重症 COVID-19 ICU 患者肺损伤量与内质网应激表达之间的关系

Domitille Renard, Mikael Verdalle-Cazes, Perrine Leprêtre, Jérémy Bellien, Valery Brunel, S. Renet, F. Tamion, E. Besnier, T. Clavier
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摘要

SARS-CoV-2 与内质网应激(ERS)之间已经建立了联系。然而,炎症、ERS 和器官损伤体积之间的关系在人类中并不十分清楚。我们进行了一项单中心回顾性研究(前瞻性队列的辅助分析),研究对象包括重症 COVID-19 ICU 患者,他们在入院前/后 24 小时接受了胸部计算机断层扫描(CT),以评估肺损伤体积(LDV)。我们建立了两个多变量线性回归模型,以确定与入院时血浆中 78 kDa-葡萄糖调节蛋白(GRP78;ERS 标志物)和白细胞介素-6(IL-6;炎症标志物)水平相关的因素。在分析的63名患者中,GRP78血浆水平在两个多变量模型中均与LDV相关(β = 22.23 [4.08;40.38]; p = 0.0179, β = 20.47 [0.74;40.20]; p = 0.0423),但与入院时器官衰竭(序贯器官衰竭评估(SOFA)评分)无关(r = 0.03 [-0.22;0.28]; p = 0.2559)。ICU 幸存者的 GRP78 血浆水平较低(分别为 1539.4 [1139.2;1941.1] vs. 1714.2 [1555.2;2579.1] pg./mL;p = 0.0297)。在两个多变量模型中,IL-6血浆水平与入院时的SOFA评分相关(β = 136.60 [65.50;207.70]; p = 0.0003, β = 193.70 [116.60;270.90]; p < 0.0001),但与LDV无关(r = 0.13 [-0.14;0.39]; p = 0.3219)。ICU 幸存者和非幸存者的 IL-6 血浆水平没有差异(分别为 12.2 [6.0;43.7] vs. 30.4 [12.9;69.7] pg./mL;p = 0.1857)。在严重的 COVID-19 患者中,ERS 与 LDV 相关,但与全身炎症无关,而全身炎症与器官衰竭相关,但与 LDV 无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between volume of lung damage and endoplasmic reticulum stress expression among severe COVID-19 ICU patients
Links have been established between SARS-CoV-2 and endoplasmic reticulum stress (ERS). However, the relationships between inflammation, ERS, and the volume of organ damage are not well known in humans. The aim of this study was to explore whether ERS explains lung damage volume (LDV) among COVID-19 patients admitted to the intensive care unit (ICU).We conducted a single-center retrospective study (ancillary analysis of a prospective cohort) including severe COVID-19 ICU patients who had a chest computed tomography (CT) scan 24 h before/after admission to assess LDV. We performed two multivariate linear regression models to identify factors associated with plasma levels of 78 kDa-Glucose-Regulated Protein (GRP78; ERS marker) and Interleukin-6 (IL-6; inflammation marker) at admission.Among 63 patients analyzed, GRP78 plasma level was associated with LDV in both multivariate models (β = 22.23 [4.08;40.38]; p = 0.0179, β = 20.47 [0.74;40.20]; p = 0.0423) but not with organ failure (Sequential Organ Failure Assessment (SOFA) score) at admission (r = 0.03 [−0.22;0.28]; p = 0.2559). GRP78 plasma level was lower among ICU survivors (1539.4 [1139.2;1941.1] vs. 1714.2 [1555.2;2579.1] pg./mL. respectively; p = 0.0297). IL-6 plasma level was associated with SOFA score at admission in both multivariate models (β = 136.60 [65.50;207.70]; p = 0.0003, β = 193.70 [116.60;270.90]; p < 0.0001) but not with LDV (r = 0.13 [−0.14;0.39]; p = 0.3219). IL-6 plasma level was not different between ICU survivors and non-survivors (12.2 [6.0;43.7] vs. 30.4 [12.9;69.7] pg./mL. respectively; p = 0.1857). There was no correlation between GRP78 and IL-6 plasma levels (r = 0.13 [−0.13;0.37]; p = 0.3106).Among severe COVID-19 patients, ERS was associated with LDV but not with systemic inflammation, while systemic inflammation was associated with organ failure but not with LDV.
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