内皮功能障碍的循环生物标志物与接受抗炎治疗的 SARS-CoV-2 感染所致急性呼吸窘迫综合征患者的通气比率和死亡率有关

Jehan W. Alladina MD , Francesca L. Giacona BA , Alexis M. Haring BA , Kathryn A. Hibbert MD , Benjamin D. Medoff MD , Eric P. Schmidt MD , Taylor Thompson MD , Bradley A. Maron MD , George A. Alba MD
{"title":"内皮功能障碍的循环生物标志物与接受抗炎治疗的 SARS-CoV-2 感染所致急性呼吸窘迫综合征患者的通气比率和死亡率有关","authors":"Jehan W. Alladina MD ,&nbsp;Francesca L. Giacona BA ,&nbsp;Alexis M. Haring BA ,&nbsp;Kathryn A. Hibbert MD ,&nbsp;Benjamin D. Medoff MD ,&nbsp;Eric P. Schmidt MD ,&nbsp;Taylor Thompson MD ,&nbsp;Bradley A. Maron MD ,&nbsp;George A. Alba MD","doi":"10.1016/j.chstcc.2024.100054","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>The association of plasma biomarkers and clinical outcomes in ARDS resulting from SARS-CoV-2 infection predate the evidence-based use of immunomodulators.</p></div><div><h3>Research Question</h3><p>Which plasma biomarkers are associated with clinical outcomes in patients with ARDS resulting from SARS-CoV-2 infection treated routinely with immunomodulators?</p></div><div><h3>Study Design and Methods</h3><p>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).</p></div><div><h3>Results</h3><p>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]); <em>P</em> = .004), lower Pa<span>o</span><sub>2</sub> to F<span>io</span><sub>2</sub> ratio (median, 153 [IQR, 118-182] vs 184 [IQR, 142-247]; <em>P</em> = .04), and higher ventilatory ratio (median, 2.0 [IQR, 1.9-2.3] vs 1.5 [IQR, 1.4-1.9]; <em>P</em> &lt; .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]; <em>P</em> = .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]; <em>P</em> = .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]; <em>P</em> = .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]; <em>P</em> = .01). Only NEDD9 level met the adjusted threshold for significance (<em>P</em> &lt; .003). Plasma NEDD9 level was associated with 60-day mortality (adjusted OR, 9.7; 95% CI, 1.6-60.4; <em>P</em> = .015). Syndecan-1 level correlated with both baseline (ρ = 0.4; <em>P</em> = .001) and day 3 ventilatory ratio (ρ = 0.5; <em>P</em> &lt; .001).</p></div><div><h3>Interpretation</h3><p>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.</p></div>","PeriodicalId":93934,"journal":{"name":"CHEST critical care","volume":"2 2","pages":"Article 100054"},"PeriodicalIF":0.0000,"publicationDate":"2024-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S294978842400008X/pdfft?md5=35b37476cd22672e512be05ff829f5de&pid=1-s2.0-S294978842400008X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Circulating Biomarkers of Endothelial Dysfunction Associated With Ventilatory Ratio and Mortality in ARDS Resulting From SARS-CoV-2 Infection Treated With Antiinflammatory Therapies\",\"authors\":\"Jehan W. Alladina MD ,&nbsp;Francesca L. Giacona BA ,&nbsp;Alexis M. Haring BA ,&nbsp;Kathryn A. Hibbert MD ,&nbsp;Benjamin D. Medoff MD ,&nbsp;Eric P. Schmidt MD ,&nbsp;Taylor Thompson MD ,&nbsp;Bradley A. Maron MD ,&nbsp;George A. Alba MD\",\"doi\":\"10.1016/j.chstcc.2024.100054\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>The association of plasma biomarkers and clinical outcomes in ARDS resulting from SARS-CoV-2 infection predate the evidence-based use of immunomodulators.</p></div><div><h3>Research Question</h3><p>Which plasma biomarkers are associated with clinical outcomes in patients with ARDS resulting from SARS-CoV-2 infection treated routinely with immunomodulators?</p></div><div><h3>Study Design and Methods</h3><p>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).</p></div><div><h3>Results</h3><p>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]); <em>P</em> = .004), lower Pa<span>o</span><sub>2</sub> to F<span>io</span><sub>2</sub> ratio (median, 153 [IQR, 118-182] vs 184 [IQR, 142-247]; <em>P</em> = .04), and higher ventilatory ratio (median, 2.0 [IQR, 1.9-2.3] vs 1.5 [IQR, 1.4-1.9]; <em>P</em> &lt; .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]; <em>P</em> = .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]; <em>P</em> = .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]; <em>P</em> = .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]; <em>P</em> = .01). Only NEDD9 level met the adjusted threshold for significance (<em>P</em> &lt; .003). Plasma NEDD9 level was associated with 60-day mortality (adjusted OR, 9.7; 95% CI, 1.6-60.4; <em>P</em> = .015). Syndecan-1 level correlated with both baseline (ρ = 0.4; <em>P</em> = .001) and day 3 ventilatory ratio (ρ = 0.5; <em>P</em> &lt; .001).</p></div><div><h3>Interpretation</h3><p>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.</p></div>\",\"PeriodicalId\":93934,\"journal\":{\"name\":\"CHEST critical care\",\"volume\":\"2 2\",\"pages\":\"Article 100054\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-02-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S294978842400008X/pdfft?md5=35b37476cd22672e512be05ff829f5de&pid=1-s2.0-S294978842400008X-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"CHEST critical care\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S294978842400008X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"CHEST critical care","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S294978842400008X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

