-2004319-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5bb/11259037/1cbbe87debc7/nihms-2004319-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5bb/11259037/a681090f2986/nihms-2004319-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5bb/11259037/6085a22f0848/nihms-2004319-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5bb/11259037/ba30e7d546f6/nihms-2004319-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5bb/11259037/1cbbe87debc7/nihms-2004319-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5bb/11259037/a681090f2986/nihms-2004319-f0004.jpg

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