背景SARS-CoV-2感染导致的ARDS患者的血浆生物标志物与临床结局的关联早于免疫调节剂的循证使用。研究问题哪些血浆生物标志物与常规使用免疫调节剂治疗的SARS-CoV-2感染导致的ARDS患者的临床结局相关? 研究设计与方法我们在2020年12月至2021年3月期间收集了SARS-CoV-2感染导致的ARDS患者在入住ICU后24小时内的血浆(N = 69)。我们将炎症(如 IL-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 16 种总生物标记物与院内死亡率的主要结果和通气比(基线和第 3 天)的次要结果联系起来。所有患者都接受了皮质类固醇治疗,6%的患者还接受了托珠单抗治疗。与存活者相比,非存活者的基线修正器官功能衰竭评估评分更高(中位数为 8.5 [四分位数间距 (IQR),7-9] vs 7 [IQR, 5-8]);P = .004)、较低的 Pao2 与 Fio2 比率(中位数,153 [IQR, 118-182] vs 184 [IQR, 142-247];P = .04)和较高的通气比率(中位数,2.0 [IQR, 1.9-2.3] vs 1.5 [IQR, 1.4-1.9];P <.001)。各组之间的炎症、凝血或上皮生物标志物没有差异。非存活者的神经前体细胞表达、发育下调 9 (NEDD9) 水平中位数(中位数,8.4 ng/mL [IQR, 7.0-11.2 ng/mL] vs 6.9 ng/mL [IQR, 5.5-8.0 ng/mL];P = .0025)、von Willebrand 因子域 A2 水平(8.7 ng/mL [IQR, 7.9-9.7 ng/mL] vs 6.5 ng/mL [IQR, 5.7-8.7 ng/mL];P = .007)、血管生成素-2 水平(9.0 ng/mL [IQR, 7.9-14.1 ng/mL] vs 7.0 ng/mL [IQR, 5.6-10.6纳克/毫升];P = .01)和辛迪加-1水平(15.9纳克/毫升[IQR,14.5-17.5纳克/毫升] vs 12.6纳克/毫升[IQR,10.5-16.1纳克/毫升];P = .01)。只有 NEDD9 水平达到了调整后的显著性阈值(P < .003)。血浆 NEDD9 水平与 60 天死亡率相关(调整 OR,9.7;95% CI,1.6-60.4;P = .015)。Syndecan-1水平与基线(ρ = 0.4; P = .001)和第3天通气比率(ρ = 0.5; P < .001)相关。然而,包括血浆NEDD9在内的内皮生物标志物与60天死亡率有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circulating Biomarkers of Endothelial Dysfunction Associated With Ventilatory Ratio and Mortality in ARDS Resulting From SARS-CoV-2 Infection Treated With Antiinflammatory Therapies

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]); P = .004), lower Pao2 to Fio2 ratio (median, 153 [IQR, 118-182] vs 184 [IQR, 142-247]; P = .04), and higher ventilatory ratio (median, 2.0 [IQR, 1.9-2.3] vs 1.5 [IQR, 1.4-1.9]; P < .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]; P = .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]; P = .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]; P = .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]; P = .01). Only NEDD9 level met the adjusted threshold for significance (P < .003). Plasma NEDD9 level was associated with 60-day mortality (adjusted OR, 9.7; 95% CI, 1.6-60.4; P = .015). Syndecan-1 level correlated with both baseline (ρ = 0.4; P = .001) and day 3 ventilatory ratio (ρ = 0.5; P < .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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CHEST critical care
CHEST critical care Critical Care and Intensive Care Medicine, Pulmonary and Respiratory Medicine
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信